Skip to main content
  • AACR Publications
    • Blood Cancer Discovery
    • Cancer Discovery
    • Cancer Epidemiology, Biomarkers & Prevention
    • Cancer Immunology Research
    • Cancer Prevention Research
    • Cancer Research
    • Clinical Cancer Research
    • Molecular Cancer Research
    • Molecular Cancer Therapeutics

AACR logo

  • Register
  • Log in
  • Log out
  • My Cart
Advertisement

Main menu

  • Home
  • About
    • The Journal
    • AACR Journals
    • Subscriptions
    • Permissions and Reprints
    • Reviewing
    • CME
  • Articles
    • OnlineFirst
    • Current Issue
    • Past Issues
    • CCR Focus Archive
    • Meeting Abstracts
    • Collections
      • COVID-19 & Cancer Resource Center
      • Breast Cancer
      • Clinical Trials
      • Immunotherapy: Facts and Hopes
      • Editors' Picks
      • "Best of" Collection
  • For Authors
    • Information for Authors
    • Author Services
    • Best of: Author Profiles
    • Submit
  • Alerts
    • Table of Contents
    • Editors' Picks
    • OnlineFirst
    • Citation
    • Author/Keyword
    • RSS Feeds
    • My Alert Summary & Preferences
  • News
    • Cancer Discovery News
  • COVID-19
  • Webinars
  • Search More

    Advanced Search

  • AACR Publications
    • Blood Cancer Discovery
    • Cancer Discovery
    • Cancer Epidemiology, Biomarkers & Prevention
    • Cancer Immunology Research
    • Cancer Prevention Research
    • Cancer Research
    • Clinical Cancer Research
    • Molecular Cancer Research
    • Molecular Cancer Therapeutics

User menu

  • Register
  • Log in
  • Log out
  • My Cart

Search

  • Advanced search
Clinical Cancer Research
Clinical Cancer Research
  • Home
  • About
    • The Journal
    • AACR Journals
    • Subscriptions
    • Permissions and Reprints
    • Reviewing
    • CME
  • Articles
    • OnlineFirst
    • Current Issue
    • Past Issues
    • CCR Focus Archive
    • Meeting Abstracts
    • Collections
      • COVID-19 & Cancer Resource Center
      • Breast Cancer
      • Clinical Trials
      • Immunotherapy: Facts and Hopes
      • Editors' Picks
      • "Best of" Collection
  • For Authors
    • Information for Authors
    • Author Services
    • Best of: Author Profiles
    • Submit
  • Alerts
    • Table of Contents
    • Editors' Picks
    • OnlineFirst
    • Citation
    • Author/Keyword
    • RSS Feeds
    • My Alert Summary & Preferences
  • News
    • Cancer Discovery News
  • COVID-19
  • Webinars
  • Search More

    Advanced Search

Human Cancer Biology

Targetable Signaling Pathway Mutations Are Associated with Malignant Phenotype in IDH-Mutant Gliomas

Hiroaki Wakimoto, Shota Tanaka, William T. Curry, Franziska Loebel, Dan Zhao, Kensuke Tateishi, Juxiang Chen, Lindsay K. Klofas, Nina Lelic, James C. Kim, Dora Dias-Santagata, Leif W. Ellisen, Darrell R. Borger, Sarah-Maria Fendt, Matthew G. Vander Heiden, Tracy T. Batchelor, A. John Iafrate, Daniel P. Cahill and Andrew S. Chi
Hiroaki Wakimoto
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Shota Tanaka
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
William T. Curry
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Franziska Loebel
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Dan Zhao
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Kensuke Tateishi
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Juxiang Chen
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Lindsay K. Klofas
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Nina Lelic
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
James C. Kim
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Dora Dias-Santagata
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Leif W. Ellisen
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Darrell R. Borger
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Sarah-Maria Fendt
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Matthew G. Vander Heiden
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Tracy T. Batchelor
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
A. John Iafrate
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Daniel P. Cahill
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Andrew S. Chi
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
1Department of Neurosurgery; 2Division of Hematology/Oncology, Department of Neurology, Stephen E. and Catherine Pappas Center for Neuro-Oncology, 3Translational Research Laboratory; 4Department of Pathology; 5Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge; 6Translational Neuro-Oncology Laboratory; 7Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; 8Vesalius Research Center, VIB and Department of Oncology, KU Leuven, Leuven, Belgium
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
DOI: 10.1158/1078-0432.CCR-13-3052 Published June 2014
  • Article
  • Figures & Data
  • Info & Metrics
  • PDF
Loading

Abstract

Purpose: Isocitrate dehydrogenase (IDH) gene mutations occur in low-grade and high-grade gliomas. We sought to identify the genetic basis of malignant phenotype heterogeneity in IDH-mutant gliomas.

Methods: We prospectively implanted tumor specimens from 20 consecutive IDH1-mutant glioma resections into mouse brains and genotyped all resection specimens using a CLIA-certified molecular panel. Gliomas with cancer driver mutations were tested for sensitivity to targeted inhibitors in vitro. Associations between genomic alterations and outcomes were analyzed in patients.

Results: By 10 months, 8 of 20 IDH1-mutant gliomas developed intracerebral xenografts. All xenografts maintained mutant IDH1 and high levels of 2-hydroxyglutarate on serial transplantation. All xenograft-producing gliomas harbored “lineage-defining” mutations in CIC (oligodendroglioma) or TP53 (astrocytoma), and 6 of 8 additionally had activating mutations in PIK3CA or amplification of PDGFRA, MET, or N-MYC. Only IDH1 and CIC/TP53 mutations were detected in non–xenograft-forming gliomas (P = 0.0007). Targeted inhibition of the additional alterations decreased proliferation in vitro. Moreover, we detected alterations in known cancer driver genes in 13.4% of IDH-mutant glioma patients, including PIK3CA, KRAS, AKT, or PTEN mutation or PDGFRA, MET, or N-MYC amplification. IDH/CIC mutant tumors were associated with PIK3CA/KRAS mutations whereas IDH/TP53 tumors correlated with PDGFRA/MET amplification. Presence of driver alterations at progression was associated with shorter subsequent progression-free survival (median 9.0 vs. 36.1 months; P = 0.0011).

Conclusion: A subset of IDH-mutant gliomas with mutations in driver oncogenes has a more malignant phenotype in patients. Identification of these alterations may provide an opportunity for use of targeted therapies in these patients. Clin Cancer Res; 20(11); 2898–909. ©2014 AACR.

This article is featured in Highlights of This Issue, p. 2815

Translational Relevance

Recurrent mutations in the isocitrate dehydrogenase 1 (IDH1) and IDH2 genes identify gliomas with a better prognosis. However, most IDH-mutant gliomas eventually transform to more aggressive tumors and become fatal. The genetic events that drive this later malignant behavior are largely unknown. Here, we find that a subset of IDH-mutant gliomas acquire mutations in cancer driver genes when they recur. Presence of these mutations is associated with more rapid subsequent progression. We also find that genetic subtypes of IDH-mutant gliomas utilize distinct oncogenic pathways during transformation to more malignant tumors. Moreover, IDH-mutant gliomas with driver mutations preferentially establish orthotopic xenograft tumors in mouse brain and are sensitive to targeted inhibition of the mutant gene product. Identification of targetable recurrent driver mutations provides novel therapeutic possibilities for the patients with IDH-mutant glioma who are most in need of new treatments.

Introduction

Shortly after the discovery of recurrent mutations in the isocitrate dehydrogenase 1 (IDH1) and IDH2 genes, it was recognized that IDH-mutant diffuse gliomas have a clinical phenotype distinct from IDH-wild-type gliomas (1–5). More recently, 2 major genetic subtypes of IDH-mutant glioma have been identified: one genetic lineage is defined by TP53 and α thalassemia/mental retardation syndrome x-linked (ATRX) mutations and strong correlation with astrocytic histology (1, 2, 5, 6), and a second lineage is characterized by concurrent mutations in homolog of Drosophila capicua (CIC), Far Upstream Element Binding Protein (FUBP1), and the telomerase reverse transcriptase (TERT) promoter as well as tight association with 1p/19q codeletion and oligodendroglioma histopathology (2, 5, 7–12). Notably, the genomic alterations that frequently occur in the more common IDH-wild-type primary glioblastoma (GBM; WHO grade IV), including EGFR gene amplification and rearrangement, PTEN mutation, and CDKN2A-CDKN2B deletion, are rare in IDH-mutant gliomas (2, 5, 12, 13). Thus, IDH-mutant gliomas are thought to arise via a molecular pathway that is distinct from primary GBM (5, 6).

Although IDH-mutant diffuse gliomas carry a relatively better prognosis (1–4), most ultimately transform to a more malignant phenotype and become lethal. A fundamental paradigm in cancer progression imparts that morphologic changes during the process of malignant transformation reflect the sequential acquisition of genetic alterations (14). IDH1/2 mutation and widespread hypermethylation of CpG islands (CpG island hypermethylator phenotype or CIMP) are the earliest known events in glioma development, preceding the “lineage-defining” acquisition of TP53 mutation in astrocytomas or 1p/19q codeletion in oligodendrogliomas (5, 10, 15–18). Mutant IDH1/2 represents a “trunk” mutation (19) in the molecular evolutionary tree of gliomas because it is ubiquitously present throughout the tumor cell mass (15, 20) and retained on progression from low- to high-grade with few exceptions (2, 10, 15, 20, 21). The lineage-defining or “secondary” genetic alterations in IDH-mutant gliomas (TP53/ATRX mutations or 1p/19q codeletion/CIC mutations) are also early events in tumor development, as they are present in the vast majority of low-grade (WHO grade II) diffuse gliomas (2, 12). Therefore, “primary” IDH1/2 mutation and “secondary” genetic alterations are unlikely to be the triggers of more malignant behavior. A few genetic alterations have been reported to be associated with higher grade or progressive IDH-mutant gliomas, however the alterations that drive transformation to a more malignant phenotype remain largely unknown (2, 5, 13, 15).

One limitation in the study of IDH-mutant glioma has been the scarcity of experimental models harboring endogenous IDH1/2 mutation. Successful propagation of tumor-initiating cells (TIC), cancer cells that display stem cell properties, and generation of intracerebral glioma xenografts from IDH-mutant patient gliomas are rare (22–25). The reasons for the difficulty in establishing models from patient IDH-mutant gliomas are unknown.

Herein, we hypothesized that additional “tertiary” genetic alterations, which have been noted to occur in IDH-mutant gliomas (7, 15, 26, 27), could be the drivers of the progressive malignant phenotype of IDH-mutant gliomas. We therefore tested 20 consecutive IDH-mutant glioma specimens from patients undergoing surgery at our institution for the ability to establish intracerebral xenografts in mice. We performed a comparative genetic analysis of all primary tumor specimens using a CLIA-certified molecular panel and discovered that the IDH-mutant gliomas that successfully established orthotopic xenografts (8 tumors) were enriched with additional tertiary oncogenic genetic alterations, including PIK3CA mutation and amplification of the PDGFRA, MET, and N-MYC genes. IDH-mutant glioma TICs generated from xenograft-forming tumors exhibit oncogenic addiction to tertiary mutations. In patients with IDH-mutant glioma, tertiary alterations seem to be acquired at the time of tumor progression and also associated with higher pathologic grade and shorter progression-free survival (PFS). These data indicate acquisition of tertiary alteration is associated with more aggressive tumor behavior and may predict the ability to establish intracerebral xenografts in mice.

Materials and Methods

Biologic samples and clinical data

From September 2011 to October 2012, we prospectively accrued 20 consecutive untreated (9 patients) and previously treated (11 patients) patients with IDH-mutant glioma undergoing resection at the Massachusetts General Hospital (MGH). Patients either had previously confirmed IDH mutation or were accrued if clinical suspicion of IDH-mutant glioma was high based on characteristic features such as young age, frontal location, and lesser degree of contrast enhancement and necrosis on neuroimaging (5). Progression of disease was confirmed by either tissue diagnosis or standard response criteria (28). All tumor samples and clinical information were collected under MGH institutional review board approved protocols, and informed consent was obtained from all patients. All mouse procedures were approved by the Subcommittee on Research Animal Care at MGH.

Glioma neurospheres and orthotopic xenografts

Fresh surgical specimens were enzymatically dissociated, and 2 to 5 × 104 cells were stereotactically implanted into the right striatum of the brains of 7- to 10-week-old female severe combined immunodeficient mice as described (29). In some cases when an excess of tumor tissue was available, cells were briefly cultured in neurosphere medium as described (30) to enrich for TIC neurospheres, and a similar number of cells were implanted within 48 hours of in vitro culture. There was no notable difference in xenograft formation with either method. Mice were monitored for status twice per week and sacrificed when neurologic deficits became significant. A minimum 10-month observation period after implantation was required to determine whether orthotopic xenografts developed, although all animals were sacrificed after 1 year to assess for tumor formation. Brains were removed for pathologic studies and tumors were excised to re-establish TIC neurosphere cultures. TICs were then either implanted into the brains of new mice or used for in vitro assays as described (29, 31).

Histology and immunostaining

Hematoxylin and eosin staining and immunohistochemistry (IHC) were performed on formalin-fixed paraffin-embedded (FFPE) sections as described (29, 31). Primary antibodies used for IHC were anti-IDH1 R132H (Dianova; 1:100), Ki-67 (MIB-1; Dako; 1:150), anti-CD31 (BD Pharmingen; 1:150), and anti-nestin (Santa Cruz; 1:400).

Genotyping and FISH data

Clinical molecular profiling was performed as described (32, 33). Briefly, the MGH SNaPshot assay is a multiplexed, PCR-based, single-base extension assay that interrogates 73 commonly mutated loci from 23 genes (AKT1, APC, BRAF, CTNNB1, EGFR, EML4-ALK, HER2, FGFR3, GNA11, GNAQ, GNAS, HRAS, IDH1, IDH2, KIT, KRAS, MEK1, NOTCH1, NRAS, PIK3CA, PTEN, RET, TP53). Genomic PCR-based sequencing was used to sequence all coding exons of the IDH1, CIC, TP53, PIK3CA, and PIK3R1 genes. PCR products were amplified from genomic DNA templates with Platinum Taq polymerase per manufacturer's protocol using intron-based primers spanning the expressed coding sequences (Supplementary Table S2) then Sanger sequenced (Beckman Coulter Genomics). FISH assays for the EGFR, MET, and PDGFRA genes were performed using BAC probes CTD-2113A18 (7p EGFR locus), CTB-13N12 (7q MET locus), CEP7 (centromere 7 control), RP11-58C6 (4q PDGFRA locus), and CEP4 (centromere 4 control) (Abbott) as described (32). BAC clone RP11-480N14 (chr2: 15991148-16158895) was used to make the N-MYC probe and ALK (2p23) Proximal Probe (Kreatech) was used for centromere 2 control. Gene/control probe copy number ratios of >2.0 were considered amplified. 1p and 19q status was determined using the Vysis 1p36/1q25 and 19q13/19p13 FISH Probe Kit (Abbott). 1p/1q and 19q/19p ratios of <0.75 were considered loss and >0.75 as maintained.

Gas chromatography-mass spectroscopy data

Ten to 20 mg of frozen tumor tissue was homogenized and extracted with methanol/chloroform. Metabolites were derivatized with N-(tert-butyldimethylsilyl)-N-methyl-trifluoroacetamide, with 1% tert-butyldimethylchlorosilane (Sigma) and analyzed on a 6890N GC system (Agilent Technologies) combined with a 5975B Inert XL MS system (Agilent Technologies). 2-Hydroxyglutarate (2HG) fragment 433 m/z and the glutamate fragment 432 m/z were used for further analysis (34). 2HG and glutamate concentrations were normalized to the internal standard norvaline and tissue weight as described (35).

In vitro drug and shRNA inhibition studies

Dissociated TICs were seeded to 96-well plates at 7,000 to 8,000 cells per well. Serially diluted inhibitor was added to wells, and cells were further cultured for 5 days. Viability of cells was measured by CellTiter-Glo assay (Promega) and the EC50 values were determined. All in vitro inhibitor assays were performed on TICs within 5 passages from dissociation from tumor. JQ1 and BYL719 were gifts from J.E. Bradner and J.A. Engelman, respectively. Crizotinib and sunitinib were obtained from Selleck Chemicals.

To knockdown N-myc expression, lentivirus vectors carrying shRNA for N-MYC (Sigma, pLKO.1) were packaged using ScreenFect (Wako)-mediated cotransfection of vector and packaging plasmid DNAs to 293T cells. MGG152 cells were infected with lentivirus in the presence of polybrene (6 μg/mL), selected with puromycin (0.5 μg/mL) for 3 days, and silencing confirmed with Western blot analysis. Cell viability and sphere formation were assessed 7 days later.

Statistical analyses

Statistical analysis was performed with JMP software. For parametric analyses, 2-tailed t tests were used and for analysis of frequencies of nominal data, 2-tailed Fisher exact test was used. Data are expressed as mean + SD. Survival was analyzed by the Kaplan–Meier method with 2-sided log-rank statistics.

Results

Establishment of intracerebral xenografts with endogenous IDH mutation

We studied the potential of 20 serially collected patient IDH1-mutant glioma specimens to form xenograft after stereotactic implantation in immunocompromised mouse brains. Two tumors were low-grade (WHO grade II), 10 were anaplastic (WHO grade III), and 8 were GBMs, of which 3 were “secondary” GBMs that had transformed from a known lower-grade glioma (Table 1). All 20 gliomas in our study had IDH1 mutations, which occur far more frequently than IDH2 mutations in gliomas (2, 36). In parallel, we cultured TIC-enriched cells using the neurosphere system.

View this table:
  • View inline
  • View popup
Table 1.

Orthotopically implanted patient IDH-mutant gliomas

Notably, 8 of 20 IDH-mutant glioma tumors generated intracerebral xenografts, with the time to lethal xenograft ranging between 1 and 7 months (Fig. 1), Table 1 and Supplementary Fig. S1). All xenografts closely recapitulated parent human tumor phenotypes histologically (Fig. 1; Supplementary Figs. S1–S3, and Table 1). In vitro proliferation of the different lines varied, with doubling times ranging from 2.5 days (MGG152) to 10 days (MGG79, MGG108, MGG132). All lines could be passaged for at least 5 passages, however 2 lines (MGG119, MGG152) could be stably cultured for at least 4 months. All xenografts harbored endogenous IDH1 R132H mutation and retained the mutant allele upon serial passage in vitro or serial transplantation in orthotopic xenograft (Supplementary Figs. S4 and S5). Orthotopic xenografts were confirmed by GC-MS to have high-level production of the mutant-specific metabolite, 2HG (Supplementary Table S1).

Figure 1.
  • Download figure
  • Open in new tab
  • Download powerpoint
Figure 1.

Mouse orthotopic xenografts generated from patient IDH1 R132H-mutant gliomas. A, rows: individual IDH1-mutant glioma orthotopic (intracerebral) xenografts. Columns left to right: xenograft line and patient tumor histology; representative patient MRI (yellow arrows highlight areas of tumor); gross xenograft histologic hematoxylin and eosin (HE) section; microscopic xenograft HE section; gross xenograft IHC section stained with IDH1 R132H mutant-specific antibody (brown); microscopic xenograft anti-IDH1 R132H (brown) IHC. Predominantly nodular (MGG60, 152) and infiltrative (MGG79, 117) growth patterns of xenografts are in accordance with the respective human tumors as demonstrated by MRI. B and C, microscopic section of MGG117 primary tumor (B) and orthotopic xenograft (C) showing marked cellular heterogeneity and nuclear pleomorphism in both sections. D and E, MGG60 xenograft demonstrating tumor angiogenesis by (D) HE and (E) endothelium-specific anti-CD31 antibody IHC. GBM-O, GBM with oligodendroglial component; Rec AOA, recurrent anaplastic oligoastrocytoma; Sec GBM, secondary GBM; GBM-PNET, GBM with primitive neuroectodermal tumor component.

Genetic alterations associated with ability to generate intracerebral xenograft

We sought to identify the mechanisms accounting for the ability to generate orthotopic xenograft in our set of IDH-mutant gliomas. There was no clear distinction in host factors such as patient age, sex, or prior treatment (radiation or various combinations of radiation and different chemotherapies; Table 1) between gliomas that formed orthotopic xenograft versus those that did not. Generally, tumors that were able to form xenografts had GBM (WHO grade IV) histology (6/8 xenografts vs. 2/12 in the non–xenograft-forming subset) and lacked 1p/19q codeletion (7/8 xenografts).

We conducted a comparative genetic analysis on the primary tumor specimens to assess whether additional oncogenic alterations might account for differences in the ability to generate xenograft. All 8 xenograft-forming tumors and 10 of 12 non–xenograft-forming tumors harbored the IDH1 R132H variant, which accounts for ∼90% of the IDH1 mutations in gliomas (2, 12, 36), and the remaining 2 non–xenograft-forming gliomas harbored IDH1 R132C. Interestingly, one glioma xenograft (MGG79) was homozygous for IDH1 R132H mutation and the corresponding orthotopic xenograft produced high levels of 2HG (Supplementary Fig. S4 and Table S1). This finding is in contrast with a previous report suggesting a wild-type IDH1 allele is necessary for 2HG production (37).

Focused genotyping analysis of all implanted primary tumors was conducted with our CLIA-certified clinical molecular profiling platform (32), which surveys 25 commonly mutated cancer-associated genes. We specifically assessed for “tertiary” genetic alterations, which we defined as nonlineage mutations, because lineage-associated mutations (astrocytic ATRX/TP53 mutations or oligodendroglial CIC/TERT mutations and 1p/19q codeletion) occur in virtually all low-grade IDH-mutant gliomas. Strikingly, 6 of 8 xenograft-forming tumors harbored tertiary mutations whereas none were detected in non–xenograft-forming patient gliomas (P = .0007; Table 1).

The detected tertiary alterations included hotspot-activating mutations in PIK3CA (2/6) and high-level focal amplifications in the PDGFRA (2/6) and MET (1/6) genes (Table 1). In addition, we sequenced the entire coding regions of PIK3CA, which encodes p110α, and PIK3R1, which encodes the phosphoinositide 3-kinase (PI3K) regulatory subunit p85α, in all xenograft-forming tumors and detected no other mutations. Notably, one GBM had focal primitive neuroectodermal tumor (PNET) histopathology (MGG152; Fig. 1A) and was unusually malignant in both the patient (5-month overall survival) and in orthotopic xenograft (lethal within 1 month; Table 1). A previous study detected C-MYC or N-MYC amplification in a significant proportion of malignant gliomas-harboring PNET-like components (38); therefore, we interrogated these genes in MGG152 and identified high-level N-MYC amplification (Fig. 2A). We confirmed that all the tertiary genetic alterations detected in the primary tumors were maintained in the respective orthotopic xenografts (Fig. 2A), suggesting these mutations play a role in the tumor initiating capability of IDH1-mutant gliomas.

Figure 2.
  • Download figure
  • Open in new tab
  • Download powerpoint
Figure 2.

Recurrent tertiary genetic alterations in IDH-mutant gliomas drive tumor cell growth. A, FISH images of primary tumors (left column) and corresponding orthotopic xenografts (right column). Top row, MGG117 probed with PDGFRA (red) and CEN4 control (green). Second row, MGG132 primary tumor (left) probed with MET (green) and CEN7 control (red) and xenograft (right) probed with MET (red) and CEN7 (green). Third row, MGG152 probed with N-MYC (orange) and 2p23 control (green). Bottom row, sequencing traces of the PIK3CA R93 locus with wild-type (black trace) and mutant (green trace, red arrow) alleles. Left: PIK3CA wild-type primary tumor (control). Middle, MGG108 primary tumor. Right, MGG108 TICs. B, effect of BYL719 and JQ1 on MGG108 and MGG152 TICs. Asterisk, MGG108 (PIK3CA mutant) and MGG152 (N-MYC amplified) at 10 μmol/L of BYL719 (P = 0.004, t test). C, N-Myc knockdown in MGG152 TICs. MGG152 was infected with lentivirus carrying N-MYC shRNA or empty vector. Upper left, Western blot analysis of TICs using antibodies against N-myc and vinculin (loading control). Lower left: cell viability assays of TICs expressing N-MYC shRNA or empty vector. Right, TIC neurospheres infected with lentivirus carrying empty (upper) or N-MYC shRNA (lower).

Tertiary genetic alterations are drivers in IDH-mutant glioma xenografts

We then tested the effect of small molecule inhibitors targeted at the identified tertiary mutations on in vitro proliferation. We examined the impact of BYL719, a highly selective inhibitor of p110α (39), on the viability of MGG108 (PIK3CA R93Q) and MGG152 (PIK3CA/PIK3R1 wild type) TICs. We observed more potent inhibition of MGG108 than MGG152 cells (IC50 = 7.5 μmol/L for MGG108 vs. 20.1 μmol/L for MGG152), indicating PIK3CA mutation functions as a driver of proliferation in MGG108 cells (Fig. 2B). We then examined the effect of the Myc pathway small molecule inhibitor JQ1 (40) in MGG108 and MGG152 (N-MYC amplified). As expected, MGG152 was significantly more sensitive to JQ1 in cell viability assays relative to MGG108, which lacks N-MYC or C-MYC amplification (IC50 = 0.04 μmol/L for MGG152 vs. 2.08 μmol/L for MGG108; Fig. 2B). Furthermore, shRNA knockdown of N-myc expression in MGG152 suppressed cell proliferation and nearly eliminated sphere formation ability (Fig. 2C and Supplementary Fig. S6). We also tested sunitinib and crizotinib, small molecule inhibitors of PDGFR and c-Met, respectively, in several lines with known PDGFRA and MET copy number status. We found that sunitinib was more potent against a line with high-level PDGFRA amplification (MGG117) than those without (MGG108 and MGG119), whereas crizotinib was most effective in a line harboring MET amplification (MGG132) (Supplementary Fig. S7). These data suggest that tertiary alterations are oncogenic drivers in IDH-mutant glioma xenografts.

Acquisition of tertiary mutations during malignant transformation

We then asked whether tertiary alterations are acquired when lower-grade IDH-mutant gliomas progress or transform to higher grade tumors in patients. We examined our dataset of 149 patients with IDH-mutant glioma who had clinical molecular profiling at our center and identified 20 tumors with tertiary alterations (13.4%). Tertiary alterations were nearly exclusively present in progressive low-grade (WHO grade II) or high-grade (WHO grade III or IV) tumors (Table 2); specifically 6 grade II (4 progressive), 6 grade III, and 8 grade IV tumors. Presence of a tertiary mutation was associated with grade IV (GBM) versus lower grade (grade II or III) histology (P = 0.027).

View this table:
  • View inline
  • View popup
Table 2.

Genetic alterations in IDH-mutant glioma patients at MGH

We then analyzed a subset of 56 patients who underwent biopsy and genotyping at the time of radiographically defined disease progression. Presence of tertiary alteration in the progressive tumor (14 patients, 25%) was associated with significantly shorter subsequent PFS (median 9.0 months; 95% CI, 4.4–49.3, with tertiary alteration versus 36.1 months; 95% CI, 18.7–52.8, without, P = 0.0011; Fig. 3A and B). Notably, there was no difference in PFS from the time of initial diagnosis (median 55.6 months; 95% CI, 24.6- 93.1, with tertiary alteration vs. 54.1 months; 95% CI, 35.7–73.0, without, P = 0.76; Fig. 3A), implicating the tertiary alteration detected at progression as the driver of malignant degeneration in these patients. There was no detectable difference in overall survival; however, there were few deaths in either group (13/56 total patients), therefore longer follow-up time is needed to assess this endpoint.

Figure 3.
  • Download figure
  • Open in new tab
  • Download powerpoint
Figure 3.

Tertiary alterations are acquired at progression and reduce subsequent PFS. A and B, Kaplan–Meier estimates of PFS in patients who had biopsy at initial diagnosis and at progression by presence of tertiary alteration. A, PFS from the time of initial diagnosis and B, from the time of progression. C, SNaPshot and FISH images of matched patient tumors. Top left, SNaPshot images of patient 8 reveal wild-type PIK3CA E545 genotype in the initial tumor and PIK3CA E545K mutant allele (red arrow) in the progressive tumor (8-P). Bottom left, FISH images of patient SA initial and progressive (SA-P) tumor with PDGFRA probe (red) and CEN4 control probe (green). Top right, FISH images of patient 19 initial and progressive tumor (19-P) probed for PDGFRA (red) and CEN4 (green). Bottom right, patient 14 initial and progressive (14-P) tumor probed with MET (green) and CEN7 control (red).

Several tertiary genetic events were recurrently identified (Table 2), including activating mutations in PIK3CA (9 tumors) and KRAS (4 tumors) and PDGFRA amplification (4 tumors). PIK3CA and KRAS mutations were most often detected in tumors with at least a component of oligodendroglioma histology (7/9 PIK3CA mutant and 3/4 KRAS mutant tumors). Interestingly, all 4 PDGFRA-amplified tumors were purely astrocytic (P = 0.026). When specific oncogenes were compared by IDH genetic lineage rather than histopathology (within the set of tumors with tertiary mutations and confirmed lineage mutations), we identified significant associations between 1p/19q codeleted tumors and intracellular signaling pathway gene mutations (KRAS or PIK3CA, P = 0.002) and between receptor tyrosine kinase amplification (PDGFRA or MET) and non–1p/19q codeleted (TP53 mutant) tumors (P = 0.029).

To assess whether tertiary alterations are acquired at tumor progression, we examined paired tumor specimens from newly diagnosed and progressive tumors from 6 patients in whom we detected tertiary mutations. For 2 patients with PDGFRA amplification and 1 patient with focal MET amplification, we confirmed these alterations were present in the progressive but not in the initial tumor specimens (Fig. 3C). In 2 of 3 patients with PIK3CA mutant, the PIK3CA mutations were present only in the progressive tumor (Fig. 3C). The third patient (Patient 6 in Table 2) had PIK3CA E545G mutation in both the diagnostic and progressive tumor specimens. This patient was treated with 12 cycles of temozolomide and progressed just 24.6 months after diagnosis, a relatively rapid time to progression for low-grade oligodendrogliomas with 1p/19q codeletion.

Discussion

IDH-mutant diffuse gliomas nearly always progress after radiation therapy and chemotherapy and eventually transform to more malignant tumors. Effective therapeutic options at that stage are lacking. Herein we demonstrate that the subset of IDH-mutant gliomas that acquire an aggressive phenotype late in the disease are driven by specific tertiary oncogenic alterations. These tertiary alterations are associated with more malignant tumors in patients and increased tumor-forming ability in mice. Importantly, these tertiary alterations represent potential therapeutic targets for patients with IDH-mutant gliomas who are most in need of treatment.

Our data suggest that after acquisition of lineage-defining mutations, IDH-mutant gliomas may follow multiple pathways to transformation (Fig. 4). 1p/19q codeleted tumors tend to activate the PI3K/mTOR or Ras intracellular signaling pathways and TP53-mutant tumors tend to amplify growth factor receptor tyrosine kinases. Our findings are consistent with prior reports; recurrent PIK3CA mutations have been detected in a subset of IDH-mutant, 1p/19q codeleted anaplastic oligodendrogliomas (7, 26) and 2 recent reports observed enrichment of PDGFRA amplification in IDH-mutant versus IDH-wild-type primary GBM (27, 41). In addition, we find that activation of N-myc may be a particularly malignant transformation pathway in IDH-mutant glioma. A recent study similarly observed a correlation between c-Myc expression and shorter time to transformation within IDH-mutant gliomas (42). Together with these reports, our data suggests IDH-mutant gliomas may undergo a sequenced genetic evolution analogous to IDH2-mutant acute myeloid leukemia, where stepwise acquisition of distinct classes of mutations results in more aggressive disease (43).

Figure 4.
  • Download figure
  • Open in new tab
  • Download powerpoint
Figure 4.

Molecular taxonomy of IDH-mutant glioma progression. We propose that IDH-mutant gliomas develop and progress through an ordered sequence of oncogenic alterations. IDH-mutant gliomas are initiated by the occurrence of IDH1 or IDH2 mutation and widespread hypermethylation of CpG islands (CpG island methylator phenotype, CIMP) in a glial progenitor cell population. The subsequent acquisition of TP53 and ATRX mutations results in development along an astrocytoma pathway, whereas the codeletion of 1p and 19q (t1;19) along with CIC, FUBP1, and TERT mutations result in the formation of oligodendrogliomas. After acquisition of these “lineage-defining” mutations, IDH-mutant astrocytomas and oligodendrogliomas may follow several “tertiary” genetic pathways during the transformation to malignant or high-grade tumors. Astrocytomas tend to amplify growth factor receptor genes such as PDGFRA and MET, whereas oligodendrogliomas tend to develop activating mutations in intracellular signaling genes such as PIK3CA and KRAS. Alternative tertiary pathways include Myc activation and other undescribed mutations. Acquisition of tertiary genetic alterations may result in more malignant behavior. RTK, receptor tyrosine kinase; MAPK, mitogen-activated protein kinase.

The mechanisms by which IDH-mutant gliomas acquire tertiary mutations are largely unknown. A recent study observed that a subset of IDH-mutant low-grade gliomas developed a hypermutation phenotype (15, 44) after treatment with temozolomide. All of the hypermutated gliomas in their dataset harbored driver mutations, many in the PI3K/mTOR signaling pathway (15). In our dataset, 10 of 20 patients with tertiary mutation were previously treated with alkylating chemotherapy (Table 2). Five of our 10 chemotherapy-treated patients had PI3K/mTOR pathway mutations in their tumors, and interestingly one tumor had activating mutations in 3 oncogenes (PIK3CA, AKT, and KRAS), suggesting it may be hypermutated. However, 9 patients as well as 2 xenograft-forming tumors from our implantation study harbored tertiary alterations and had no prior treatment, indicating that genomic instability resulting from DNA-damaging therapy is not the sole evolutionary path to malignant progression in IDH-mutant gliomas. The drivers of tertiary mutation in untreated IDH-mutant tumors remain to be determined.

The overall frequency of tertiary mutations in our dataset was 13.4%, which may be reflective of the focused nature of our genotyping panel. Our data suggests resampling of tumor specimens at the time of progression may increase detection frequencies. We also provide rationale for sampling tumor specimens throughout the course of disease as the acquired tertiary mutation may present an opportunity for therapeutic targeting. Future genomic profiling studies that also include paired tumor samples will address important remaining questions including the scope and frequency of recurrent tertiary mutations, the timing of their appearance and the mechanisms that drive their development. Of note, our genotyping panel did not interrogate many genes commonly mutated in gliomas, such as CDK4/6, MDM2, CCND2, AKT3, RB, PARK2, and NF1 (1, 45). However, these mutations were detected in datasets consisting mostly of IDH-wild-type gliomas that evolve along a distinct molecular pathway.

By identifying recurrent, functionally significant tertiary genetic alterations, we set the stage for targeted therapy in IDH-mutant gliomas. Pharmacologic inhibitors for all of the tertiary alterations identified in our work are in development. Notably, our data suggests PDGFRA amplification warrants investigation in TP53-mutant, IDH-mutant gliomas. Outcomes for this subgroup are poor relative to the 1p/19q codeleted subtype (6) possibly because of the uncertain efficacy of chemotherapy in these tumors given their lack of 1p/19q codeletion (46, 47). We detected recurrent mutations in KRAS, which have been reported to be rare in glial tumors (45, 48, 49). Recent clinical data suggest that cancers driven by KRAS mutation may be sensitive to MEK inhibitors (50). In addition, our data suggests investigation of Myc pathway inhibitors (40) may be justified for particularly aggressive IDH-mutant gliomas, because these may harbor C-MYC or N-MYC amplification or inappropriate c-Myc expression. Analogously, a recent study reported that Myc pathway inhibition potently reduces viability of acute myeloid leukemia cells driven by mutant IDH2 (43).

Finally, development of anticancer agents in IDH-mutant gliomas has been limited by the scarcity of biologically accurate preclinical models that are serviceable for testing therapeutics. We have established a panel of endogenous IDH-mutant intracerebral glioma xenografts that represent a powerful platform for studying IDH-mutant tumor biology and for answering fundamental questions about treatment of IDH-mutant gliomas. Future work utilizing these orthotopic xenografts may help determine the optimal therapeutic strategy for IDH-mutant gliomas, which may involve inhibition of mutant IDH1, inhibition of tertiary genetic alterations, alteration of metabolic or epigenetic pathways, or a combination thereof.

Disclosure of Potential Conflicts of Interest

D. Dias-Santagata, L.W. Ellisen, and D.R. Borger are consultant/advisory board members for BioReference Laboratories Inc. M. Vander Heiden has ownership interest (including patents) in and is a consultant/advisory board member for Agios Pharmaceuticals. T.T. Batchelor reports receiving commercial research grants from Argenus, AstraZeneca, Kirin, Merck, Millennium, Novartis, Pfizer, Roche, and Spectrum. No potential conflicts of interest were disclosed by the other authors.

Authors' Contributions

Conception and design: H. Wakimoto, W.T. Curry, K. Tateishi, D.R. Borger, T.T. Batchelor, A.J. Iafrate, D.P. Cahill, A.S. Chi

Development of methodology: H. Wakimoto, K. Tateishi, L.K. Klofas, L.W. Ellisen, D.R. Borger, A.J. Iafrate, A.S. Chi

Acquisition of data (provided animals, acquired and managed patients, provided facilities, etc.): H. Wakimoto, S. Tanaka, F. Loebel, D. Zhao, K. Tateishi, J. Chen, N. Lelic, J.C. Kim, D. Dias-Santagata, S.-M. Fendt, T.T. Batchelor, A.J. Iafrate, A.S. Chi

Analysis and interpretation of data (e.g., statistical analysis, biostatistics, computational analysis): H. Wakimoto, W.T. Curry, F. Loebel, D. Zhao, L.K. Klofas, N. Lelic, L.W. Ellisen, S.-M. Fendt, A.J. Iafrate, A.S. Chi

Writing, review, and or revision of the manuscript: H. Wakimoto, S. Tanaka, W.T. Curry, F. Loebel, D. Zhao, L.K. Klofas, D. Dias-Santagata, L.W. Ellisen, D.R. Borger, S.-M. Fendt, M.G. Vander Heiden, T.T. Batchelor, A.J. Iafrate, D.P. Cahill, A.S. Chi

Administrative, technical, or material support (i.e., reporting or organizing data, constructing databases): H. Wakimoto, S. Tanaka, K. Tateishi, L.K. Klofas, N. Lelic, T.T. Batchelor, A.J. Iafrate

Study supervision: H. Wakimoto, W.T. Curry, M.G. Vander Heiden, D.P. Cahill, A.S. Chi

Grant Support

This work was supported by the American Cancer Society Institutional Research Grant and Richard B. Simches Scholars Award (A.S. Chi), Burroughs-Wellcome Career Award (D.P. Cahill), and The Koch Institute Dana Farber/Harvard Cancer Center Bridge Project (H. Wakimoto, A.S. Chi, D.P. Cahill and M.G. Vander Heiden).

The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

Acknowledgments

The authors thank Alona Muzikansky for assistance with the biostatistical analysis.

Footnotes

  • Note: Supplementary data for this article are available at Clinical Cancer Research Online (http://clincancerres.aacrjournals.org/).

  • Received November 6, 2013.
  • Revision received March 27, 2014.
  • Accepted March 28, 2014.
  • ©2014 American Association for Cancer Research.

References

  1. 1.↵
    1. Parsons D,
    2. Jones S,
    3. Zhang X,
    4. Lin J,
    5. Leary R,
    6. Angenendt P,
    7. et al.
    An integrated genomic analysis of human glioblastoma multiforme. Science 2008;321:1807–12.
    OpenUrlAbstract/FREE Full Text
  2. 2.↵
    1. Yan H,
    2. Parsons D,
    3. Jin G,
    4. McLendon R,
    5. Rasheed B,
    6. Yuan W,
    7. et al.
    IDH1 and IDH2 mutations in gliomas. N Engl J Med 2009;360:765–73.
    OpenUrlCrossRefPubMed
  3. 3.↵
    1. Houillier C,
    2. Wang X,
    3. Kaloshi G,
    4. Mokhtari K,
    5. Guillevin R,
    6. Laffaire J,
    7. et al.
    IDH1 or IDH2 mutations predict longer survival and response to temozolomide in low-grade gliomas. Neurology 2010;75:1560–6.
    OpenUrlCrossRef
  4. 4.↵
    1. Hartmann C,
    2. Hentschel B,
    3. Wick W,
    4. Capper D,
    5. Felsberg J,
    6. Simon M,
    7. et al.
    Patients with IDH1 wild type anaplastic astrocytomas exhibit worse prognosis than IDH1-mutated glioblastomas, and IDH1 mutation status accounts for the unfavorable prognostic effect of higher age: implications for classification of gliomas. Acta Neuropathol 2010;120:707–18.
    OpenUrlCrossRefPubMed
  5. 5.↵
    1. Lai A,
    2. Kharbanda S,
    3. Pope WB,
    4. Tran A,
    5. Solis OE,
    6. Peale F,
    7. et al.
    Evidence for sequenced molecular evolution of IDH1 mutant glioblastoma from a distinct cell of origin. J Clin Oncol 2011;29:4482–90.
    OpenUrlAbstract/FREE Full Text
  6. 6.↵
    1. Jiao Y,
    2. Killela PJ,
    3. Reitman ZJ,
    4. Rasheed AB,
    5. Heaphy CM,
    6. de Wilde RF,
    7. et al.
    Frequent ATRX, CIC, and FUBP1 mutations refine the classification of malignant gliomas. Oncotarget 2012;3:709–22.
    OpenUrlPubMed
  7. 7.↵
    1. Bettegowda C,
    2. Agrawal N,
    3. Jiao Y,
    4. Sausen M,
    5. Wood LD,
    6. Hruban RH,
    7. et al.
    Mutations in CIC and FUBP1 contribute to human oligodendroglioma. Science 2011;333:1453–5.
    OpenUrlAbstract/FREE Full Text
  8. 8.↵
    1. Yip S,
    2. Butterfield YS,
    3. Morozova O,
    4. Chittaranjan S,
    5. Blough MD,
    6. An J,
    7. et al.
    Concurrent CIC mutations, IDH mutations, and 1p/19q loss distinguish oligodendrogliomas from other cancers. J Pathol 2012;226:7–16.
    OpenUrlCrossRefPubMed
  9. 9.↵
    1. Killela PJ,
    2. Reitman ZJ,
    3. Jiao Y,
    4. Bettegowda C,
    5. Agrawal N,
    6. Diaz LA Jr..,
    7. et al.
    TERT promoter mutations occur frequently in gliomas and a subset of tumors derived from cells with low rates of self-renewal. Proc Natl Acad Sci U S A 2013;110:6021–6.
    OpenUrlAbstract/FREE Full Text
  10. 10.↵
    1. Watanabe T,
    2. Nobusawa S,
    3. Kleihues P,
    4. Ohgaki H
    . IDH1 mutations are early events in the development of astrocytomas and oligodendrogliomas. Am J Pathol 2009;174:1149–53.
    OpenUrlCrossRefPubMed
  11. 11.↵
    1. Ichimura K,
    2. Pearson DM,
    3. Kocialkowski S,
    4. Backlund LM,
    5. Chan R,
    6. Jones DT,
    7. et al.
    IDH1 mutations are present in the majority of common adult gliomas but rare in primary glioblastomas. Neuro Oncol 2009;11:341–7.
    OpenUrlAbstract/FREE Full Text
  12. 12.↵
    1. Balss J,
    2. Meyer J,
    3. Mueller W,
    4. Korshunov A,
    5. Hartmann C,
    6. von Deimling A
    . Analysis of the IDH1 codon 132 mutation in brain tumors. Acta Neuropathol 2008;116:597–602.
    OpenUrlCrossRefPubMed
  13. 13.↵
    1. Nobusawa S,
    2. Watanabe T,
    3. Kleihues P,
    4. Ohgaki H
    . IDH1 mutations as molecular signature and predictive factor of secondary glioblastomas. Clin Cancer Res 2009;15:6002–7.
    OpenUrlAbstract/FREE Full Text
  14. 14.↵
    1. Vogelstein B,
    2. Kinzler KW
    . The multistep nature of cancer. Trends Genet 1993;9:138–41.
    OpenUrlCrossRefPubMed
  15. 15.↵
    1. Johnson BE,
    2. Mazor T,
    3. Hong C,
    4. Barnes M,
    5. Aihara K,
    6. McLean CY,
    7. et al.
    Mutational analysis reveals the origin and therapy-driven evolution of recurrent glioma. Science 2014;343:189–93.
    OpenUrlAbstract/FREE Full Text
  16. 16.↵
    1. Turcan S,
    2. Rohle D,
    3. Goenka A,
    4. Walsh LA,
    5. Fang F,
    6. Yilmaz E,
    7. et al.
    IDH1 mutation is sufficient to establish the glioma hypermethylator phenotype. Nature 2012;483:479–83.
    OpenUrlCrossRefPubMed
  17. 17.↵
    1. Kannan K,
    2. Inagaki A,
    3. Silber J,
    4. Gorovets D,
    5. Zhang J,
    6. Kastenhuber ER,
    7. et al.
    Whole-exome sequencing identifies ATRX mutation as a key molecular determinant in lower-grade glioma. Oncotarget 2012;3:1194–203.
    OpenUrlPubMed
  18. 18.↵
    1. Yan H,
    2. Bigner DD,
    3. Velculescu V,
    4. Parsons DW
    . Mutant metabolic enzymes are at the origin of gliomas. Cancer Res 2009;69:9157–9.
    OpenUrlAbstract/FREE Full Text
  19. 19.↵
    1. Gerlinger M,
    2. Rowan AJ,
    3. Horswell S,
    4. Larkin J,
    5. Endesfelder D,
    6. Gronroos E,
    7. et al.
    Intratumor heterogeneity and branched evolution revealed by multiregion sequencing. N Engl J Med 2012;366:883–92.
    OpenUrlCrossRefPubMed
  20. 20.↵
    1. Capper D,
    2. Weissert S,
    3. Balss J,
    4. Habel A,
    5. Meyer J,
    6. Jager D,
    7. et al.
    Characterization of R132H mutation-specific IDH1 antibody binding in brain tumors. Brain Pathol 2010;20:245–54.
    OpenUrlCrossRefPubMed
  21. 21.↵
    1. Walker EJ,
    2. Zhang C,
    3. Castelo-Branco P,
    4. Hawkins C,
    5. Wilson W,
    6. Zhukova N,
    7. et al.
    Monoallelic expression determines oncogenic progression and outcome in benign and malignant brain tumors. Cancer Res 2012;72:636–44.
    OpenUrlAbstract/FREE Full Text
  22. 22.↵
    1. Klink B,
    2. Miletic H,
    3. Stieber D,
    4. Huszthy PC,
    5. Valenzuela JA,
    6. Balss J,
    7. et al.
    A novel, diffusely infiltrative xenograft model of human anaplastic oligodendroglioma with mutations in FUBP1, CIC, and IDH1. PLoS ONE 2013;8:e59773.
    OpenUrlCrossRefPubMed
  23. 23.↵
    1. Joo KM,
    2. Kim J,
    3. Jin J,
    4. Kim M,
    5. Seol HJ,
    6. Muradov J,
    7. et al.
    Patient-specific orthotopic glioblastoma xenograft models recapitulate the histopathology and biology of human glioblastomas in situ . Cell Rep 2013;3:260–73.
    OpenUrlCrossRefPubMed
  24. 24.↵
    1. Luchman HA,
    2. Stechishin OD,
    3. Dang NH,
    4. Blough MD,
    5. Chesnelong C,
    6. Kelly JJ,
    7. et al.
    An in vivo patient-derived model of endogenous IDH1-mutant glioma. Neuro Oncol 2012;14:184–91.
    OpenUrlAbstract/FREE Full Text
  25. 25.↵
    1. Kelly JJ,
    2. Blough MD,
    3. Stechishin OD,
    4. Chan JA,
    5. Beauchamp D,
    6. Perizzolo M,
    7. et al.
    Oligodendroglioma cell lines containing t(1;19)(q10;p10). Neuro Oncol 2010;12:745–55.
    OpenUrlAbstract/FREE Full Text
  26. 26.↵
    1. Broderick DK,
    2. Di C,
    3. Parrett TJ,
    4. Samuels YR,
    5. Cummins JM,
    6. McLendon RE,
    7. et al.
    Mutations of PIK3CA in anaplastic oligodendrogliomas, high-grade astrocytomas, and medulloblastomas. Cancer Res 2004;64:5048–50.
    OpenUrlAbstract/FREE Full Text
  27. 27.↵
    1. Phillips JJ,
    2. Aranda D,
    3. Ellison DW,
    4. Judkins AR,
    5. Croul SE,
    6. Brat DJ,
    7. et al.
    PDGFRA amplification is common in pediatric and adult high-grade astrocytomas and identifies a poor prognostic group in IDH1 mutant glioblastoma. Brain Pathol 2013;23:565–73.
    OpenUrlCrossRefPubMed
  28. 28.↵
    1. Wen PY,
    2. Macdonald DR,
    3. Reardon DA,
    4. Cloughesy TF,
    5. Sorensen AG,
    6. Galanis E,
    7. et al.
    Updated response assessment criteria for high-grade gliomas: response assessment in neuro-oncology working group. J Clin Oncol 2010;28:1963–72.
    OpenUrlAbstract/FREE Full Text
  29. 29.↵
    1. Wakimoto H,
    2. Kesari S,
    3. Farrell C,
    4. Curry WJ,
    5. Zaupa C,
    6. Aghi M,
    7. et al.
    Human glioblastoma-derived cancer stem cells: establishment of invasive glioma models and treatment with oncolytic herpes simplex virus vectors. Cancer Res 2009;69:3472–81.
    OpenUrlAbstract/FREE Full Text
  30. 30.↵
    1. Yuan X,
    2. Curtin J,
    3. Xiong Y,
    4. Liu G,
    5. Waschsmann-Hogiu S,
    6. Farkas D,
    7. et al.
    Isolation of cancer stem cells from adult glioblastoma multiforme. Oncogene 2004;23:9392–400.
    OpenUrlCrossRefPubMed
  31. 31.↵
    1. Wakimoto H,
    2. Mohapatra G,
    3. Kanai R,
    4. Curry WT Jr..,
    5. Yip S,
    6. Nitta M,
    7. et al.
    Maintenance of primary tumor phenotype and genotype in glioblastoma stem cells. Neuro Oncol 2012;14:132–44.
    OpenUrlAbstract/FREE Full Text
  32. 32.↵
    1. Chi AS,
    2. Batchelor TT,
    3. Dias-Santagata D,
    4. Borger D,
    5. Stiles CD,
    6. Wang DL,
    7. et al.
    Prospective, high-throughput molecular profiling of human gliomas. J Neurooncol 2012;110:89–98.
    OpenUrlCrossRefPubMed
  33. 33.↵
    1. Dias-Santagata D,
    2. Akhavanfard S,
    3. David SS,
    4. Vernovsky K,
    5. Kuhlmann G,
    6. Boisvert SL,
    7. et al.
    Rapid targeted mutational analysis of human tumours: a clinical platform to guide personalized cancer medicine. EMBO Mol Med 2010;2:146–58.
    OpenUrlAbstract/FREE Full Text
  34. 34.↵
    1. Fendt SM,
    2. Bell EL,
    3. Keibler MA,
    4. Olenchock BA,
    5. Mayers JR,
    6. Wasylenko TM,
    7. et al.
    Reductive glutamine metabolism is a function of the α-ketoglutarate to citrate ratio in cells. Nat Commun 2013;4:2236.
    OpenUrlPubMed
  35. 35.↵
    1. Fendt SM,
    2. Bell EL,
    3. Keibler MA,
    4. Davidson SM,
    5. Wirth GJ,
    6. Fiske B,
    7. et al.
    Metformin decreases glucose oxidation and increases the dependency of prostate cancer cells on reductive glutamine metabolism. Cancer Res 2013;73:4429–38.
    OpenUrlAbstract/FREE Full Text
  36. 36.↵
    1. Hartmann C,
    2. Meyer J,
    3. Balss J,
    4. Capper D,
    5. Mueller W,
    6. Christians A,
    7. et al.
    Type and frequency of IDH1 and IDH2 mutations are related to astrocytic and oligodendroglial differentiation and age: a study of 1,010 diffuse gliomas. Acta Neuropathol 2009;118:469–74.
    OpenUrlCrossRefPubMed
  37. 37.↵
    1. Jin G,
    2. Reitman ZJ,
    3. Duncan CG,
    4. Spasojevic I,
    5. Gooden DM,
    6. Rasheed BA,
    7. et al.
    Disruption of wild-type IDH1 suppresses D-2-hydroxyglutarate production in IDH1-mutated gliomas. Cancer Res 2013;73:496–501.
    OpenUrlAbstract/FREE Full Text
  38. 38.↵
    1. Perry A,
    2. Miller CR,
    3. Gujrati M,
    4. Scheithauer BW,
    5. Zambrano SC,
    6. Jost SC,
    7. et al.
    Malignant gliomas with primitive neuroectodermal tumor-like components: a clinicopathologic and genetic study of 53 cases. Brain Pathol 2009;19:81–90.
    OpenUrlCrossRefPubMed
  39. 39.↵
    1. Furet P,
    2. Guagnano V,
    3. Fairhurst RA,
    4. Imbach-Weese P,
    5. Bruce I,
    6. Knapp M,
    7. et al.
    Discovery of NVP-BYL719 a potent and selective phosphatidylinositol-3 kinase alpha inhibitor selected for clinical evaluation. Bioorg Med Chem Lett 2013;23:3741–8.
    OpenUrlCrossRefPubMed
  40. 40.↵
    1. Delmore JE,
    2. Issa GC,
    3. Lemieux ME,
    4. Rahl PB,
    5. Shi J,
    6. Jacobs HM,
    7. et al.
    BET bromodomain inhibition as a therapeutic strategy to target c-Myc. Cell 2011;146:904–17.
    OpenUrlCrossRefPubMed
  41. 41.↵
    1. Burford A,
    2. Little SE,
    3. Jury A,
    4. Popov S,
    5. Laxton R,
    6. Doey L,
    7. et al.
    Distinct phenotypic differences associated with differential amplification of receptor tyrosine kinase genes at 4q12 in glioblastoma. PLoS ONE 2013;8:e71777.
    OpenUrlCrossRefPubMed
  42. 42.↵
    1. Odia Y,
    2. Orr BA,
    3. Robert Bell W,
    4. Eberhart CG,
    5. Rodriguez FJ
    . cMYC expression in infiltrating gliomas: associations with IDH1 mutations, clinicopathologic features and outcome. J Neurooncol 2013;115:249–59.
    OpenUrlCrossRefPubMed
  43. 43.↵
    1. Chen C,
    2. Liu Y,
    3. Lu C,
    4. Cross JR,
    5. Morris JPt,
    6. Shroff AS,
    7. et al.
    Cancer-associated IDH2 mutants drive an acute myeloid leukemia that is susceptible to Brd4 inhibition. Genes Dev 2013;27:1974–85.
    OpenUrlAbstract/FREE Full Text
  44. 44.↵
    1. Hunter C,
    2. Smith R,
    3. Cahill D,
    4. Stephens P,
    5. Stevens C,
    6. Teague J,
    7. et al.
    A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapy. Cancer Res 2006;66:3987–91.
    OpenUrlAbstract/FREE Full Text
  45. 45.↵
    Cancer Genome Atlas Research Network. Comprehensive genomic characterization defines human glioblastoma genes and core pathways. Nature 2008;455:1061–8.
    OpenUrlCrossRefPubMed
  46. 46.↵
    1. van den Bent MJ,
    2. Brandes AA,
    3. Taphoorn MJ,
    4. Kros JM,
    5. Kouwenhoven MC,
    6. Delattre JY,
    7. et al.
    Adjuvant procarbazine, lomustine, and vincristine chemotherapy in newly diagnosed anaplastic oligodendroglioma: long-term follow-up of EORTC brain tumor group study 26951. J Clin Oncol 2013;31:344–50.
    OpenUrlAbstract/FREE Full Text
  47. 47.↵
    1. Cairncross G,
    2. Wang M,
    3. Shaw E,
    4. Jenkins R,
    5. Brachman D,
    6. Buckner J,
    7. et al.
    Phase III trial of chemoradiotherapy for anaplastic oligodendroglioma: long-term results of RTOG 9402. J Clin Oncol 2013;31:337–43.
    OpenUrlAbstract/FREE Full Text
  48. 48.↵
    1. Knobbe CB,
    2. Reifenberger J,
    3. Reifenberger G
    . Mutation analysis of the Ras pathway genes NRAS, HRAS, KRAS and BRAF in glioblastomas. Acta Neuropathol 2004;108:467–70.
    OpenUrlCrossRefPubMed
  49. 49.↵
    1. Jeuken J,
    2. van den Broecke C,
    3. Gijsen S,
    4. Boots-Sprenger S,
    5. Wesseling P
    . RAS/RAF pathway activation in gliomas: the result of copy number gains rather than activating mutations. Acta Neuropathol 2007;114:121–33.
    OpenUrlCrossRefPubMed
  50. 50.↵
    1. Janne PA,
    2. Shaw AT,
    3. Pereira JR,
    4. Jeannin G,
    5. Vansteenkiste J,
    6. Barrios C,
    7. et al.
    Selumetinib plus docetaxel for KRAS-mutant advanced non-small-cell lung cancer: a randomised, multicentre, placebo-controlled, phase 2 study. Lancet Oncol 2013;14:38–47.
    OpenUrlCrossRefPubMed
View Abstract
PreviousNext
Back to top
Clinical Cancer Research: 20 (11)
June 2014
Volume 20, Issue 11
  • Table of Contents
  • Table of Contents (PDF)
  • About the Cover

Sign up for alerts

View this article with LENS

Open full page PDF
Article Alerts
Sign In to Email Alerts with your Email Address
Email Article

Thank you for sharing this Clinical Cancer Research article.

NOTE: We request your email address only to inform the recipient that it was you who recommended this article, and that it is not junk mail. We do not retain these email addresses.

Enter multiple addresses on separate lines or separate them with commas.
Targetable Signaling Pathway Mutations Are Associated with Malignant Phenotype in IDH-Mutant Gliomas
(Your Name) has forwarded a page to you from Clinical Cancer Research
(Your Name) thought you would be interested in this article in Clinical Cancer Research.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Citation Tools
Targetable Signaling Pathway Mutations Are Associated with Malignant Phenotype in IDH-Mutant Gliomas
Hiroaki Wakimoto, Shota Tanaka, William T. Curry, Franziska Loebel, Dan Zhao, Kensuke Tateishi, Juxiang Chen, Lindsay K. Klofas, Nina Lelic, James C. Kim, Dora Dias-Santagata, Leif W. Ellisen, Darrell R. Borger, Sarah-Maria Fendt, Matthew G. Vander Heiden, Tracy T. Batchelor, A. John Iafrate, Daniel P. Cahill and Andrew S. Chi
Clin Cancer Res June 1 2014 (20) (11) 2898-2909; DOI: 10.1158/1078-0432.CCR-13-3052

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Share
Targetable Signaling Pathway Mutations Are Associated with Malignant Phenotype in IDH-Mutant Gliomas
Hiroaki Wakimoto, Shota Tanaka, William T. Curry, Franziska Loebel, Dan Zhao, Kensuke Tateishi, Juxiang Chen, Lindsay K. Klofas, Nina Lelic, James C. Kim, Dora Dias-Santagata, Leif W. Ellisen, Darrell R. Borger, Sarah-Maria Fendt, Matthew G. Vander Heiden, Tracy T. Batchelor, A. John Iafrate, Daniel P. Cahill and Andrew S. Chi
Clin Cancer Res June 1 2014 (20) (11) 2898-2909; DOI: 10.1158/1078-0432.CCR-13-3052
del.icio.us logo Digg logo Reddit logo Twitter logo CiteULike logo Facebook logo Google logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Jump to section

  • Article
    • Abstract
    • Introduction
    • Materials and Methods
    • Results
    • Discussion
    • Disclosure of Potential Conflicts of Interest
    • Authors' Contributions
    • Grant Support
    • Acknowledgments
    • Footnotes
    • References
  • Figures & Data
  • Info & Metrics
  • PDF
Advertisement

Related Articles

Cited By...

More in this TOC Section

  • Sirt7 Promotes Colorectal Cancer Tumorigenesis
  • Contact Guidance Controls T-cell Migration in PDAC
  • MET in Papillary RCC
Show more Human Cancer Biology
  • Home
  • Alerts
  • Feedback
  • Privacy Policy
Facebook  Twitter  LinkedIn  YouTube  RSS

Articles

  • Online First
  • Current Issue
  • Past Issues
  • CCR Focus Archive
  • Meeting Abstracts

Info for

  • Authors
  • Subscribers
  • Advertisers
  • Librarians

About Clinical Cancer Research

  • About the Journal
  • Editorial Board
  • Permissions
  • Submit a Manuscript
AACR logo

Copyright © 2021 by the American Association for Cancer Research.

Clinical Cancer Research
eISSN: 1557-3265
ISSN: 1078-0432

Advertisement