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
  • 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
  • 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

Experimental Therapeutics, Preclinical Pharmacology

Antitumor Activity of CEP-751 (KT-6587) on Human Neuroblastoma and Medulloblastoma Xenografts

Audrey E. Evans, Kristin D. Kisselbach, Darrell J. Yamashiro, Naohiko Ikegaki, Anna Marie Camoratto, Craig A. Dionne and Garrett M. Brodeur
Audrey E. Evans
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Kristin D. Kisselbach
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Darrell J. Yamashiro
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Naohiko Ikegaki
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Anna Marie Camoratto
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Craig A. Dionne
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Garrett M. Brodeur
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
DOI:  Published November 1999
  • Article
  • Figures & Data
  • Info & Metrics
  • PDF
Loading

Article Figures & Data

Figures

  • Tables
  • Fig. 1.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 1.

    Treatment effect of CEP-751 on NBL cell lines grown in nude mice. A, IMR-5; B, CHP-134; C, NBL-S therapeutic studies; D, IMR-5 prevention study results; E and F, CHP-134 prevention study comparing the treatment effect of six early- and six late-appearing tumors (see Table 1<$REFLINK> ). Bars, SE.

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

    Treatment effect of CEP-751 on 2 MBL cell lines grown in nude mice. Therapeutic studies: A, D341; B, D283. Prevention study: C, D341. Bars, SE. (See Table 2<$REFLINK> .)

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

    Treatment effect of CEP-751 on SY5Y NBL cells (A) and two TrkB transfected clones, SY5Y-G8 (B) and SY5Y-G12 (C).

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

    Effect of compound on apoptosis in CHP134 tumors obtained after 1, 3, and 5 days of treatment. Left (from top to bottom), DAPI stained tumor cells on days 2, 4, and 6. Right (from top to bottom), TUNEL stained tumor cells on days 2, 4, and 6. The second and third rows show progressive increase in apoptotic cells with time, as detected by the TUNEL assay, in CEP-751 treated tumors.

Tables

  • Figures
  • Table 1

    In vivo studies of NBL

    Tumor size (cm3)Analysis of slopea
    Cell lineDay of analysisCompoundControlCompoundControl
    A. Neuroblastoma therapeutic studiesb
    IMR-5121.96 ± 0.35 (n = 5)3.91 ± 1.22 (n = 5)0.17 ± 0.051 (n = 5)0.28 ± 0.109 (n = 5)
    P = 0.025P = 0.024
    CHP 134151.9 ± 0.75 (n = 4)4.5 ± 0.98 (n = 3)0.151 ± 0.055 (n = 6)0.299 ± 0.068 (n = 5)
    P = 0.034P = 0.12
    NBL-S170.94 ± 0.24 (n = 5)5.2 ± 2.46 (n = 4)0.15 ± 0.034 (n = 5)0.264 ± 0.014 (n = 4)
    P = 0.016P = 0.12
    B. Neuroblastoma prevention studiesc
    IMR-5271.3 ± 1.63 (n = 7)2.7 ± 1.55 (n = 6)0.118 ± 0.036 (n = 7)0.188 ± 0.041 (n = 6)
    P = 0.062P = 0.073
    CHP 134 (combined)See text0.064 ± (n = 6)0.122 ± (n = 6)
    P = 0.058
    CHP 134 (early)29See text0.148 ± 0.013 (n = 3)0.169 ± 0.01 (n = 3)
    P = 0.28
    CHP 134 (late)58See text0.022 ± 0.011 (n = 3)0.140 ± 0.009 (n = 3)
    P = 0.049
    • a Figures given for the average daily growth rate.

    • b Treatment started after tumors measured >0.24 g.

    • c Treatment commenced prior to tumor appearance.

  • Table 2

    In vivo studies of MBL

    Tumor size (cm3)Analysis of slopea
    Cell lineDay of analysisCompoundControlCompoundControl
    A. Medulloblastoma therapeutic studiesb
    D341151.98 ± 1.86 (n = 5)2.24 ± 0.790 (n = 5)0.199 ± 0.091 (n = 6)0.238 ± 0.068 (n = 6)
    P = 0.60P = 0.75
    DAOY161.51 ± 0.689 (n = 5)1.97 ± 0.603 (n = 3)0.152 ± 0.045 (n = 5)0.151 ± 0.069 (n = 3)
    P = 0.39P = 0.96
    D283391.044 ± 0.297 (n = 8)1.54 ± 0.51 (n = 8)0.017 ± 0.008 (n = 8)0.031 ± 0.012 (n = 8)
    P = 0.031P = 0.021
    B. Medulloblastoma prevention studyc
    D341160.91 ± 0.92 (n = 5)2.17 ± 1.42 (n = 6)0.092 ± 0.072 (n = 8)0.186 ± 0.039 (n = 9)
    P = 0.10P = 0.126
    • a Figures given for the average daily growth rate.

    • b Treatment started after tumors measured >0.24 g.

    • c Treatment commenced prior to tumor appearance.

PreviousNext
Back to top
November 1999
Volume 5, Issue 11
  • Table of Contents

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.
Antitumor Activity of CEP-751 (KT-6587) on Human Neuroblastoma and Medulloblastoma Xenografts
(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
Antitumor Activity of CEP-751 (KT-6587) on Human Neuroblastoma and Medulloblastoma Xenografts
Audrey E. Evans, Kristin D. Kisselbach, Darrell J. Yamashiro, Naohiko Ikegaki, Anna Marie Camoratto, Craig A. Dionne and Garrett M. Brodeur
Clin Cancer Res November 1 1999 (5) (11) 3594-3602;

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Share
Antitumor Activity of CEP-751 (KT-6587) on Human Neuroblastoma and Medulloblastoma Xenografts
Audrey E. Evans, Kristin D. Kisselbach, Darrell J. Yamashiro, Naohiko Ikegaki, Anna Marie Camoratto, Craig A. Dionne and Garrett M. Brodeur
Clin Cancer Res November 1 1999 (5) (11) 3594-3602;
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
    • Acknowledgments
    • Footnotes
    • References
  • Figures & Data
  • Info & Metrics
  • PDF
Advertisement

Related Articles

Cited By...

More in this TOC Section

  • Potent and Specific Antitumor Efficacy of CMC-544, a CD22-Targeted Immunoconjugate of Calicheamicin, against Systemically Disseminated B-Cell Lymphoma
  • Intermittent Hypoxia Induces Proteasome-Dependent Down-Regulation of Estrogen Receptor α in Human Breast Carcinoma
  • Mouse Homologue of a Novel Human Oncofetal Antigen, Glypican-3, Evokes T-Cell–Mediated Tumor Rejection without Autoimmune Reactions in Mice
Show more Experimental Therapeutics, Preclinical Pharmacology
  • 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