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

  • 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
      • Clinical Trials
      • Immunotherapy: Facts and Hopes
      • Editors' Picks
  • For Authors
    • Information for Authors
    • Author Services
    • Best of: Author Profiles
    • Submit
  • Alerts
    • Table of Contents
    • OnlineFirst
    • Editors' Picks
    • Citation
    • Author/Keyword
  • News
    • Cancer Discovery News
  • 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

Advanced Search

  • Home
  • About
    • The Journal
    • AACR Journals
    • Subscriptions
    • Permissions and Reprints
    • Reviewing
    • CME
  • Articles
    • OnlineFirst
    • Current Issue
    • Past Issues
    • CCR Focus Archive
    • Meeting Abstracts
    • Collections
      • Clinical Trials
      • Immunotherapy: Facts and Hopes
      • Editors' Picks
  • For Authors
    • Information for Authors
    • Author Services
    • Best of: Author Profiles
    • Submit
  • Alerts
    • Table of Contents
    • OnlineFirst
    • Editors' Picks
    • Citation
    • Author/Keyword
  • News
    • Cancer Discovery News
Regular Articles

The Expression of PAX6, PTEN, Vascular Endothelial Growth Factor, and Epidermal Growth Factor Receptor in Gliomas

Relationship to Tumor Grade and Survival

Yi-Hong Zhou, Fang Tan, Kenneth R. Hess and W. K. Alfred Yung
Yi-Hong Zhou
Departments of Neuro-Oncology [Y-H. Z., F. T., W. K. A. Y.] and Biostatistics [K. R. H.], The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Fang Tan
Departments of Neuro-Oncology [Y-H. Z., F. T., W. K. A. Y.] and Biostatistics [K. R. H.], The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Kenneth R. Hess
Departments of Neuro-Oncology [Y-H. Z., F. T., W. K. A. Y.] and Biostatistics [K. R. H.], The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
W. K. Alfred Yung
Departments of Neuro-Oncology [Y-H. Z., F. T., W. K. A. Y.] and Biostatistics [K. R. H.], The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
DOI:  Published August 2003
  • Article
  • Figures & Data
  • Info & Metrics
  • PDF
Loading

Article Figures & Data

Figures

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

    PAX6 expression in glioma cell lines and chromosome 10 hybrid clones measured by real-time quantitative RT-PCR. A, relative expression level of PAX6 gene normalized by enolase-α (▪) or GAPDH (□), and the value of 1 was assigned for U251. N10.5.6, N10.6, and N10.8 are U251-chromosomal 10 hybrid clones. NHA is a normal astrocytic cell line. The tumorigenicity of each cell line in nu/nu mice (LT, low tumorigenic) is from Ke et al. (14) and Ishii et al. (28) . B, comparison of relative PAX6 expression level in glioma cells grouped into none- and low- (NT/LT) tumorigenic and HT cells. The P was from a two-sample unequal variance t test. The position of a bar and a vertical line for each class indicates the mean and SD, respectively.

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

    Analysis of the relative levels of PAX6, PTEN, VEGF, and EGFR gene expression by real-time quantitative RT-PCR in 45 AA, 42 GBM, and 7 samples of adjacent normal tissue, and normalized by β-actin. The Y axis is a log 10-transformed PAX6:β-actin ratio. The position of a bar and a vertical line for each class indicate the mean and SD, respectively. The statistical significance between AAs and GBMs is shown by Ps.

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

    Kaplan-Meier survival curves for 86 patients with astrocytic malignant gliomas above and below the cutpoint of the β-actin normalized PAX6 gene expression value derived from optimal dichotomization.

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

    Kaplan-Meier survival curves for the same set of patients as in Fig. 3<$REFLINK> based on β-actin normalized expression values of PAX6 and PTEN genes derived from recursive partitioning analysis.

Tables

  • Figures
  • Table 1

    Median expression levels normalized by β-actin

    GenesNormal (n = 7)AA (n = 45)GBM (n = 42)
    PAX6 0.0180.0190.006
    PTEN 0.0120.0100.004
    EGFR 0.0070.0130.027
    VEGF 0.0290.0210.086
  • Table 2

    Comparison of relative PAX6 expression levels in the same patients

    Patient #TissuePAX6/β-actinNormal/tumor (AA/GBM)
    1Normal0.07111.2
    GBM0.006
    2Normal0.0279.0
    GBM0.003
    3Normal0.0121.9
    GBM0.006
    4Normal0.0104.0
    GBM0.003
    5Normal0.0132.5
    GBM0.005
    6Normal0.0811.9
    AA0.042
    7Normal0.0181.0
    AA0.019
    8AA0.03231.1
    GBM0.001
  • Table 3

    P from Cox proportional hazards regression analyses using dichotomized cutpoints

    GeneUnivariatea4 variatesb7 variatesc
    PAX60.00020.00740.0006
    PTEN<0.00010.00110.0002
    VEGF<0.00010.00650.0006
    EGFR0.0210.120.80
    • a Each gene analyzed individually.

    • b Same as for a, but also adjusting for age, histology, and recurrence status.

    • c All four genes included in a single model with age, histology, and recurrence status.

  • Table 4

    Proportion of variation in survival explained by the models

    ModelClinical variatesClinical variates + each gene7 variates
    PAX6PTENVEGFEGFR
    Proportion30%36%39%37%32%55%
PreviousNext
Back to top
Clinical Cancer Research: 9 (9)
August 2003
Volume 9, Issue 9
  • Table of Contents
  • 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.
The Expression of PAX6, PTEN, Vascular Endothelial Growth Factor, and Epidermal Growth Factor Receptor in 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.
Citation Tools
The Expression of PAX6, PTEN, Vascular Endothelial Growth Factor, and Epidermal Growth Factor Receptor in Gliomas
Yi-Hong Zhou, Fang Tan, Kenneth R. Hess and W. K. Alfred Yung
Clin Cancer Res August 15 2003 (9) (9) 3369-3375;

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Share
The Expression of PAX6, PTEN, Vascular Endothelial Growth Factor, and Epidermal Growth Factor Receptor in Gliomas
Yi-Hong Zhou, Fang Tan, Kenneth R. Hess and W. K. Alfred Yung
Clin Cancer Res August 15 2003 (9) (9) 3369-3375;
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

Regular Articles

  • Intermittent Hypoxia Induces Proteasome-Dependent Down-Regulation of Estrogen Receptor α in Human Breast Carcinoma
  • Potent and Specific Antitumor Efficacy of CMC-544, a CD22-Targeted Immunoconjugate of Calicheamicin, against Systemically Disseminated B-Cell Lymphoma
  • Ring Finger Protein 43 as a New Target for Cancer Immunotherapy
Show more Regular Articles

Molecular Oncology, Markers, Clinical Correlates

  • Prognostic Impact of Hypoxia-Inducible Factors 1α and 2α in Colorectal Cancer Patients
  • Impact of Vascular Endothelial Growth Factor-C and -D Expression in Human Pancreatic Cancer
  • mTOR and P70 S6 Kinase Expression in Primary Liver Neoplasms
Show more Molecular Oncology, Markers, Clinical Correlates
  • 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
  • Reviewers

About Clinical Cancer Research

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

Copyright © 2019 by the American Association for Cancer Research.

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

Advertisement