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

Cancer Therapy: Preclinical

5-Aza-2′-Deoxycytidine Delays Androgen-Independent Disease and Improves Survival in the Transgenic Adenocarcinoma of the Mouse Prostate Mouse Model of Prostate Cancer

Christoph S. Zorn, Kirk J. Wojno, Michael T. McCabe, Rainer Kuefer, Juergen E. Gschwend and Mark L. Day
Christoph S. Zorn
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Kirk J. Wojno
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Michael T. McCabe
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Rainer Kuefer
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Juergen E. Gschwend
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Mark L. Day
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
DOI: 10.1158/1078-0432.CCR-06-2381 Published April 2007
  • 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 schedule. Treatment for all treatment groups was started at 15 wk of age. Vehicle control (PBS) or 5-aza injections were administered thrice a week for 10 wk for all groups. Mice were either euthanized at 24 wk or allowed to survive until death. For every TRAMP treatment group, there was a wild-type (WT) control group.

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

    Weight of the prostate (dorsal, lateral, and ventral lobe) at 24 wk and survival. *, P = 0.017 using the Mann-Whitney test between 5-aza survival and PBS survival. Bar, median for each group.

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

    Representative H&E staining of TRAMP tumors from all treatment groups at 24 wk. A, poorly differentiated adenocarcinoma of the prostate from a PBS-treated animal (×20). B, prostatic intraepithelial neoplasia in a 5-aza–treated animal (×60). C, normal prostate from a combined treatment mouse (×60). D, poorly differentiated adenocarcinoma from the castration group (×20). Bar, 100 μm. E and F, metastatic deposits of prostate cancer in the brain.

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

    Treatment with castration + 5-aza significantly increases survival of TRAMP mice. Treatment duration is indicated. A, Kaplan-Meier analysis for PBS and combined treatment. B, Kaplan-Meier analysis for castration and combined treatment. C, Kaplan-Meier analysis for 5-aza and combined treatment. D, Kaplan-Meier analysis of all treatment groups.

Tables

  • Figures
  • Table 1.

    Effect of treatments on histologic distribution of lesions in TRAMP mice at 24 wks

    Treatment groupnHistology
    PLN Mets (%)P
    NormalPINWDMDPD
    Castration + 5-aza19585003721
    PBS2101414567<0.0001*430.19†
    5-Aza22144150410.007‡180.10§
    Castration1930000700.19∥370.29¶
    • Abbreviations: PIN, prostatic intraepithelial neoplasia; WD, well-differentiated prostate cancer; MD, moderately differentiated prostate cancer; PD, poorly-differentiated prostate cancer; LN, lymph node; Mets, metastasis.

    • ↵* Fisher's exact test comparing the frequency of normal pathology between castration + 5-aza and PBS groups.

    • ↵† Fisher's exact test comparing the frequency of lymph node metastasis between castration + 5-aza and PBS groups.

    • ↵‡ Fisher's exact test comparing the frequency of normal pathology between castration + 5-aza and 5-aza groups.

    • ↵§ Fisher's exact test comparing the frequency of lymph node metastasis between 5-aza and PBS groups.

    • ↵∥ Fisher's exact test comparing the frequency of normal pathology between castration + 5-aza and castration groups.

    • ↵¶ Fisher's exact test comparing the frequency of lymph node metastasis between castration and 5-aza groups.

PreviousNext
Back to top
Clinical Cancer Research: 13 (7)
April 2007
Volume 13, Issue 7
  • 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.
5-Aza-2′-Deoxycytidine Delays Androgen-Independent Disease and Improves Survival in the Transgenic Adenocarcinoma of the Mouse Prostate Mouse Model of Prostate Cancer
(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
5-Aza-2′-Deoxycytidine Delays Androgen-Independent Disease and Improves Survival in the Transgenic Adenocarcinoma of the Mouse Prostate Mouse Model of Prostate Cancer
Christoph S. Zorn, Kirk J. Wojno, Michael T. McCabe, Rainer Kuefer, Juergen E. Gschwend and Mark L. Day
Clin Cancer Res April 1 2007 (13) (7) 2136-2143; DOI: 10.1158/1078-0432.CCR-06-2381

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Share
5-Aza-2′-Deoxycytidine Delays Androgen-Independent Disease and Improves Survival in the Transgenic Adenocarcinoma of the Mouse Prostate Mouse Model of Prostate Cancer
Christoph S. Zorn, Kirk J. Wojno, Michael T. McCabe, Rainer Kuefer, Juergen E. Gschwend and Mark L. Day
Clin Cancer Res April 1 2007 (13) (7) 2136-2143; DOI: 10.1158/1078-0432.CCR-06-2381
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
    • Materials and Methods
    • Results and Discussion
    • Acknowledgments
    • Footnotes
    • References
  • Figures & Data
  • Info & Metrics
  • PDF
Advertisement

Related Articles

Cited By...

More in this TOC Section

  • PK/PD Model of a Bispecific DART Molecule in Monkeys
  • STAT3/HOTAIR/EZH2 Regulates HNSCC Growth
  • TAZ is a Potent Mediator of aRMS Tumorigenesis
Show more Cancer Therapy: Preclinical
  • 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