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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
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Kirk J. Wojno
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Michael T. McCabe
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Rainer Kuefer
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Juergen E. Gschwend
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Mark L. Day
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DOI: 10.1158/1078-0432.CCR-06-2381 Published April 2007
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Abstract

Purpose: We have previously shown that 5-aza-2′-deoxycytidine (5-aza) is an effective chemopreventive agent capable of preventing early disease progression in the transgenic adenocarcinoma of the mouse prostate (TRAMP) model. The purpose of this study was to determine the effect of 5-aza on preexisting TRAMP prostate cancers and prevention of androgen-independent prostate cancer.

Experimental Design: TRAMP mice with established prostate cancers were treated with 5-aza, castration, castration + 5-aza, or vehicle control (PBS). One cohort of 22 mice per treatment was euthanized after 10 weeks of treatment, whereas a second cohort of 14 mice per group was followed until death to determine survival. Histologic sections of prostate, pelvic lymph nodes, lung, and liver were blinded and analyzed by a certified genitourinary pathologist (K.J.W.).

Results: Combined treatment (castration + 5-aza) provided significant survival benefits over either single treatment (combined versus castration P = 0.029, combined versus 5-aza P = 0.036). At 24 weeks of age, 86% of mice within the PBS cohort exhibited histologic evidence of prostate cancer, whereas only 47% of the combined cohort exhibited malignant disease (P < 0.0001). Additionally, whereas 43% of the PBS treatment group exhibited lymph node metastases, these were only observed in 21% of the combined treatment mice.

Conclusions: This is the first study to examine the effect of 5-aza and combined castration + 5-aza on preexisting prostate cancer in an animal model. Based on these preclinical findings, we suggest that 5-aza treatment may prolong the time to an androgen-independent status and thus survival in a hormone-deprived setting in prostate cancer.

  • 5-aza
  • castration
  • prostate cancer
  • androgen-independence
  • TRAMP

Footnotes

  • Grant support: University of Michigan Specialized Program of Research Excellence for Prostate Cancer National Cancer Institute grant P50CA69569 and NIH National Institutes of Diabetes, Digestive and Kidney Diseases grant DK61488 (M.L. Day).

  • 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.

    • Accepted January 9, 2007.
    • Received September 28, 2006.
    • Revision received December 18, 2006.
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Clinical Cancer Research: 13 (7)
April 2007
Volume 13, Issue 7
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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

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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
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Clinical Cancer Research
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