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Gene silencing in androgen-responsive prostate cancer cells from the tissue-specific prostate-specific antigen promoter.

Song J, Pang S, Lu Y, Yokoyama KK, Zheng JY, Chiu R

Dental Research Institute, University of California Los Angeles (UCLA) School of Dentistry, UCLA, Los Angeles, California 90095, USA.

The success of gene therapy using a RNA interference approach relies on small interfering RNA (siRNA) expression from a highly tissue-specific RNA polymerase II promoter rather than from ubiquitous RNA polymerase III. Accordingly, we have developed a prostate-specific vector that expresses siRNAs from the human prostate-specific antigen promoter, a RNA polymerase II promoter. Our data demonstrate androgen-dependent and tissue-specific siRNA-mediated gene silencing in the androgen-responsive prostate cancer cell line, LNCaP. The biological significance was evidenced by altered apoptotic activity through the inhibition of the apoptosis-related regulatory gene. These results demonstrate that siRNA-mediated gene silencing from a tissue-specific RNA polymerase II promoter could be a potential tool for tissue-specific gene therapy.

Published 2 November 2004 in Cancer Res, 64(21): 7661-3.
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Prostate Cancer Research Today Archive:

Volume 1 (2004)
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Volume 2 (2005)
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Prostate Cancer Books

Do No Harm: How a Magic Bullet for Prostate Cancer Became a Medical Quandary

Do No Harm: How a Magic Bullet for Prostate Cancer Became a Medical Quandary