A veterinary pathologist on the study, first author Aaron Sargeant, graduate research associate in veterinary biosciences, was intrigued that adenomas occurred in the treated animals. Adenomas are not commonly found to be part of prostate-cancer development in this system, he says. This drug appears to shift tumor progression from its usual aggressive course to a more benign direction.
For this study, Chen, Sargeant, Clinton and their colleagues used a strain of transgenic mice that develops PIN at about six weeks of age, then progresses to advanced prostate cancer by 24 to 32 weeks.
The researchers added the drug to the diet of 23 of the cancer-prone mice beginning at six weeks of age, when the animals develop the precancerous condition, and continued the treatment for 18 weeks.
They then examined the animals. Of the treated mice, one showed signs of early stage cancer, but 12 still had only the precancerous condition and 10 had adenomas.
In contrast, 17 of 23 control animals developed advanced prostate cancer, two had early stage cancer, three had the precancerous condition and one an adenoma.
Experiments using a nontransgenic strain of the same mouse they do not develop prostate cancer showed that the degeneration of the testicles that accompanied the drug treatment was reversible when the drug treatment stops.
Chen noted that 186,320 cases of prostate cancer are expected this year, with 28,660 deaths from the disease. Our findings are very exciting, considering that an agent capable of reducing prostate-cancer risk by only 10 percent could prevent 18,600 cases of the disease in the United States each year, Chen says.
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| Contact: Darrell E. Ward darrell.ward@osumc.edu 614-293-3737 Ohio State University Medical Center Source:Eurekalert |