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Boston, Mass. -- Keeping cholesterol levels in check may not only benefit heart health, but may also delay the progression of prostate cancer, suggests a study from Children's Hospital Boston. When mice with human prostate tumors were fed a no-cholesterol diet in combination with the cholesterol-lowering drug ezetimibe (Zetia, Schering-Plough), tumor growth was slowed.
The study, published in the March issue of The American Journal of Pathology, also found dramatic reductions in tumor angiogenesis–-blood-vessel growth within the tumors--in the mice with the lowest cholesterol levels, suggesting that ezetimibe retards prostate tumor growth at least in part by inhibiting tumor angiogenesis.
The researchers compared four groups of animals--two fed the high-cholesterol diet, with or without ezetimibe, and two fed a no-cholesterol diet, with or without the drug. "We were initially interested to find out whether raising cholesterol would accelerate the rate of tumor growth and whether reducing cholesterol would reduce the growth of tumors," says Keith Solomon, PhD, of the Departments of Orthopedic Surgery and Urology at Children's, and the paper's first author.
Two weeks after tumor implantation, tumors were largest in the animals fed the high-cholesterol diet (averaging 0.88 grams per tumor site), and smallest in those on the no-cholesterol diet plus the drug (averaging 0.63 grams per tumor site).
But there was also a marked difference in angiogenesis. "The thing that caught my attention almost immediately was that when we were harvesting the tumors, there was a great deal more blood in some of the tumors than others," says Solomon. "I didn't even know which groups the tumors were coming from. Then we started to look at this, and found some real group differences that went along with the growth curves."
Staining of the tumors for the endothelial cells that line blood vessel walls showed there was approximately 50 percent more tumor angiogenesis in the untreated high-cholesterol group than in the groups receiving ezetimibe, regardless of which diet they were on. Higher levels of cholesterol correlated with increased angiogenesis.
"This was something we did not anticipate at the beginning of this study," says Solomon. "We hypothesized that the tumors would be bigger or smaller based on the diet and the drug, but we did not hypothesize that it would be related to the degree of angiogenesis."
"The anti-angiogenic effect of cholesterol lowering implies that these findings may have relevance to other tumor types, " says Michael Freeman, PhD, of Children's Department of Urology, senior author of the study.
Cholesterol is synthesized in all areas of the body, but the prostate makes it at a relatively high rate and loses the ability to control cholesterol levels as the body ages. High-cholesterol diets likely contribute to the excess cholesterol in the aging prostate, and may exacerbate disease incidence and progression, Solomon says. Prostate tumors have been shown to contain significant amounts of cholesterol.
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