The role of vitamin D in prostate cancer

被引:55
|
作者
Zhao, XY [1 ]
Feldman, D [1 ]
机构
[1] Stanford Univ, Med Ctr, Div Endocrinol, Sch Med,Dept Med, Stanford, CA 94305 USA
关键词
prostate cancer; 1; alpha; 25(OH)(2)D-3; (calcitriol); vitamin D analogs; vitamin D receptor; androgen receptor; steroid;
D O I
10.1016/S0039-128X(00)00164-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Prostate cancer is the second leading cause of cancer deaths in men in the United States. Developing new treatment strategies is critical to improving the health of men. This article will be a general review of the field with a focus on research from our laboratory. Our research has focused on four areas in which we have pursued the possible use of 1 alpha ,25(OH)(2)D-3 and its analogs to treat prostate cancer: 1) The ability of 1 alpha ,25(OH)(2)D-3 to up-regulate androgen receptors in L.NCaP human prostate cancer cells. The implications of this finding on 1 alpha ,25(OH)(2)D-3's ability to inhibit cell growth in vivo are unclear at present. 2) The reasons for an inability of 1 alpha ,25(OH)(2)D-3 to inhibit DU 145 prostate cancer cell growth were explored. We found that combination of an imidazole drug, Liarozole, with 1 alpha ,25(OH)(2)D-3 was capable of inhibiting DU 145 cell growth. 3) A number of low-calcemic vitamin D analogs exhibit potent anti-proliferative activity on prostate cancer cells. We have developed a novel approach using the yeast two-hybrid system to screen for potent analogs. 4) The results of a clinical trial of 1 alpha ,25(OH)(2)D-3 treatment of patients with early recurrent prostate cancer. We provide preliminary evidence that 1 alpha ,25(OH)(2)D-3 may be effective in slowing the rate of PSA rise in selected cases of prostate cancer. In conclusion, we believe that 1 alpha ,25(OH)(2)D-3, has a role in the treatment and/or prevention strategies being developed for prostate cancer. However, to increase antiproliferative potency without increasing side -effects. the use of less calcemic analogs appears to be the most reasonable approach. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:293 / 300
页数:8
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