Structure and function of GC79/TRPS1, a novel androgen-repressible apoptosis gene

被引:34
作者
Chang, GTG [1 ]
van den Bemd, GJCM [1 ]
Jhamai, M [1 ]
Brinkmann, AO [1 ]
机构
[1] Erasmus Univ, Med Ctr, Dept Endocrinol & Reprod, NL-3000 DR Rotterdam, Netherlands
关键词
androgen-independent; apoptosis; GC79/TRPS1; prostate cancer; zinc finger protein;
D O I
10.1023/A:1013504710343
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
Expression of death-signaling genes induces many biochemical cascades resulting in elimination of cells via apoptosis or programmed cell death. GC79/TRPS1 is a novel apoptosis associated gene that encodes a multitype zinc finger GATA-type transcription factor. Expression of GC79/TRPS1 is repressed in the rat ventral prostate and significantly elevated after androgen withdrawal by castration. Castration leads to regression of the prostate caused by apoptosis of androgen-dependent prostate cells. Prostate cancer consists of androgen-dependent and androgen-independent cells. The androgen-independent cells, usually present in the prostate of advanced prostate cancer patients do not have the ability to undergo apoptosis after androgen withdrawal. GC79/TRPS1 expression in androgen-dependent prostate cancer cells is repressed by androgens, while GC79/TRPS1 expression is hardly detectable in androgen-independent prostate cancer cells under cell culture conditions. This suggests that lack of GC79/TRPS1 expression could be a mechanism for the inability to induce the apoptotic pathway in androgen-independent prostate cancer cells after androgen withdrawal. This review will focus on the current knowlegde of the structure and function of GC79/TRPS1, a novel androgen-repressible apoptosis gene.
引用
收藏
页码:13 / 21
页数:9
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