CaT1 expression correlates with tumor grade in prostate cancer

被引:143
作者
Peng, JB
Zhuang, LY
Berger, UV
Adam, RM
Williams, BJ
Brown, EM
Hediger, MA
Freeman, MR
机构
[1] Harvard Univ, Inst Med, Sch Med, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Dept Med, Membrane Biol Program, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Dept Med, Renal Div, Boston, MA 02115 USA
[4] Brigham & Womens Hosp, Dept Med, Endocrine Hypertens Div, Boston, MA 02115 USA
[5] Childrens Hosp, Dept Urol, Urol Lab, Boston, MA 02115 USA
[6] Harvard Univ, Sch Med, Dept Surg, Boston, MA 02115 USA
[7] Louisiana State Univ, Med Ctr, Dept Urol, Shreveport, LA 71130 USA
关键词
calcium signaling; calcium channel; androgen withdrawal; prostate cancer progression; apoptosis;
D O I
10.1006/bbrc.2001.4638
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
Ca2+ signaling is important for growth and survival of prostatic carcinoma (PCa) cells. Here we report that the gene for CaT1, a channel protein highly selective for Ca2+, is expressed at high levels in human PCa and in the LNCaP PCa cell line, CaT1 mRNA levels were elevated in PCa specimens in comparison to benign prostatic hyperplasia (BPH) specimens and positively correlated with Gleason grade in a PCa series. CaT1 mRNA was suppressed by androgen and was induced by a specific androgen receptor antagonist in LNCaP eels, suggesting that the gene is negatively regulated by androgen. These findings are the first to implicate a Ca2+ channel in PCa progression and suggest that CaT1 may be a novel target for therapy. (C) 2001 Academic Press.
引用
收藏
页码:729 / 734
页数:6
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