Protein kinase C μ is down-regulated in androgen-independent prostate cancer

被引:58
作者
Jaggi, M [1 ]
Rao, PS [1 ]
Smith, DJ [1 ]
Hemstreet, GP [1 ]
Balaji, KC [1 ]
机构
[1] Univ Nebraska, Med Ctr, Dept Surg, Div Urol, Omaha, NE 68198 USA
关键词
PKCp; prostate cancer; androgen independence; LNCaP cells; C4-2; cells;
D O I
10.1016/S0006-291X(03)01161-6
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
Progression to androgen independence (AI) is the main cause of death in prostate cancer. Our prior differential gene expression studies by microarray analysis in progressive prostate cancer cell line model identified dysregulation of protein kinase C mu (PKCmu) expression in prostate cancer. In this study, quantitative ribonuclease protection assay and immunoblot analysis demonstrate down regulation of PKCmu at transcription and translational level, respectively, in AI C4-2 cells compared to its parental androgen dependent (AD) LNCaP prostate cancer cells. Significantly lower PKCp kinase activity was confirmed in C4-2 cells by in vitro kinase assay. Immunohistochemical studies of prostate cancer tissue from patient progressing to AI prostate cancer demonstrated that PKCmu expression is decreased in 100% of At human prostate cancers. The consistent down regulation of PKCmu in cell line models and human prostate cancer tissues suggests a possible functionally significant role for PKCp in progression to AI in prostate cancer. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:254 / 260
页数:7
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