KCNMA1 gene amplification promotes tumor cell proliferation in human prostate cancer

被引:110
作者
Bloch, M.
Ousingsawat, J.
Simon, R.
Schraml, P.
Gasser, T. C.
Mihatsch, M. J.
Kunzelmann, K.
Bubendorf, L.
机构
[1] Univ Basel Hosp, Inst Pathol, CH-4003 Basel, Switzerland
[2] Univ Regensburg, Dept Physiol, D-8400 Regensburg, Germany
[3] Univ Basel, Dept Urol, Liestal, Switzerland
关键词
prostate cancer; progression; amplification; BK channel; KCNMA1;
D O I
10.1038/sj.onc.1210036
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
Molecular mechanisms of prostate cancer progression are poorly understood. Here, we studied gene amplification of the large conductance calcium-activated potassium channel alpha subunit (KCNMA1), which is located at the chromosomal region 10q22. Fluorescence in situ hybridization ( FISH) revealed KCNMA1 amplification in 16% of 119 late-stage human prostate cancers and in the hormone-insensitive prostate cancer cell line PC-3. In contrast, KCNMA1 amplification was absent in 33 benign controls, 32 precursor lesions and in 105 clinically organ-confined prostate cancers. Amplification was associated with mRNA and protein overexpression as well as increased density of BK channel protein and beta-estradiol-insensitive BK currents in PC-3 cells as compared to non-amplified control cell lines. Specific blockade of BK channels by iberiotoxin or RNA(i) significantly inhibited K+ currents and growth of PC-3 cells. The data demonstrate that 10q22 amplification drives KCNMA1 expression and cell proliferation. Thus, KCNMA1 qualifies as a promising diagnostic and therapeutic target in patients with prostate cancer.
引用
收藏
页码:2525 / 2534
页数:10
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