Bloch M, Ousingsawat J, Simon R, Schraml P, Gasser T C, Mihatsch M J, Kunzelmann K, Bubendorf L
Institute for Pathology, University Hospital Basel, Basel, Switzerland.
Oncogene. 2007 Apr 12;26(17):2525-34. doi: 10.1038/sj.onc.1210036. Epub 2006 Dec 4.
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.
前列腺癌进展的分子机制目前仍知之甚少。在此,我们研究了位于染色体区域10q22的大电导钙激活钾通道α亚基(KCNMA1)的基因扩增情况。荧光原位杂交(FISH)显示,在119例晚期人类前列腺癌中有16%以及在激素不敏感的前列腺癌细胞系PC-3中存在KCNMA1扩增。相比之下,在33例良性对照、32例癌前病变以及105例临床器官局限性前列腺癌中未发现KCNMA1扩增。与未扩增的对照细胞系相比,扩增与PC-3细胞中mRNA和蛋白的过表达以及BK通道蛋白密度增加和β-雌二醇不敏感的BK电流增加有关。iberiotoxin或RNA干扰(RNAi)对BK通道的特异性阻断显著抑制了PC-3细胞的K(+)电流和生长。数据表明,10q22扩增驱动KCNMA1表达和细胞增殖。因此,KCNMA1有望成为前列腺癌患者的诊断和治疗靶点。