Literature DB >> 17146446

KCNMA1 gene amplification promotes tumor cell proliferation in human prostate cancer.

M Bloch1, J Ousingsawat, R Simon, P Schraml, T C Gasser, M J Mihatsch, K Kunzelmann, L Bubendorf.   

Abstract

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.

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Year:  2006        PMID: 17146446     DOI: 10.1038/sj.onc.1210036

Source DB:  PubMed          Journal:  Oncogene        ISSN: 0950-9232            Impact factor:   9.867


  64 in total

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5.  State-dependent FRET reports calcium- and voltage-dependent gating-ring motions in BK channels.

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9.  Glioma big potassium channel expression in human cancers and possible T cell epitopes for their immunotherapy.

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10.  The regulation of miRNA-211 expression and its role in melanoma cell invasiveness.

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