
Potassium ion (K+) channels are known to play a key role in breast cancer proliferation.We investigated the expression of Kv1.3 voltage-gated K+ channels in 60 human breast cancer specimens by immunohistochemistry. The effects of K+ channel-blockers on cellular proliferation were examined in vitro.No immunostaining was observed in 4 normal human breast specimens. Eighteen (30%) breast cancer specimens showed high, 35 (58%) moderate and 7 (12%) low Kv1.3 staining in the epithelial compartment. Minoxidil (K+ channel-opener) stimulated growth of MCF-7 human breast cancer cells (maximal approximately 60% at 10 micrograms/mL). K+ channel-blockers, dequalinium and amiodarone, had marked inhibitory effects on MCF-7 proliferation (> 90% inhibition at 1.5 micrograms/mL). Importantly, amiodarone and dequalinium potentiated the growth-inhibitory effects of tamoxifen on human breast (MCF-7, MDA-MB-231) as well as prostate (PC3, MDA-PCA-2B) and colon (Colo320DM, SW1116) cancer cell lines.Investigation of combination therapy with tamoxifen and K+ channel-blockers is warranted.
Potassium Channels, Amiodarone, Breast Neoplasms, Drug Synergism, Immunohistochemistry, Tamoxifen, Dequalinium, Antineoplastic Combined Chemotherapy Protocols, Glyburide, Minoxidil, Potassium Channel Blockers, Tumor Cells, Cultured, Humans, Cell Division
Potassium Channels, Amiodarone, Breast Neoplasms, Drug Synergism, Immunohistochemistry, Tamoxifen, Dequalinium, Antineoplastic Combined Chemotherapy Protocols, Glyburide, Minoxidil, Potassium Channel Blockers, Tumor Cells, Cultured, Humans, Cell Division
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