2007
DOI: 10.1016/j.ygyno.2006.08.033
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Voltage-gated K+ channels are associated with cell proliferation and cell cycle of ovarian cancer cell

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Cited by 30 publications
(23 citation statements)
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“…Glibenclamide was the first second-generation sulfonylurea drug, and it functions by targeting sulfonylurea receptors (SURs). To date, a number of studies have indicated that glibenclamide can inhibit the growth of various types of cancer (51)(52)(53)(54); however, the antitumor mechanisms have not been fully elucidated. In recent years, certain studies have focused on potassium (K + ) channels, which are involved in physiological cellular functions, including insulin release, cell proliferation, and apoptosis.…”
Section: Selection Comparability Outcome ----------------------------mentioning
confidence: 99%
“…Glibenclamide was the first second-generation sulfonylurea drug, and it functions by targeting sulfonylurea receptors (SURs). To date, a number of studies have indicated that glibenclamide can inhibit the growth of various types of cancer (51)(52)(53)(54); however, the antitumor mechanisms have not been fully elucidated. In recent years, certain studies have focused on potassium (K + ) channels, which are involved in physiological cellular functions, including insulin release, cell proliferation, and apoptosis.…”
Section: Selection Comparability Outcome ----------------------------mentioning
confidence: 99%
“…For example, breast cancer cells (and probably many others) hyperpolarize during their passage through G0/G1 and into S phase by an increase in the potassium conductance of the membrane [18]. Inhibitors of voltage-gated potassium channels are therefore inhibitors of cell cycle progression in many cell culture models, like prostate [19,20], breast [21,22], colon [23,24] oral squamous [25,26], uterine [27], gastric [28], ovarian cancer [29] or gliomas [30]. In theory, all these tumor types would be susceptible to treatment with blockers of the particular respective potassium channel.…”
Section: Key Termsmentioning
confidence: 99%
“…Such an effect has been observed with treatment with nitric oxide donors [122] and dexamethasone [123]; in both cases, a concomitant increased K Ca 1.1 activity has been reported. In fact, the channel activator NS-1619 co-infusion with temozolomide and trastuzumab resulted in enhanced drug delivery to brain tumor cells [124] future science group on proliferation, pharmacological inhibition of the channel led to conflicting results probably depending on tumor type; in some cases, it impaired proliferation [125,126] but in others it had no effect [29,127,128].…”
Section: K Ca Channelsmentioning
confidence: 99%
“…Altered expression of a diversity of K + channels in human breast cancer cells, in human astrocytomas and glioblastomas, and in human ovarian cells including SKOV-3 have been documented in distinct cell models 11, 12 . Although ion channel activation through purinergic receptor stimulation is a well-known phenomenon, its role in cancer has not been thoroughly analyzed.…”
Section: Introductionmentioning
confidence: 99%