T-type Ca2+ channel blockers suppress the growth of human cancer cells
- Authors
- Heo, Jae Ho; Seo, Han Na; Choe, Yun Jeong; Kim, Sujin; Oh, Chun Rim; Kim, Young Deuk; Rhim, Hyewhon; Choo, Dong Joon; Kim, Jungahn; Lee, Jae Yeol
- Issue Date
- 2008-07-15
- Publisher
- PERGAMON-ELSEVIER SCIENCE LTD
- Citation
- BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.18, no.14, pp.3899 - 3901
- Abstract
- In order to further clarify the role of T-type Ca2+ channels in cell proliferation, we have measured the growth inhibition of human cancer cells by using our potent T-type Ca2+ channel blockers. As a result, KYS05090, a most potent T-type Ca2+ channel blocker, was found to be as potent as doxorubicin against some human cancer cells without acute toxicity. Therefore, this letter provides the biological results that T-type calcium channel is important in regulating the important cellular phenotype transition leading to cell proliferation, and thus novel T-type Ca2+ channel blocker presents new prospects for cancer treatment. (C) 2008 Elsevier Ltd. All rights reserved.
- Keywords
- BIOLOGICAL EVALUATION; CALCIUM-CHANNELS; IN-VITRO; INHIBITION; PROLIFERATION; MIBEFRADIL; EXPRESSION; DRUG; BIOLOGICAL EVALUATION; CALCIUM-CHANNELS; IN-VITRO; INHIBITION; PROLIFERATION; MIBEFRADIL; EXPRESSION; DRUG; T-type calcium channel blocker; 3,4-dihydroquinazoline; doxorubicin; anti-cancer
- ISSN
- 0960-894X
- URI
- https://pubs.kist.re.kr/handle/201004/133320
- DOI
- 10.1016/j.bmcl.2008.06.034
- Appears in Collections:
- KIST Article > 2008
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