Versatile pharmacological actions of YC-1: anti-platelet to anticancer

被引:48
作者
Chun, YS
Yeo, EJ
Park, JW
机构
[1] Seoul Natl Univ, Coll Med, Dept Pharmacol, Seoul 110799, South Korea
[2] Seoul Natl Univ, Coll Med, Canc Res Inst, Seoul 110799, South Korea
[3] Seoul Natl Univ, Coll Med, Human Genome Res Inst, Seoul 110799, South Korea
关键词
YC-1; soluble guanylate cyclase; cyclic GMP; hypoxia-inducible factor; anticancer effect;
D O I
10.1016/j.canlet.2004.01.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Since the first article on YC-1 was published in 1994, it has been popularly used as a pharmacological tool to activate soluble guanylate cyclase and to increase cyclic GMP levels in cultured cells or isolated tissues. In terms of the pharmacological actions of YC-1, previous studies tend to be limited to its inhibition of platelet aggregation and vascular contraction. However, recent studies have demonstrated that YC-1 has versatile pharmacological effects other than the anti-platelet and vasodilatory effects. In particular, two recent reports suggest that YC-1 could be developed as a new class of anticancer agent for rapidly growing solid tumors, because it inhibits hypoxia-inducible factor 1 (HIF-1) activity, and has been reported to halt tumor growth in vivo. We here review the cyclic GMP-dependent and independent pharmacological actions of YC-1, and its anti-HIF-1, anticancer effect. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:1 / 7
页数:7
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