Proliferative inhibition, cell-cycle dysregulation, and induction of apoptosis by ursolic acid in human non-small cell lung cancer A549 cells

被引:201
作者
Hsu, YL
Kuo, PL
Lin, CC
机构
[1] Kaohsiung Med Univ, Coll Pharm, Grad Inst Nat Prod, Kaohsiung 807, Taiwan
[2] Chia Nan Univ Pharmacol & Sci, Dept Biotechnol, Tainan 717, Taiwan
关键词
ursolic acid; p53; cell cycle; Fas/APO-1; FasL; apoptosis;
D O I
10.1016/j.lfs.2004.04.027
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Ursolic acid (UA) is a pentacyclic triterpene compound isolated from many types of medicinal plants and is present in human diet. It has been reported to possess a wide range of pharmacological properties, and is one of the most promising chemopreventive agents for cancer. Here, we report that UA inhibits the cell proliferation of human lung cancer cell line A549 and provide a molecular understanding of this effect. The results showed that UA blocked cell cycle progression in the G1 phase that was associated with a marked decrease in the protein expression of cyclin D1, D2, and E and their activating partner cdk2, 4, and 6 with concomitant induction of p21/WAF1. This accumulation of p21/WAF1 might be through a p53-dependent manner. Further, UA treatment also resulted in the triggering of apoptosis as determined by DNA fragmentation assay. This effect was found to correlate with the up-regulation of Fas/APO-1, Fas ligand, and Bax, and down-regulation of NF-kappaB, Bcl-2, and Bcl-X-L. Taken together, our study indicated that UA might be a potential chemopreventive agent for lung cancer. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:2303 / 2316
页数:14
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