2-(3-fluorophenyl)-6-methoxyl-4-oxo-1,4-dihydroquinoline-3-carboxylic acid (YJC-1) induces mitotic phase arrest in A549 cells

被引:25
作者
Hsu, Mei-Hua
Chen, Chun-Jen
Kuo, Sheng-Chu
Chung, Jing-Gung
Lai, Ya-Yun
Teng, Che-Ming
Pan, Shiow-Lin
Huang, Li-Jiau
机构
[1] China Med Univ, Grad Inst Pharmaceut Chem, Taichung 40421, Taiwan
[2] China Med Univ, Grad Inst Med Sci, Taichung 40421, Taiwan
[3] Chung Shan Med Univ, Dept Appl Chem, Taichung, Taiwan
[4] Natl Taiwan Univ, Coll Med, Inst Pharmacol, Taipei, Taiwan
关键词
2-phenyl-4-quinolone (2-PQ); 2-(3-fluorophenyl)-6-methoxyl-4-oxo-1,4-dihydroquinoline-3-carboxylic acid (YJC-1); mitotic phase arrest; microtubule polymerization; p21(Cip1/Waf1); A549; cells;
D O I
10.1016/j.ejphar.2006.12.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A 2-phenyl-4-quinolone (2-PQ) derivative, 2-(3-fluorophenyl)-6-methoxyl-4-oxo-1,4-dihydroquinoline-3-carboxylic acid (YJC-1), was synthesized in our laboratory. In this study, we delineated the growth-inhibitory effect of YJC-1 in human lung carcinoma A549 cells. YJC-1 inhibited cell growth with an IC50 value of about 4.8 mu M via microtubule polymerization, causing growth arrest in the mitotic phase. Immunoblotting analysis revealed a dramatic induction of cyclin-dependent kinase (CDK) inhibitor p21(cip/Waf1) and down-regulation of Cdc25C phosphatase to inhibit the protein expression of cyclin B 1 and CDK1. We also found that YJC-1 induced a profound time-dependent elevation in p21(Cip/Waf1) gene expression in comparison with the negative control. In vivo, we also found that YJC-1 significantly suppressed tumor growth in mice inoculated with A549 cells. These findings suggest that YJC-1 can suppress A549 cell growth via mitotic phase arrest. (c) 2007 Published by Elsevier B.V.
引用
收藏
页码:14 / 20
页数:7
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