Nicotine prevents the apoptosis induced by menadione in human lung cancer cells

被引:26
作者
Zhang, T
Lu, H
Shang, X
Tian, YH
Zheng, CY
Wang, SW
Cheng, HH [1 ]
Zhou, RJ
机构
[1] Wuhan Univ, Coll Life Sci, Dept Genet, Wuhan 430072, Peoples R China
[2] Wuhan Univ, Coll Life Sci, Ctr Dev Biol, Wuhan 430072, Peoples R China
[3] Wuhan Univ, Coll Life Sci, Ctr Type Culture Collect, Wuhan 430072, Peoples R China
[4] Gen Hosp PLA, Inst Geriatr Cardiol, Beijing 100853, Peoples R China
基金
中国国家自然科学基金;
关键词
apoptosis; lung cancer; NF-kappa B; tobacco;
D O I
10.1016/j.bbrc.2006.02.047
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Approximately 50% of long-term cigarette smokers die prematurely from the adverse effects of smoking, including on lung cancer and other illnesses. Nicotine is a main component in tobacco and has been implicated as a potential factor in the pathogenesis of human lung cancer. However, the mechanism of nicotine action in the development of lung cancer remains largely unknown. In the present study, we designed a nicotine-apoptosis system, by pre-treatment of nicotine making lung cancer cell A549 to be in a physiological nicotine environment, and observed that nicotine promoted cell proliferation and prevented the menadione-induced apoptosis, and exerts its role of anti-apoptosis by shift of apoptotic stage induced by menadione from late apoptotic stage to early apoptotic stage, in which NF-kappa B was up-regulated. Interference analysis of NF-kappa B in A549 cells showed that knock down of NF-kappa B resulted in apoptosis promotion and counteracted the protective effect of nicotine. The findings suggest that nicotine has potential effect in lung cancer genesis, especially in patients with undetectable early tumor development and development of specific NF-kappa B inhibitors would represent a potentially exciting new pharmacotherapy for tobacco-related lung cancer. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:928 / 934
页数:7
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