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尼古丁对细胞凋亡的抑制表明其在肿瘤促进过程中发挥作用。

Nicotine inhibition of apoptosis suggests a role in tumor promotion.

作者信息

Wright S C, Zhong J, Zheng H, Larrick J W

机构信息

Palo Alto Institute of Molecular Medicine, Mountain View, CA 94043.

出版信息

FASEB J. 1993 Aug;7(11):1045-51.

PMID:8370474
Abstract

Recent evidence indicates that cell death through apoptosis may be an important mechanism to prevent tumor development. Therefore, agents that inhibit apoptosis may function as tumor promoters. The purpose of this study was to determine the effects of nicotine on the process of apoptosis. The results demonstrate that nicotine inhibits apoptosis induced by diverse stimuli including tumor necrosis factor (TNF), UV light, chemotherapeutic drugs, and calcium ionophore. This phenomenon was observed in normal and transformed cells derived from a variety of species and tissues, including tumor cell types related to tobacco use. The major nicotine metabolite, cotinine, also inhibited apoptosis, whereas N-nitrosodiethylamine, a carcinogen found in tobacco, was without effect. Therefore, nicotine-mediated inhibition of apoptosis may contribute to the pathogenesis of tobacco-related cancer as well as decrease the efficacy of cancer therapies.

摘要

最近的证据表明,通过凋亡导致的细胞死亡可能是预防肿瘤发生的重要机制。因此,抑制凋亡的药物可能起到肿瘤促进剂的作用。本研究的目的是确定尼古丁对凋亡过程的影响。结果表明,尼古丁可抑制由多种刺激诱导的凋亡,这些刺激包括肿瘤坏死因子(TNF)、紫外线、化疗药物和钙离子载体。在源自多种物种和组织的正常细胞和转化细胞中均观察到了这一现象,包括与烟草使用相关的肿瘤细胞类型。尼古丁的主要代谢产物可替宁也抑制凋亡,而烟草中发现的一种致癌物N-亚硝基二乙胺则没有此作用。因此,尼古丁介导的凋亡抑制可能促成与烟草相关癌症的发病机制,并降低癌症治疗的疗效。

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