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Mechanisms of tumor-promoting activities of nicotine in lung cancer: synergistic effects of cell membrane and mitochondrial nicotinic acetylcholine receptors

机译:肺癌中尼古丁促进肿瘤活动的机制:细胞膜和线粒体烟碱型乙酰胆碱受体的协同作用

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摘要

BackgroundOne of the major controversies of contemporary medicine is created by an increased consumption of nicotine and growing evidence of its connection to cancer, which urges elucidation of the molecular mechanisms of oncogenic effects of inhaled nicotine. Current research indicates that nicotinergic regulation of cell survival and death is more complex than originally thought, because it involves signals emanating from both cell membrane (cm)- and mitochondrial (mt)-nicotinic acetylcholine receptors (nAChRs). In this study, we elaborated on the novel concept linking cm-nAChRs to growth promotion of lung cancer cells through cooperation with the growth factor signaling, and mt-nAChRs — to inhibition of intrinsic apoptosis through prevention of opening of mitochondrial permeability transition pore (mPTP).
机译:背景技术现代医学的主要争议之一是由于尼古丁的消费增加和与癌症的联系不断增加的证据,这促使人们阐明吸入尼古丁的致癌作用的分子机制。目前的研究表明,对细胞存活和死亡的烟碱能调节比最初想像的要复杂,因为它涉及从细胞膜(cm)和线粒体(mt)的烟碱乙酰胆碱受体(nAChRs)发出的信号。在这项研究中,我们详细阐述了通过将cm-nAChRs与生长因子信号传导和mt-nAChRs协同作用,将cm-nAChRs与肺癌细胞的生长促进联系起来的新概念,即通过防止线粒体通透性过渡孔(mPTP)的开放来抑制固有凋亡。 )。

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