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Bcl-2家族成员在肿瘤发生中的作用。

The role of Bcl-2 family members in tumorigenesis.

作者信息

Kirkin Vladimir, Joos Stefan, Zörnig Martin

机构信息

Georg-Speyer-Haus, Paul-Ehrlich-Strasse 42-44, D-60596 Frankfurt, Germany.

出版信息

Biochim Biophys Acta. 2004 Mar 1;1644(2-3):229-49. doi: 10.1016/j.bbamcr.2003.08.009.

Abstract

The Bcl-2 family consists of about 20 homologues of important pro- and anti-apoptotic regulators of programmed cell death. The established mode of function of the individual members is to either preserve or disturb mitochondrial integrity, thereby inducing or preventing release of apoptogenic factors like Cytochrome c (Cyt c) from mitochondria. Recent findings also indicate further Bcl-2-controlled mitochondria-independent apoptosis pathways. Bcl-2 represents the founding member of the new and growing class of cell death inhibiting oncoproteins. In this review, we try to briefly summarize current models of Bcl-2 family function and to outline the work demonstrating the influence of deregulated Bcl-2 family member expression on tumorigenesis and cancer therapy. Since several Bcl-2 homologues, in addition to influencing apoptotic behaviour, also impinge on cell cycle progression, we discuss possible implications of this additional role for the expression of Bcl-2 family members in tumor cells.

摘要

Bcl-2家族由约20种细胞程序性死亡的重要促凋亡和抗凋亡调节因子的同源物组成。各成员既定的功能模式是维持或破坏线粒体完整性,从而诱导或阻止诸如细胞色素c(Cyt c)等凋亡因子从线粒体释放。最近的研究结果还表明存在其他由Bcl-2控制的不依赖线粒体的凋亡途径。Bcl-2是新出现且不断增加的一类抑制细胞死亡的癌蛋白中的首个成员。在本综述中,我们试图简要总结Bcl-2家族功能的当前模型,并概述证明Bcl-2家族成员表达失调对肿瘤发生和癌症治疗影响的研究工作。由于几种Bcl-2同源物除了影响凋亡行为外,还会影响细胞周期进程,因此我们讨论了这一额外作用对肿瘤细胞中Bcl-2家族成员表达的可能影响。

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