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自噬及自噬相关蛋白5在肿瘤早期发生中的保护作用

Protective role of autophagy and autophagy-related protein 5 in early tumorigenesis.

作者信息

Liu He, He Zhaoyue, Simon Hans-Uwe

机构信息

Institute of Pharmacology, University of Bern, Friedbuehlstrasse 49, 3010, Bern, Switzerland.

出版信息

J Mol Med (Berl). 2015 Feb;93(2):159-64. doi: 10.1007/s00109-014-1241-3. Epub 2014 Dec 23.

Abstract

Autophagy, a fundamental cellular catabolic process, is involved in the development of numerous diseases including cancer. Autophagy seems to have an ambivalent impact on tumor development. While increasing evidence indicates a cytoprotective role for autophagy that can contribute to resistance against chemotherapy and even against the adverse, hypoxic environment of established tumors, relatively few publications focus on the role of autophagy in early tumorigenesis. However, the consensus is that autophagy is inhibitory for the genesis of tumors. To understand this apparent contradiction, more detailed information about the roles of the individual participants in autophagy is needed. This review will address this topic with respect to autophagy-related protein 5 (ATG5), which in several lines of investigation has been ascribed special significance in the autophagic pathway. Furthermore, it was recently shown that an ATG5 deficiency in melanocytes interferes with oncogene-induced senescence, thus promoting melanoma tumorigenesis. Similarly, an ATG5 deficiency resulted in tumors of the lung and liver in experimental mouse models. Taken together, these findings indicate that ATG5 and the autophagy to which it contributes are essential gatekeepers restricting early tumorigenesis in multiple tissues.

摘要

自噬是一种基本的细胞分解代谢过程,参与包括癌症在内的多种疾病的发展。自噬似乎对肿瘤发展具有矛盾的影响。虽然越来越多的证据表明自噬具有细胞保护作用,可有助于抵抗化疗,甚至抵抗已形成肿瘤的不利缺氧环境,但相对较少的出版物关注自噬在早期肿瘤发生中的作用。然而,目前的共识是自噬对肿瘤发生具有抑制作用。为了理解这一明显的矛盾,需要更多关于自噬中各个参与者作用的详细信息。本综述将针对自噬相关蛋白5(ATG5)探讨这一主题,在多项研究中,ATG5在自噬途径中被赋予了特殊意义。此外,最近有研究表明,黑素细胞中ATG5的缺乏会干扰癌基因诱导的衰老,从而促进黑色素瘤的肿瘤发生。同样,在实验小鼠模型中,ATG5的缺乏导致了肺癌和肝癌。综上所述,这些发现表明ATG5及其所参与的自噬是限制多个组织早期肿瘤发生的关键守门人。

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