Department of Immunology, Shandong University, School of Medicine, Shangdong, China.
Autophagy. 2013 May;9(5):743-55. doi: 10.4161/auto.24069. Epub 2013 Mar 13.
PDCD4 (programmed cell death protein 4), a suppressor of gene transcription and translation, plays a crucial inhibitory role in several types of human tumors. However, its underlying mechanisms remain unclear. Autophagy, an evolutionarily conserved catabolic process, maintains cellular homeostasis under stress conditions such as starvation and plays a crucial role in tumor initiation and progression. We report here that PDCD4 inhibits autophagy in multiple cell types both in vitro and in vivo, which in turn contributes to its tumor suppressor activity. Importantly, PDCD4 inhibits the expression of an essential autophagy related gene, ATG5 and the formation of an ATG12-ATG5 complex, and its ma3 domains are required for PDCD4-mediated inhibition of autophagy. Unlike most tumor suppressors that act as positive or dual regulators of autophagy, our findings indicate that PDCD4 negatively regulates autophagy by targeting ATG5, which provides a novel mechanism of tumor suppression.
程序性细胞死亡蛋白 4(PDCD4)是一种转录和翻译抑制因子,在多种人类肿瘤中发挥关键抑制作用。然而,其潜在机制尚不清楚。自噬是一种进化上保守的分解代谢过程,在饥饿等应激条件下维持细胞内环境稳定,在肿瘤的发生和发展中起着至关重要的作用。我们在这里报告,PDCD4 在体外和体内的多种细胞类型中均抑制自噬,这反过来又有助于其肿瘤抑制活性。重要的是,PDCD4 抑制必需的自噬相关基因 ATG5 的表达和 ATG12-ATG5 复合物的形成,其 ma3 结构域是 PDCD4 介导的自噬抑制所必需的。与大多数作为自噬的正调控或双重调控因子的肿瘤抑制因子不同,我们的研究结果表明,PDCD4 通过靶向 ATG5 负调控自噬,为肿瘤抑制提供了一种新的机制。