Liu Bo, Bao Jin-Ku, Yang Jin-Ming, Cheng Yan
School of Life Sciences, Sichuan University, Chengdu, People's Republic of China.
Chin J Cancer. 2013 Mar;32(3):113-20. doi: 10.5732/cjc.012.10010. Epub 2012 Jul 26.
Autophagy, an evolutionarily conserved lysosomal degradation process, has drawn an increasing amount of attention in recent years for its role in a variety of human diseases, such as cancer. Notably, autophagy plays an important role in regulating several survival and death signaling pathways that determine cell fate in cancer. To date, substantial evidence has demonstrated that some key autophagic mediators, such as autophagy-related genes (ATGs), PI3K, mTOR, p53, and Beclin-1, may play crucial roles in modulating autophagic activity in cancer initiation and progression. Because autophagy-modulating agents such as rapamycin and chloroquine have already been used clinically to treat cancer, it is conceivable that targeting autophagic pathways may provide a new opportunity for discovery and development of more novel cancer therapeutics. With a deeper understanding of the regulatory mechanisms governing autophagy, we will have a better opportunity to facilitate the exploitation of autophagy as a target for therapeutic intervention in cancer. This review discusses the current status of targeting autophagic pathways as a potential cancer therapy.
自噬是一种进化上保守的溶酶体降解过程,近年来因其在包括癌症在内的多种人类疾病中的作用而受到越来越多的关注。值得注意的是,自噬在调节决定癌症细胞命运的几种生存和死亡信号通路中起着重要作用。迄今为止,大量证据表明,一些关键的自噬介质,如自噬相关基因(ATG)、PI3K、mTOR、p53和Beclin-1,可能在调节癌症发生和发展过程中的自噬活性方面发挥关键作用。由于雷帕霉素和氯喹等自噬调节剂已在临床上用于治疗癌症,可以想象,靶向自噬途径可能为发现和开发更多新型癌症治疗药物提供新的机会。随着对自噬调控机制的更深入了解,我们将有更好的机会促进将自噬作为癌症治疗干预靶点的开发利用。本综述讨论了将自噬途径作为潜在癌症治疗方法的现状。