自噬
生物
癌变
细胞生物学
程序性细胞死亡
基因组不稳定性
背景(考古学)
癌细胞
癌症研究
癌症
转移
细胞凋亡
DNA损伤
活性氧
机制(生物学)
遗传学
DNA
古生物学
哲学
认识论
作者
Prashanta Kumar Panda,Subhadip Mukhopadhyay,Durgesh Nandini Das,Niharika Sinha,Prajna Paramita Naik,Sujit K. Bhutia
标识
DOI:10.1016/j.semcdb.2015.02.013
摘要
Autophagy in cancer is an intensely debated concept in the field of translational research. The dual nature of autophagy implies that it can potentially modulate the pro-survival and pro-death mechanisms in tumor initiation and progression. There is a prospective molecular relationship between defective autophagy and tumorigenesis that involves the accumulation of damaged mitochondria and protein aggregates, which leads to the production of reactive oxygen species (ROS) and ultimately causes DNA damage that can lead to genomic instability. Moreover, autophagy regulates necrosis and is followed by inflammation, which limits tumor metastasis. On the other hand, autophagy provides a survival advantage to detached, dormant metastatic cells through nutrient fueling by tumor-associated stromal cells. Manipulating autophagy for induction of cell death, inhibition of protective autophagy at tissue-and context-dependent for apoptosis modulation has therapeutic implications. This review presents a comprehensive overview of the present state of knowledge regarding autophagy as a new approach to treat cancer.
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