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- W4313361856 endingPage "98" @default.
- W4313361856 startingPage "98" @default.
- W4313361856 abstract "Reactive oxygen species (ROS), products of normal cellular metabolism, play an important role in signal transduction. Autophagy is an intracellular degradation process in response to various stress conditions, such as nutritional deprivation, organelle damage and accumulation of abnormal proteins. ROS and autophagy both exhibit double-edged sword roles in the occurrence and development of cancer. Studies have shown that oxidative stress, as the converging point of these stimuli, is involved in the mechanical regulation of autophagy process. The regulation of ROS on autophagy can be roughly divided into indirect and direct methods. The indirect regulation of autophagy by ROS includes post-transcriptional and transcriptional modulation. ROS-mediated post-transcriptional regulation of autophagy includes the post-translational modifications and protein interactions of AMPK, Beclin 1, PI3K and other molecules, while transcriptional regulation mainly focuses on p62/Keap1/Nrf2 pathway. Notably, ROS can directly oxidize key autophagy proteins, such as ATG4 and p62, leading to the inhibition of autophagy pathway. In this review, we will elaborate the molecular mechanisms of redox regulation of autophagy in cancer, and discuss ROS- and autophagy-based therapeutic strategies for cancer treatment." @default.
- W4313361856 created "2023-01-06" @default.
- W4313361856 creator A5002625267 @default.
- W4313361856 creator A5016414843 @default.
- W4313361856 creator A5021333880 @default.
- W4313361856 creator A5067262292 @default.
- W4313361856 date "2022-12-29" @default.
- W4313361856 modified "2023-09-30" @default.
- W4313361856 title "Redox Regulation of Autophagy in Cancer: Mechanism, Prevention and Therapy" @default.
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