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Autophagy Suppresses RIP Kinase-Dependent Necrosis Enabling Survival to mTOR Inhibition

Author(s): Bray, Kevin; Mathew, Robin; Lau, Alexandria; Kamphorst, Jurre J; Fan, Jing; et al

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Abstract: mTOR inhibitors are used clinically to treat renal cancer but are not curative. Here we show that autophagy is a resistance mechanism of human renal cell carcinoma (RCC) cell lines to mTOR inhibitors. RCC cell lines have high basal autophagy that is required for survival to mTOR inhibition. In RCC4 cells, inhibition of mTOR with CCI-779 stimulates autophagy and eliminates RIP kinases (RIPKs) and this is blocked by autophagy inhibition, which induces RIPK- and ROS-dependent necroptosis in vitro and suppresses xenograft growth. Autophagy of mitochondria is required for cell survival since mTOR inhibition turns off Nrf2 antioxidant defense. Thus, coordinate mTOR and autophagy inhibition leads to an imbalance between ROS production and defense, causing necroptosis that may enhance cancer treatment efficacy.
Publication Date: 26-Jul-2012
Electronic Publication Date: 26-Jul-2012
Citation: Bray, Kevin, Mathew, Robin, Lau, Alexandria, Kamphorst, Jurre J, Fan, Jing, Chen, Jim, Chen, Hsin-Yi, Ghavami, Anahita, Stein, Mark, DiPaola, Robert S, Zhang, Donna, Rabinowitz, Joshua D, White, Eileen. (2012). Autophagy Suppresses RIP Kinase-Dependent Necrosis Enabling Survival to mTOR Inhibition. PLoS ONE, 7 (7), e41831 - e41831. doi:10.1371/journal.pone.0041831
DOI: doi:10.1371/journal.pone.0041831
EISSN: 1932-6203
Pages: e41831 - e41831
Type of Material: Journal Article
Journal/Proceeding Title: PLoS ONE
Version: Final published version. This is an open access article.

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