Cell
Volume 154, Issue 4, 15 August 2013, Pages 859-874
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Article
Inhibition of mTORC1 by Astrin and Stress Granules Prevents Apoptosis in Cancer Cells

https://doi.org/10.1016/j.cell.2013.07.031Get rights and content
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Highlights

  • Astrin is a negative regulator of mTORC1 signaling

  • Astrin recruits the mTORC1 component raptor to SGs

  • Astrin restricts mTORC1 association and activity upon metabolic and redox stimuli

  • Astrin mediates antiapoptotic SG functions by preventing mTORC1 hyperactivation

Summary

Mammalian target of rapamycin complex 1 (mTORC1) controls growth and survival in response to metabolic cues. Oxidative stress affects mTORC1 via inhibitory and stimulatory inputs. Whereas downregulation of TSC1-TSC2 activates mTORC1 upon oxidative stress, the molecular mechanism of mTORC1 inhibition remains unknown. Here, we identify astrin as an essential negative mTORC1 regulator in the cellular stress response. Upon stress, astrin inhibits mTORC1 association and recruits the mTORC1 component raptor to stress granules (SGs), thereby preventing mTORC1-hyperactivation-induced apoptosis. In turn, balanced mTORC1 activity enables expression of stress factors. By identifying astrin as a direct molecular link between mTORC1, SG assembly, and the stress response, we establish a unifying model of mTORC1 inhibition and activation upon stress. Importantly, we show that in cancer cells, apoptosis suppression during stress depends on astrin. Being frequently upregulated in tumors, astrin is a potential clinically relevant target to sensitize tumors to apoptosis.

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14

These authors contributed equally to this work

15

Present address: Center for Liver, Digestive and Metabolic Diseases, Department of Pediatrics, University of Groningen, University Medical Center Groningen, Hanzeplein 1, 9713 GZ Groningen, The Netherlands