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10.1016/j.tibs.2016.04.005

http://scihub22266oqcxt.onion/10.1016/j.tibs.2016.04.005
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C4930368!4930368!27174209
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suck abstract from ncbi


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pmid27174209      Trends+Biochem+Sci 2016 ; 41 (7): 621-32
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  • Biochemical Basis Underlying Sestrins? Physiological Activities #MMPMID27174209
  • Ho A; Cho CS; Namkoong S; Cho US; Lee JH
  • Trends Biochem Sci 2016[Jul]; 41 (7): 621-32 PMID27174209show ga
  • Excessive accumulation of reactive oxygen species (ROS) and chronic activation of mechanistic target of rapamycin (mTOR) complex 1 (mTORC1) are well-characterized promoters of aging and age-associated degenerative pathologies. Sestrins, a family of highly conserved stress-inducible proteins, are important negative regulators of both ROS and mTORC1 signaling pathways; however, the mechanistic basis of how Sestrins suppress these pathways remains elusive. In the past couple of years, breakthrough discoveries about Sestrin signaling and its molecular nature have deeply heightened our biochemical understanding of Sestrin function. These discoveries have also uncovered new potential therapeutic strategies that may eventually enable us to attenuate aging and age-associated diseases.
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