Literature DB >> 23124837

mTOR-dependent cell survival mechanisms.

Chien-Min Hung1, Luisa Garcia-Haro, Cynthia A Sparks, David A Guertin.   

Abstract

The mechanistic target of rapamycin (mTOR) kinase is a conserved regulator of cell growth, proliferation, and survival. In cells, mTOR is the catalytic subunit of two complexes called mTORC1 and mTORC2, which have distinct upstream regulatory signals and downstream substrates. mTORC1 directly senses cellular nutrient availability while indirectly sensing circulating nutrients through growth factor signaling pathways. Cellular stresses that restrict growth also impinge on mTORC1 activity. mTORC2 is less well understood and appears only to sense growth factors. As an integrator of diverse growth regulatory signals, mTOR evolved to be a central signaling hub for controlling cellular metabolism and energy homoeostasis, and defects in mTOR signaling are important in the pathologies of cancer, diabetes, and aging. Here we discuss mechanisms by which each mTOR complex might regulate cell survival in response to metabolic and other stresses.

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Year:  2012        PMID: 23124837      PMCID: PMC3504431          DOI: 10.1101/cshperspect.a008771

Source DB:  PubMed          Journal:  Cold Spring Harb Perspect Biol        ISSN: 1943-0264            Impact factor:   10.005


  131 in total

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5.  Mechanism of activation of protein kinase B by insulin and IGF-1.

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6.  AMPK directly activates mTORC2 to promote cell survival during acute energetic stress.

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