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dc.contributor.authorHung, Chien-Min
dc.contributor.authorGarcia-Haro, Luisa
dc.contributor.authorSparks, Cynthia A.
dc.contributor.authorGuertin, David A.
dc.date2022-08-11T08:08:56.000
dc.date.accessioned2022-08-23T16:12:58Z
dc.date.available2022-08-23T16:12:58Z
dc.date.issued2012-12-01
dc.date.submitted2017-09-13
dc.identifier.citation<p>Cold Spring Harb Perspect Biol. 2012 Dec 1;4(12). pii: a008771. doi: 10.1101/cshperspect.a008771. <a href="https://doi.org/10.1101/cshperspect.a008771">Link to article on publisher's site</a></p>
dc.identifier.issn1943-0264 (Linking)
dc.identifier.doi10.1101/cshperspect.a008771
dc.identifier.pmid23124837
dc.identifier.urihttp://hdl.handle.net/20.500.14038/33509
dc.description.abstractThe 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.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=23124837&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504431/
dc.subjectBiochemistry
dc.subjectCellular and Molecular Physiology
dc.titlemTOR-dependent cell survival mechanisms
dc.typeJournal Article
dc.source.journaltitleCold Spring Harbor perspectives in biology
dc.source.volume4
dc.source.issue12
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/2034
dc.identifier.contextkey10740193
html.description.abstract<p>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.</p>
dc.identifier.submissionpathgsbs_sp/2034
dc.contributor.departmentProgram in Molecular Medicine
dc.contributor.studentChien-Min Hung


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