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10.12688/f1000research.9207.1

http://scihub22266oqcxt.onion/10.12688/f1000research.9207.1
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C5007757!5007757!27635236
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suck abstract from ncbi

pmid27635236      F1000Res 2016 ; 5 (ä): ä
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  • mTOR inhibitors in cancer therapy #MMPMID27635236
  • Xie J; Wang X; Proud CG
  • F1000Res 2016[]; 5 (ä): ä PMID27635236show ga
  • The mammalian target of rapamycin, mTOR, plays key roles in cell growth and proliferation, acting at the catalytic subunit of two protein kinase complexes: mTOR complexes 1 and 2 (mTORC1/2). mTORC1 signaling is switched on by several oncogenic signaling pathways and is accordingly hyperactive in the majority of cancers. Inhibiting mTORC1 signaling has therefore attracted great attention as an anti-cancer therapy. However, progress in using inhibitors of mTOR signaling as therapeutic agents in oncology has been limited by a number of factors, including the fact that the classic mTOR inhibitor, rapamycin, inhibits only some of the effects of mTOR; the existence of several feedback loops; and the crucial importance of mTOR in normal physiology.
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