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10.1016/j.tem.2014.04.002

http://scihub22266oqcxt.onion/10.1016/j.tem.2014.04.002
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C4077930!4077930!24856037
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suck abstract from ncbi


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pmid24856037      Trends+Endocrinol+Metab 2014 ; 25 (7): 364-73
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  • mTORC2 in the center of cancer metabolic reprogramming #MMPMID24856037
  • Masui K; Cavenee WK; Mischel PS
  • Trends Endocrinol Metab 2014[Jul]; 25 (7): 364-73 PMID24856037show ga
  • Metabolic reprogramming is a central hallmark of cancer, enabling tumor cells to obtain the macromolecular precursors and energy needed for rapid tumor growth. Understanding how oncogenes coordinate altered signaling with metabolic reprogramming and global transcription may yield new insights into tumor pathogenesis, and provide a new landscape of promising drug targets, while yielding important clues into mechanisms of resistance to the signal transduction inhibitors currently in use. Here we review the recently identified central regulatory role for mTORC2, a downstream effector of many cancer-causing mutations, in metabolic reprogramming and cancer drug resistance. We consider the impact of mTORC2-related metabolism on epigenetics and therapeutics, with a particular focus on the intractable malignant brain tumor, glioblastoma (GBM).
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