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10.1101/gad.290940.116

http://scihub22266oqcxt.onion/10.1101/gad.290940.116
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C5287109!5287109!28096186
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suck abstract from ncbi


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pmid28096186      Genes+Dev 2017 ; 31 (1): 18-33
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  • Translation reprogramming is an evolutionarily conserved driver of phenotypic plasticity and therapeutic resistance in melanoma #MMPMID28096186
  • Falletta P; Sanchez-del-Campo L; Chauhan J; Effern M; Kenyon A; Kershaw CJ; Siddaway R; Lisle R; Freter R; Daniels MJ; Lu X; Tüting T; Middleton M; Buffa FM; Willis AE; Pavitt G; Ronai ZA; Sauka-Spengler T; Hölzel M; Goding CR
  • Genes Dev 2017[Jan]; 31 (1): 18-33 PMID28096186show ga
  • In this study, Falletta et al. show that microenvironmental cues, including inflammation-mediated resistance to adoptive T-cell immunotherapy, transcriptionally repress MITF via ATF4 in response to inhibition of translation initiation factor eIF2B. Their results suggest that translation reprogramming, an evolutionarily conserved starvation response, has been hijacked by microenvironmental stress signals in melanoma to drive phenotypic plasticity and invasion and determine therapeutic outcome.
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