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10.1073/pnas.1705338114

http://scihub22266oqcxt.onion/10.1073/pnas.1705338114
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C5604011!5604011!28851829
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suck abstract from ncbi


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pmid28851829      Proc+Natl+Acad+Sci+U+S+A 2017 ; 114 (37): 9948-53
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  • Glucocorticoids promote Von Hippel Lindau degradation and Hif-1? stabilization #MMPMID28851829
  • Vettori A; Greenald D; Wilson GK; Peron M; Facchinello N; Markham E; Sinnakaruppan M; Matthews LC; McKeating JA; Argenton F; van Eeden FJM
  • Proc Natl Acad Sci U S A 2017[Sep]; 114 (37): 9948-53 PMID28851829show ga
  • An in vivo chemical screen in zebrafish identified glucocorticoids (GCs) as activators of hypoxia-inducible factor transcriptional responses in the liver. This cross-talk is conserved in human liver and requires glucocorticoid receptor signaling but not DNA binding. In human liver cells, GCs down-regulate Von Hippel Lindau expression at a posttranscriptional level most likely through c-src?mediated proteasomal degradation. Since the liver is an important regulator of blood glucose and hypoxia-inducible factors regulate gluconeogenesis/glycogen synthesis, cross-talk between these transcriptional regulators may be essential to control glucose metabolism in the liver. This identified, conserved, noncanonical pathway may have wider physiological significance in health and disease.
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