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10.18632/oncotarget.13321

http://scihub22266oqcxt.onion/10.18632/oncotarget.13321
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C5356702!5356702!27863375
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suck abstract from ncbi


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pmid27863375      Oncotarget 2016 ; 7 (51): 84839-50
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  • H2O2 treatment or serum deprivation induces autophagy and apoptosis in naked mole-rat skin fibroblasts by inhibiting the PI3K/Akt signaling pathway #MMPMID27863375
  • Zhao S; Li L; Wang S; Yu C; Xiao B; Lin L; Cong W; Cheng J; Yang W; Sun W; Cui S
  • Oncotarget 2016[Dec]; 7 (51): 84839-50 PMID27863375show ga
  • Naked mole-rats (NMR; Heterocephalus glaber) display extreme longevity and resistance to cancer. Here, we examined whether autophagy contributes to the longevity of NMRs by assessing the effects of the PI3K/Akt pathway inhibitor LY294002 and the autophagy inhibitor chloroquine (CQ) on autophagy and apoptosis in NMR skin fibroblasts. Serum starvation, H2O2 treatment, and LY294002 treatment all increased the LC3-II/LC3-I ratio and numbers of double-membraned autophagosomes and autophagic vacuoles, and decreased levels of p70S6K, p-AktSer473, and p-AktThr308. By contrast, CQ treatment decreased p70S6K, AktSer473, and AktThr308 levels. The Bax/Bcl-2 ratio increased after 12 h of exposure to LY294002 or CQ. These data show that inhibiting the Akt pathway promotes autophagy and apoptosis in NMR skin fibroblasts. Furthermore, LY294002 or CQ treatment decreased caspase-3, p53, and HIF1-? levels, suggesting that serum starvation or H2O2 treatment increase autophagy and apoptosis in NMR skin fibroblasts by inhibiting the PI3K/Akt pathway. CQ-induced inhibition of late autophagy stages also prevented Akt activation and induced apoptosis. Finally, the HIF-1? and p53 pathways were involved in serum starvation- or H2O2-induced autophagy in NMR skin fibroblasts.
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