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IL-6 regulates autophagy and chemotherapy resistance by promoting BECN1 phosphorylation.

Fuqing HuDa SongYumeng YanChangsheng HuangChentao ShenJingqin LanYaqi ChenAnyi LiuQi WuLi SunFeng XuFayong HuLisheng ChenXuelai LuoYongdong FengSheng-You HuangJunbo HuGuihua Wang
Published in: Nature communications (2021)
Extracellular cytokines are enriched in the tumor microenvironment and regulate various important properties of cancers, including autophagy. However, the precise molecular mechanisms underlying the link between autophagy and extracellular cytokines remain to be elucidated. In the present study, we demonstrate that IL-6 activates autophagy through the IL-6/JAK2/BECN1 pathway and promotes chemotherapy resistance in colorectal cancer (CRC). Mechanistically, IL-6 triggers the interaction between JAK2 and BECN1, where JAK2 phosphorylates BECN1 at Y333. We demonstrate that BECN1 Y333 phosphorylation is crucial for BECN1 activation and IL-6-induced autophagy by regulating PI3KC3 complex formation. Furthermore, we investigate BECN1 Y333 phosphorylation as a predictive marker for poor CRC prognosis and chemotherapy resistance. Combination treatment with autophagy inhibitors or pharmacological agents targeting the IL-6/JAK2/BECN1 signaling pathway may represent a potential strategy for CRC cancer therapy.
Keyphrases
  • signaling pathway
  • cell death
  • endoplasmic reticulum stress
  • oxidative stress
  • cancer therapy
  • pi k akt
  • epithelial mesenchymal transition
  • diabetic rats
  • high glucose
  • chemotherapy induced