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CRIP1 fosters MDSC trafficking and resets tumour microenvironment via facilitating NF-κB/p65 nuclear translocation in pancreatic ductal adenocarcinoma.

Xiaomeng LiuRong TangJin XuZhen TanChen LiangQingcai MengYubin LeiJie HuaYiyin ZhangJiang LiuBo ZhangWei WangXianjun YuXianjun Yu
Published in: Gut (2023)
The CRIP1/NF-κB/CXCL axis is critical for triggering immune evasion and TIME formation in PDAC. Blockade of this signalling pathway prevents MDSC trafficking and thereby sensitises PDAC to immunotherapy.
Keyphrases
  • signaling pathway
  • lps induced
  • pi k akt
  • nuclear factor
  • oxidative stress
  • stem cells
  • inflammatory response
  • mouse model
  • toll like receptor
  • cell proliferation