Abstract
MHC-I downregulation is correlated with immunotherapy resistance in PDAC, but efficient strategies to increase cell-surface MHC-I are still lacking. This study by Sang, Zhou, Chen, Yu, and colleagues identified inhibition of tumor-intrinsic RIPK2 as a pharmacologic target to block the degradation of MHC-I on tumor cells and improved PDAC responses to anti-PD-1 immunotherapy.
Original language | English |
---|---|
Pages (from-to) | 208-210 |
Number of pages | 3 |
Journal | Cancer discovery |
Volume | 14 |
Issue number | 2 |
DOIs | |
State | Published - 2024 |