Abrogation of USP7 is an alternative strategy to downregulate PD-L1 and sensitize gastric cancer cells to T cells killing.
Acta Pharm Sin B
; 11(3): 694-707, 2021 Mar.
Article
in En
| MEDLINE
| ID: mdl-33777676
BCA, bicinchoninic acid; CHX, cycloheximide; CSN5, COP9 signalosome 5; Cancer biology; DUB, deubiquitinating enzymes; EBNA1, EpsteinBarr nuclear antigen 1; Epigenetics; FDA, U.S. Food and Drug Administration; FOXO4, forkhead box O4; GC, gastric cancer; GEPIA, Gene-Expression Profiling Interactive Analysis; Gastric cancer; H2O2, hydrogen peroxidase; HAUSP, herpes virus-associated ubiquitin-specific protease; HDN, well differentiated matched adjacent normal tissues; HDT, well differentiated tumor tissues; ICP0, infected cell protein 0; IL-2, interleukin 2; Immunosuppression; Immunotherapy; MDM2, murine double minute-2; PBMC, peripheral blood mononuclear cells; PBS, phosphate buffer saline; PD-1, programmed cell death protein 1; PD-L1; PD-L1, programmed death ligand-1; PDN, poor differentiated matched adjacent normal tissues; PDT, poor differentiated tumor tissues; PTMs, post-translational modifications; RIPA, radioimmunoprecipitation; TCGA, the Cancer Genome Atlas; TCR, T cell receptor; TILs, tumor-infiltrating T cells; USP18, ubiquitin specific peptidase 18; USP22, ubiquitin specific peptidase 22; USP38, ubiquitin specific peptidase 38; USP7; USP7, ubiquitin-specific processing protease 7; USP9X, ubiquitin specific peptidase 9 X-linked; Ubiquitination; WB, Western blotting; irAEs, immune-related adverse effects; qRT-PCR, quantitative real time polymerase chain reaction
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En
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Acta Pharm Sin B
Year:
2021
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Article
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