<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(14)</volume><submitter>Shao YY</submitter><pubmed_abstract>The anti-programmed death-ligand 1 (PD-L1) antibody is a standard therapy for advanced hepatocellular carcinoma (HCC). Tumor expression of PD-L1 can be induced upon stimulus. Because cyclin-dependent kinase 9 (CDK9) inhibition reduces the expression of inducible proteins, we explored the influence of CDK9 inhibition on PD-L1 expression in HCC cells. We found that PD-L1 expression was low in HCC cells; however, IFN-γ treatment increased this expression. CDK9 inhibitors AZD4573 and atuveciclib reduced the IFN-γ induced PD-L1 expression in a dose-dependent manner. CDK9 knockdown yielded similar results, but CDK9 overexpression reversed the influence of the CDK9 inhibitors. In the orthotopic mouse model, mice treated with a CDK9 inhibitor and an anti-PD-L1 antibody had significantly smaller tumors and exhibited longer survival than mice treated with either agent. In conclusion, CDK9 inhibition could reduce the expression of PD-L1 in HCC cells. Using both CDK9 inhibitors and anti-PD-L1 antibodies is more effective than using either agent alone.</pubmed_abstract><journal>Heliyon</journal><pagination>e34289</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11296019</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Cyclin dependent kinase 9 inhibition reduced programmed death-ligand 1 expression and improved treatment efficacy in hepatocellular carcinoma.</pubmed_title><pmcid>PMC11296019</pmcid><pubmed_authors>Hsu HW</pubmed_authors><pubmed_authors>Wo RR</pubmed_authors><pubmed_authors>Hsieh MS</pubmed_authors><pubmed_authors>Shao YY</pubmed_authors><pubmed_authors>Hsu CH</pubmed_authors><pubmed_authors>Lee YH</pubmed_authors><pubmed_authors>Wang HY</pubmed_authors><pubmed_authors>Cheng AL</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cyclin dependent kinase 9 inhibition reduced programmed death-ligand 1 expression and improved treatment efficacy in hepatocellular carcinoma.</name><description>The anti-programmed death-ligand 1 (PD-L1) antibody is a standard therapy for advanced hepatocellular carcinoma (HCC). Tumor expression of PD-L1 can be induced upon stimulus. Because cyclin-dependent kinase 9 (CDK9) inhibition reduces the expression of inducible proteins, we explored the influence of CDK9 inhibition on PD-L1 expression in HCC cells. We found that PD-L1 expression was low in HCC cells; however, IFN-γ treatment increased this expression. CDK9 inhibitors AZD4573 and atuveciclib reduced the IFN-γ induced PD-L1 expression in a dose-dependent manner. CDK9 knockdown yielded similar results, but CDK9 overexpression reversed the influence of the CDK9 inhibitors. In the orthotopic mouse model, mice treated with a CDK9 inhibitor and an anti-PD-L1 antibody had significantly smaller tumors and exhibited longer survival than mice treated with either agent. In conclusion, CDK9 inhibition could reduce the expression of PD-L1 in HCC cells. Using both CDK9 inhibitors and anti-PD-L1 antibodies is more effective than using either agent alone.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2026-06-02T22:10:26.881Z</modification><creation>2025-02-19T02:27:47.983Z</creation></dates><accession>S-EPMC11296019</accession><cross_references><pubmed>39100490</pubmed><doi>10.1016/j.heliyon.2024.e34289</doi></cross_references></HashMap>