<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(9)</volume><submitter>Feng W</submitter><pubmed_abstract>Ovarian cancer is insensitive to immunotherapy and has a high mortality rate. CDK4/6 inhibitors (CDK4/6i) regulate the tumor microenvironment and play an antitumor role. Our previous research demonstrated that lymphocyte aggregation (tertiary lymphoid structures, TLSs) was observed after CDK4/6i treatment. This may explain the synergistic action of CDK4/6i with the anti-PD1 antibody. However, the key mechanism by which CDK4/6i promotes TLS formation has not been elucidated. We examine the link between TLS and prognosis. Animal models and high-throughput sequencing were used to explore the potential mechanism by which CDK4/6i promotes TLS formation. Our results showed the presence of TLSs was associated with a favorable prognosis for ovarian cancer. CDK4/6i promoted TLS formation and enhanced the immunotherapeutic effect of the anti-PD1 antibody. The potential mechanism of CDK4/6i affecting the formation of TLS may be through modulating SCD1 and its regulatory molecules ATF3 and CCL4. Our findings provide a theoretical basis for the application of CDK4/6i in ovarian cancer.</pubmed_abstract><journal>Heliyon</journal><pagination>e19760</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10559077</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>CDK4/6i enhances the antitumor effect of PD1 antibody by promoting TLS formation in ovarian cancer.</pubmed_title><pmcid>PMC10559077</pmcid><pubmed_authors>Yang H</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Zhao M</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Chen L</pubmed_authors><pubmed_authors>Liao W</pubmed_authors><pubmed_authors>Feng W</pubmed_authors><pubmed_authors>Jiang D</pubmed_authors><pubmed_authors>Shen Y</pubmed_authors><pubmed_authors>Xu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>CDK4/6i enhances the antitumor effect of PD1 antibody by promoting TLS formation in ovarian cancer.</name><description>Ovarian cancer is insensitive to immunotherapy and has a high mortality rate. CDK4/6 inhibitors (CDK4/6i) regulate the tumor microenvironment and play an antitumor role. Our previous research demonstrated that lymphocyte aggregation (tertiary lymphoid structures, TLSs) was observed after CDK4/6i treatment. This may explain the synergistic action of CDK4/6i with the anti-PD1 antibody. However, the key mechanism by which CDK4/6i promotes TLS formation has not been elucidated. We examine the link between TLS and prognosis. Animal models and high-throughput sequencing were used to explore the potential mechanism by which CDK4/6i promotes TLS formation. Our results showed the presence of TLSs was associated with a favorable prognosis for ovarian cancer. CDK4/6i promoted TLS formation and enhanced the immunotherapeutic effect of the anti-PD1 antibody. The potential mechanism of CDK4/6i affecting the formation of TLS may be through modulating SCD1 and its regulatory molecules ATF3 and CCL4. Our findings provide a theoretical basis for the application of CDK4/6i in ovarian cancer.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Sep</publication><modification>2024-11-20T18:27:32.136Z</modification><creation>2024-11-20T18:27:32.136Z</creation></dates><accession>S-EPMC10559077</accession><cross_references><pubmed>37809574</pubmed><doi>10.1016/j.heliyon.2023.e19760</doi></cross_references></HashMap>