<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hwang SH</submitter><funding>National research foundation (KR)</funding><funding>National research foundation</funding><pagination>137</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11566202</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Within the tumor microenvironment, altered lipid metabolism promotes cancer cell malignancy by activating oncogenic cascades; however, impact of lipid metabolism in CD4&lt;sup>+&lt;/sup> tumor-infiltrating lymphocytes (TILs) remains poorly understood. Here, we elucidated that role of stearoyl-CoA desaturase (SCD) increased by treatment with cancer-associated fibroblast (CAF) supernatant in CD4&lt;sup>+&lt;/sup> T cells on their subset differentiation and activity of CD8&lt;sup>+&lt;/sup> T cells.&lt;h4>Results&lt;/h4>In our study, we observed that CD4&lt;sup>+&lt;/sup> TILs had higher lipid droplet content than CD4&lt;sup>+&lt;/sup> splenic T cells. In tumor tissue, CAF-derived supernatant provided fatty acids to CD4&lt;sup>+&lt;/sup> TILs, which increased the expression of SCD and oleic acid (OA) content. Incre</pubmed_abstract><journal>Cell &amp; bioscience</journal><pubmed_title>Stearoyl-CoA desaturase in CD4&lt;sup>+&lt;/sup> T cells suppresses tumor growth through activation of the CXCR3/CXCL11 axis in CD8&lt;sup>+&lt;/sup> T cells.</pubmed_title><pmcid>PMC11566202</pmcid><funding_grant_id>RS-2023-00249667</funding_grant_id><funding_grant_id>2020R1A2C1010215</funding_grant_id><funding_grant_id>RS-2024-00351740</funding_grant_id><pubmed_authors>Yang Y</pubmed_authors><pubmed_authors>Hwang SH</pubmed_authors><pubmed_authors>Kim Y</pubmed_authors><pubmed_authors>Jung JH</pubmed_authors><pubmed_authors>Kim JW</pubmed_authors></additional><is_claimable>false</is_claimable><name>Stearoyl-CoA desaturase in CD4&lt;sup>+&lt;/sup> T cells suppresses tumor growth through activation of the CXCR3/CXCL11 axis in CD8&lt;sup>+&lt;/sup> T cells.</name><description>&lt;h4>Background&lt;/h4>Within the tumor microenvironment, altered lipid metabolism promotes cancer cell malignancy by activating oncogenic cascades; however, impact of lipid metabolism in CD4&lt;sup>+&lt;/sup> tumor-infiltrating lymphocytes (TILs) remains poorly understood. Here, we elucidated that role of stearoyl-CoA desaturase (SCD) increased by treatment with cancer-associated fibroblast (CAF) supernatant in CD4&lt;sup>+&lt;/sup> T cells on their subset differentiation and activity of CD8&lt;sup>+&lt;/sup> T cells.&lt;h4>Results&lt;/h4>In our study, we observed that CD4&lt;sup>+&lt;/sup> TILs had higher lipid droplet content than CD4&lt;sup>+&lt;/sup> splenic T cells. In tumor tissue, CAF-derived supernatant provided fatty acids to CD4&lt;sup>+&lt;/sup> TILs, which increased the expression of SCD and oleic acid (OA) content. Incre</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Nov</publication><modification>2026-07-16T22:37:25.546Z</modification><creation>2025-04-06T01:39:47.349Z</creation></dates><accession>S-EPMC11566202</accession><cross_references><pubmed>39543650</pubmed><doi>10.1186/s13578-024-01308-3</doi></cross_references></HashMap>