<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(97)</volume><submitter>Ahlmanner F</submitter><pubmed_abstract>Increasing knowledge of the function and regulation of tumor-infiltrating lymphocytes has led to new insights in cancer immunotherapy. Regulatory T cells (Treg) accumulate in colon tumors, and we recently showed that CD39&lt;sup>+&lt;/sup> Treg from cancer patients inhibit transendothelial migration of conventional T cells. CD39 mediates the hydrolysis of ATP to immunosuppressive adenosine and adds to the immunosuppressive effects of Treg. Here, we further investigated the regulatory features of intratumoral CD39&lt;sup>+&lt;/sup> Treg in colon cancer. Using flow cytometry analyses of cells from 46 colon cancer patients, we confirm the accumulation of CD39&lt;sup>+&lt;/sup> Treg in the tumor tissue compared to unaffected colon tissue, and also show that tumor-infiltrating Treg express more CD39 and Foxp3 on</pubmed_abstract><journal>Oncotarget</journal><pagination>36993-37007</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6319332</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>CD39&lt;sup>+&lt;/sup> regulatory T cells accumulate in colon adenocarcinomas and display markers of increased suppressive function.</pubmed_title><pmcid>PMC6319332</pmcid><pubmed_authors>Borjesson L</pubmed_authors><pubmed_authors>Gustavsson B</pubmed_authors><pubmed_authors>Akeus P</pubmed_authors><pubmed_authors>Ahlmanner F</pubmed_authors><pubmed_authors>Quiding-Jarbrink M</pubmed_authors><pubmed_authors>Sundstrom P</pubmed_authors><pubmed_authors>Lindskog EB</pubmed_authors><pubmed_authors>Eklof J</pubmed_authors><pubmed_authors>Raghavan S</pubmed_authors></additional><is_claimable>false</is_claimable><name>CD39&lt;sup>+&lt;/sup> regulatory T cells accumulate in colon adenocarcinomas and display markers of increased suppressive function.</name><description>Increasing knowledge of the function and regulation of tumor-infiltrating lymphocytes has led to new insights in cancer immunotherapy. Regulatory T cells (Treg) accumulate in colon tumors, and we recently showed that CD39&lt;sup>+&lt;/sup> Treg from cancer patients inhibit transendothelial migration of conventional T cells. CD39 mediates the hydrolysis of ATP to immunosuppressive adenosine and adds to the immunosuppressive effects of Treg. Here, we further investigated the regulatory features of intratumoral CD39&lt;sup>+&lt;/sup> Treg in colon cancer. Using flow cytometry analyses of cells from 46 colon cancer patients, we confirm the accumulation of CD39&lt;sup>+&lt;/sup> Treg in the tumor tissue compared to unaffected colon tissue, and also show that tumor-infiltrating Treg express more CD39 and Foxp3 on</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Dec</publication><modification>2025-04-18T14:30:00.385Z</modification><creation>2019-03-26T22:37:34Z</creation></dates><accession>S-EPMC6319332</accession><cross_references><pubmed>30651930</pubmed><doi>10.18632/oncotarget.26435</doi></cross_references></HashMap>