<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kamai T</submitter><funding>Japanese Science Progress Society KAKENHI Grants</funding><pagination>2009-2021</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8195893</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>70(7)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Adenosine and its adenosine 2A receptors (A2AR) mediate the immunosuppressive mechanism by which tumors escape immunosurveillance and impede anti-tumor immunity within the tumor microenvironment. However, we do not know whether the adenosine pathway (CD39/CD73/A2AR) plays a role in renal cell carcinoma (RCC). Therefore, we studied the role of immunosuppression in RCC by assessing the adenosine pathway in patients with RCC treated with anti-vascular endothelial growth factor (anti-VEGF) agents or immune checkpoints inhibitors (ICIs) or both.&lt;h4>Methods&lt;/h4>In 60 patients with metastatic RCC, we examined the expression of CD39, CD73, A2AR, and programmed cell death 1 ligand 1 (PD-L1) immunohistochemically in surgically resected tumor tissues and studied the clinicopatholog</pubmed_abstract><journal>Cancer immunology, immunotherapy : CII</journal><pubmed_title>Increased expression of adenosine 2A receptors in metastatic renal cell carcinoma is associated with poorer response to anti-vascular endothelial growth factor agents and anti-PD-1/Anti-CTLA4 antibodies and shorter survival.</pubmed_title><pmcid>PMC8195893</pmcid><funding_grant_id>17K11156, 20K09546</funding_grant_id><pubmed_authors>Kamai T</pubmed_authors><pubmed_authors>Tsuzuki T</pubmed_authors><pubmed_authors>Kijima T</pubmed_authors><pubmed_authors>Arai K</pubmed_authors><pubmed_authors>Yoshida KI</pubmed_authors><pubmed_authors>Nukui A</pubmed_authors><pubmed_authors>Abe H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Increased expression of adenosine 2A receptors in metastatic renal cell carcinoma is associated with poorer response to anti-vascular endothelial growth factor agents and anti-PD-1/Anti-CTLA4 antibodies and shorter survival.</name><description>&lt;h4>Background&lt;/h4>Adenosine and its adenosine 2A receptors (A2AR) mediate the immunosuppressive mechanism by which tumors escape immunosurveillance and impede anti-tumor immunity within the tumor microenvironment. However, we do not know whether the adenosine pathway (CD39/CD73/A2AR) plays a role in renal cell carcinoma (RCC). Therefore, we studied the role of immunosuppression in RCC by assessing the adenosine pathway in patients with RCC treated with anti-vascular endothelial growth factor (anti-VEGF) agents or immune checkpoints inhibitors (ICIs) or both.&lt;h4>Methods&lt;/h4>In 60 patients with metastatic RCC, we examined the expression of CD39, CD73, A2AR, and programmed cell death 1 ligand 1 (PD-L1) immunohistochemically in surgically resected tumor tissues and studied the clinicopatholog</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jul</publication><modification>2025-04-26T00:32:53.771Z</modification><creation>2022-02-10T16:47:41.973Z</creation></dates><accession>S-EPMC8195893</accession><cross_references><pubmed>33416945</pubmed><doi>10.1007/s00262-020-02843-x</doi></cross_references></HashMap>