<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhou J</submitter><funding>Changzhou Health Commission</funding><pagination>8727924</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8531794</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>2021</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The CXC chemokines belong to a unique family of cytokines that participates in the progression and development of many malignant tumors. Evidence for the relationship between chemokine (C-X-C motif) receptor 2 (CXCR2) C1208T polymorphism and susceptibility to cancer remains inconsistent.&lt;h4>Methods&lt;/h4>Odds ratios (ORs), 95% confidence intervals (CIs), and combined analysis were used to investigate the effect of CXCR2 variation on cancer risk. Gene Set Enrichment Analysis (GSEA) and enzyme-linked immunosorbent assay (ELISA) were also used to evaluate the expression of CXCR2 in prostate cancer (PCA).&lt;h4>Results&lt;/h4>Across 11 case-control studies, 4,909 cases and 5,884 controls were involved in the current analysis. Individuals with a TT genotype were associated with incre</pubmed_abstract><journal>Journal of immunology research</journal><pubmed_title>Impacts of Chemokine (C-X-C Motif) Receptor 2 C1208T Polymorphism on Cancer Susceptibility.</pubmed_title><pmcid>PMC8531794</pmcid><funding_grant_id>WZ201917</funding_grant_id><pubmed_authors>Tang BW</pubmed_authors><pubmed_authors>Chen XP</pubmed_authors><pubmed_authors>Su QX</pubmed_authors><pubmed_authors>Shi XK</pubmed_authors><pubmed_authors>Zhao CP</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Zhou J</pubmed_authors><pubmed_authors>Wu H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Impacts of Chemokine (C-X-C Motif) Receptor 2 C1208T Polymorphism on Cancer Susceptibility.</name><description>&lt;h4>Background&lt;/h4>The CXC chemokines belong to a unique family of cytokines that participates in the progression and development of many malignant tumors. Evidence for the relationship between chemokine (C-X-C motif) receptor 2 (CXCR2) C1208T polymorphism and susceptibility to cancer remains inconsistent.&lt;h4>Methods&lt;/h4>Odds ratios (ORs), 95% confidence intervals (CIs), and combined analysis were used to investigate the effect of CXCR2 variation on cancer risk. Gene Set Enrichment Analysis (GSEA) and enzyme-linked immunosorbent assay (ELISA) were also used to evaluate the expression of CXCR2 in prostate cancer (PCA).&lt;h4>Results&lt;/h4>Across 11 case-control studies, 4,909 cases and 5,884 controls were involved in the current analysis. Individuals with a TT genotype were associated with incre</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2026-03-27T16:15:16.978Z</modification><creation>2025-05-18T10:37:48.742Z</creation></dates><accession>S-EPMC8531794</accession><cross_references><pubmed>34692853</pubmed><doi>10.1155/2021/8727924</doi></cross_references></HashMap>