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Cited 6 time in webofscience Cited 7 time in scopus
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CXCR3 expression as a prognostic factor in gastric cancer: a meta-analysis

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dc.contributor.authorKoh, Hyun Min-
dc.contributor.authorHyun, Chang Lim-
dc.contributor.authorJang, Bo Gun-
dc.contributor.authorLee, Hyun Ju-
dc.date.accessioned2024-12-02T23:00:52Z-
dc.date.available2024-12-02T23:00:52Z-
dc.date.issued2021-03-
dc.identifier.issn2218-676X-
dc.identifier.issn2219-6803-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/72764-
dc.description.abstractBackground: CXC chemokine receptor 3 (CXCR3) plays a critical role in tumorigenesis, and CXCR3 expression is associated with prognosis in many cancers. Recently, CXCR3 expression is recognized as a potential prognostic factor for patients with gastric cancer. In this study, we analyzed the prognostic significance of CXCR3 expression in gastric cancer. Methods: We conducted a meta-analysis after selecting eligible studies through a literature search. We calculated pooled results to assess the associations between CXCR3 expression and overall survival (OS) and clinicopathological factors for gastric cancer. Results: The pooled hazard ratio (HR) with 95% confidence interval (CI) between high expression of CXCR3 and OS was 0.46 (95% CI 0.30-0.71, P<0.001), suggesting that high expression of CXCR3 was associated with a favorable OS. High expression of CXCR3 was significantly correlated with younger age [odds ratio (OR) 0.67, 95% CI: 0.49-0.91, P=0.011], lower tumor grade (OR 0.46, 95% CI: 0.29-0.73, P=0.001), absence of lymph node metastasis (OR 0.47, 95% CI: 0.31-0.71, P<0.001), and lower Tumor-Node-Metastasis stage (OR 0.51, 95% CI: 0.35-0.74, P<0.001). Conclusions: High expression of CXCR3 was associated with better survival and may be a potential prognostic factor for patients with gastric cancer patients.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherAME PUBLISHING COMPANY-
dc.titleCXCR3 expression as a prognostic factor in gastric cancer: a meta-analysis-
dc.typeArticle-
dc.publisher.location중국-
dc.identifier.doi10.21037/tcr-20-2862-
dc.identifier.scopusid2-s2.0-85103594326-
dc.identifier.wosid000635021300025-
dc.identifier.bibliographicCitationTRANSLATIONAL CANCER RESEARCH, v.10, no.3, pp 1449 - 1456-
dc.citation.titleTRANSLATIONAL CANCER RESEARCH-
dc.citation.volume10-
dc.citation.number3-
dc.citation.startPage1449-
dc.citation.endPage1456-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.subject.keywordPlusCHEMOKINE RECEPTOR CXCR3-
dc.subject.keywordPlusFAVORABLE PROGNOSIS-
dc.subject.keywordPlusOVEREXPRESSION-
dc.subject.keywordPlusPROMOTES-
dc.subject.keywordPlusRECRUITMENT-
dc.subject.keywordPlusCARCINOMA-
dc.subject.keywordAuthorCXC chemokine receptor 3 (CXCR3)-
dc.subject.keywordAuthorgastric cancer-
dc.subject.keywordAuthormeta-analysis-
dc.subject.keywordAuthorprognosis-
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