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Prognostic significance of IFITM1 expression and correlation with microvessel density and epithelial-mesenchymal transition signature in lung adenocarcinoma

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dc.contributor.authorKoh, Young Wha-
dc.contributor.authorHan, Jae-Ho-
dc.contributor.authorJeong, Dongjun-
dc.contributor.authorKim, Chang-Jin-
dc.date.accessioned2021-08-11T09:43:41Z-
dc.date.available2021-08-11T09:43:41Z-
dc.date.issued2019-07-
dc.identifier.issn0344-0338-
dc.identifier.urihttps://scholarworks.bwise.kr/sch/handle/2021.sw.sch/4429-
dc.description.abstractWe evaluated the relationship between interferon-induced transmembrane protein 1 (IFITM1) expression, epithelial-mesenchymal transition (EMT) signature and angiogenesis in lung adenocarcinoma. Additionally, we examined prognostic significance of IFITM1 according to pTNM stage to confirm that IFITM1 can serve as a complement to the pTNM stage. A total of 141 lung adenocarcinoma specimens were evaluated retrospectively by immunohistochemical staining for IFITM1, EMT markers (e-cadherin, beta-catenin, and vimentin), and CD31 to measure microvessel density. IFITM1 was expressed in 46.8% of the specimens. IFITM1 expression was significantly correlated with increased microvessel density (P = 0.048). However, IFITM1 expression was not associated with three EMT markers. In a multivariate analysis, IFITM1 was an independent prognostic factor for overall survival in a multivariate analysis (hazard ratio: 2.59, P = 0.01). Online database with data from 720 lung adenocarcinoma patients also revealed a negative prognostic significance of IFITM1 (P < 0.001). Furthermore, high IFITM1 expression was significantly correlated with decreased OS rates in each pTNM stage. IFITM1 is significantly correlated with angiogenesis and it may be used as a useful additional prognostic marker to aid pTNM classification.-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier BV-
dc.titlePrognostic significance of IFITM1 expression and correlation with microvessel density and epithelial-mesenchymal transition signature in lung adenocarcinoma-
dc.typeArticle-
dc.publisher.location독일-
dc.identifier.doi10.1016/j.prp.2019.152444-
dc.identifier.scopusid2-s2.0-85065252299-
dc.identifier.wosid000474674200009-
dc.identifier.bibliographicCitationPathology Research and Practice, v.215, no.7-
dc.citation.titlePathology Research and Practice-
dc.citation.volume215-
dc.citation.number7-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPathology-
dc.relation.journalWebOfScienceCategoryPathology-
dc.subject.keywordPlusINDUCED TRANSMEMBRANE PROTEIN-1-
dc.subject.keywordPlusBREAST-CANCER CELLS-
dc.subject.keywordPlusTNM STAGE GROUPINGS-
dc.subject.keywordPlusMONOCLONAL-ANTIBODY-
dc.subject.keywordPlus8TH EDITION-
dc.subject.keywordPlusCLASSIFICATION-
dc.subject.keywordPlusPROLIFERATION-
dc.subject.keywordPlusAGGREGATION-
dc.subject.keywordPlusREVISION-
dc.subject.keywordAuthorLung adenocarcinoma-
dc.subject.keywordAuthorInterferon-induced transmembrane protein 1-
dc.subject.keywordAuthorMicrovessel-
dc.subject.keywordAuthorDensity-
dc.subject.keywordAuthorEpithelial-mesenchymal transition-
dc.subject.keywordAuthorPrognosis-
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