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Smad4 May Help to Identify a Subset of Colorectal Cancer Patients with Early Recurrence after Curative Therapy

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dc.contributor.authorAhn, Byung Kyu-
dc.contributor.authorJang, Si-Hyong-
dc.contributor.authorPaik, Seung Sam-
dc.contributor.authorLee, Kang Hong-
dc.date.accessioned2022-07-16T18:24:25Z-
dc.date.available2022-07-16T18:24:25Z-
dc.date.created2021-05-12-
dc.date.issued2011-11-
dc.identifier.issn0172-6390-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/167253-
dc.description.abstractBackground/Aims: Loss of Smad4 function is associated with the acquisition of advanced colorectal cancer phenotypes. We investigated the role of Smad4 as a prognostic marker after curative therapy. Methodology: Four hundred and twenty nine consecutive colorectal cancers were analyzed by tissue microarray-based immunohistochemical assay. Results: Smad4 protein was expressed in 61.5% (24/39), 53.1% (77/145), 41.3% (78/189) and 34.8% (16/46) of stage I, II, III and IV cancers, respectively. Lymphovascular invasion and lymph node metastasis were strongly correlated with the loss of Smad4 expression (p<0.0001 and p=0.002, respectively). Disease-free survival did not differ between Smad4-positive and Smad4-negative cancers. In stage Ill disease, time to recurrence after curative therapy was shorter in the Smad4-negative than in the Smad4-positive cancers (20.1 +/- 15.1 vs. 34.6 +/- 34.1 months, p=0.035). Conclusions: Smad4 protein is of no value in predicting recurrence after curative therapy in colorectal cancer, but it may be helpful in identifying a subset of patients with early recurrence after curative therapy.-
dc.language영어-
dc.language.isoen-
dc.publisherH G E UPDATE MEDICAL PUBLISHING S A-
dc.titleSmad4 May Help to Identify a Subset of Colorectal Cancer Patients with Early Recurrence after Curative Therapy-
dc.typeArticle-
dc.contributor.affiliatedAuthorAhn, Byung Kyu-
dc.contributor.affiliatedAuthorPaik, Seung Sam-
dc.contributor.affiliatedAuthorLee, Kang Hong-
dc.identifier.doi10.5754/hge11186-
dc.identifier.scopusid2-s2.0-84863251477-
dc.identifier.wosid000300532700018-
dc.identifier.bibliographicCitationHEPATO-GASTROENTEROLOGY, v.58, no.112, pp.1933 - 1936-
dc.relation.isPartOfHEPATO-GASTROENTEROLOGY-
dc.citation.titleHEPATO-GASTROENTEROLOGY-
dc.citation.volume58-
dc.citation.number112-
dc.citation.startPage1933-
dc.citation.endPage1936-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaGastroenterology & Hepatology-
dc.relation.journalResearchAreaSurgery-
dc.relation.journalWebOfScienceCategoryGastroenterology & Hepatology-
dc.relation.journalWebOfScienceCategorySurgery-
dc.subject.keywordPlus18Q ALLELIC LOSS-
dc.subject.keywordPlusCHROMOSOME 18Q-
dc.subject.keywordPlusCOLON-CANCER-
dc.subject.keywordPlusGENE-
dc.subject.keywordPlusPROGNOSIS-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusMUTATIONS-
dc.subject.keywordPlusSURVIVAL-
dc.subject.keywordAuthorSmad4-
dc.subject.keywordAuthorColorectal cancer-
dc.subject.keywordAuthorCarcinogenesis-
dc.subject.keywordAuthorPrognosis-
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