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Reduced Expression of DKK3 Is Associated With Adverse Clinical Outcomes of Uterine Cervical Squamous Cell Carcinoma

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dc.contributor.authorRyu, Seok-Woo-
dc.contributor.authorKim, Jae Hyung-
dc.contributor.authorKim, Mi Kyung-
dc.contributor.authorLee, Youn-Jeong-
dc.contributor.authorPark, Jun-Soo-
dc.contributor.authorPark, Hyoung-Moo-
dc.contributor.authorKim, Dong-Ho-
dc.contributor.authorLee, Sang-Hoon-
dc.contributor.authorLee, Eun-Ju-
dc.date.available2019-03-09T02:39:03Z-
dc.date.issued2013-01-
dc.identifier.issn1048-891X-
dc.identifier.issn1525-1438-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/14992-
dc.description.abstractObjective: The aim of this study was to assess the expression of DKK3 protein and its target, beta-catenin, in uterine cervical squamous cell carcinoma and to determine potential clinical correlations. Materials and Methods: Six carcinoma in-situ (CIS) tissues and 88 invasive cervical cancer tissues were included in the study. Twenty-two normal cervical tissues and one gastric cancer tissue were used as controls. The expression of DKK3 and beta-catenin proteins was evaluated by immunohistochemical analysis. Clinical and pathological parameters were obtained from medical records. Survival data were estimated using Kaplan-Meier estimates and compared with a log-rank test. Multivariate analysis was performed using the Cox regression method. Results: DICK3 was predominantly present in the cytoplasm. Beta-catenin was observed only on the cellular membrane of both normal and cancer cells in contrast to earlier reports, in which beta-catenin was localized to the cytoplasm and nucleus of cancer cells. The expressions of beta-catenin and DKK3 were not correlated. Three of 6 CIS (50%) and 57 of 88 invasive cancer specimens (64.8%) had lower DKK3 expression than normal controls. DKK3 expression was decreased in a stage-dependent manner (P = 0.021). The patients with low expression of DKK3 were older than those with high expression of DKK3 (P < 0.01). Moreover, the patients with low DKK3 expression had a significantly lower 5-year disease-free survival rate than those with high DKK3 expression (P = 0.026). A multivariate analysis showed that International Federation of Gynecology and Obstetrics clinical stage and parametrial involvement were independent prognostic factors. Conclusion: Decreased DKK3 expression was associated with advanced International Federation of Gynecology and Obstetrics clinical stages and was predictive of lower disease-free survival in patients with cervical squamous cell carcinoma. DKK3 may be implicated in cervical carcinogenesis through a beta-catenin independent mechanism.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherLIPPINCOTT WILLIAMS & WILKINS-
dc.titleReduced Expression of DKK3 Is Associated With Adverse Clinical Outcomes of Uterine Cervical Squamous Cell Carcinoma-
dc.typeArticle-
dc.identifier.doi10.1097/IGC.0b013e3182754feb-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, v.23, no.1, pp 134 - 140-
dc.description.isOpenAccessN-
dc.identifier.wosid000314005000019-
dc.identifier.scopusid2-s2.0-84872354688-
dc.citation.endPage140-
dc.citation.number1-
dc.citation.startPage134-
dc.citation.titleINTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER-
dc.citation.volume23-
dc.type.docTypeArticle-
dc.publisher.location미국-
dc.subject.keywordAuthorCervical cancer-
dc.subject.keywordAuthorDKK3-
dc.subject.keywordAuthorBeta-catenin-
dc.subject.keywordPlusBETA-CATENIN-
dc.subject.keywordPlusPROMOTER-HYPERMETHYLATION-
dc.subject.keywordPlusPROSTATE-CANCER-
dc.subject.keywordPlusDOWN-REGULATION-
dc.subject.keywordPlusGENES-
dc.subject.keywordPlusREIC/DKK-3-
dc.subject.keywordPlusMELANOMA-
dc.subject.keywordPlusSURVIVAL-
dc.subject.keywordPlusMUTATION-
dc.subject.keywordPlusBREAST-
dc.relation.journalResearchAreaOncology-
dc.relation.journalResearchAreaObstetrics & Gynecology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.relation.journalWebOfScienceCategoryObstetrics & Gynecology-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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