Detailed Information

Cited 84 time in webofscience Cited 89 time in scopus
Metadata Downloads

Epithelial-mesenchymal transition in breast cancer correlates with high histological grade and triple-negative phenotype

Full metadata record
DC Field Value Language
dc.contributor.authorJeong, Hoiseon-
dc.contributor.authorRyu, Young-joon-
dc.contributor.authorAn, Jungsuk-
dc.contributor.authorLee, Youngseok-
dc.contributor.authorKim, Aeree-
dc.date.available2020-02-29T05:49:16Z-
dc.date.created2020-02-06-
dc.date.issued2012-05-
dc.identifier.issn0309-0167-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/16402-
dc.description.abstractAims: Epithelialmesenchymal transition (EMT) is characterized by a loss of epithelial nature and the acquisition of a mesenchymal form. The aim of this study was to assess the role of EMT in human mammary carcinogenesis, by performing immunohistochemical studies of EMT markers with tissue microarrays. Methods and results: A total of 492 cases were evaluated and classified as hormone receptor (HR)-positive type, HER2 type and triple-negative (TN) type by the use of immunohistochemistry and in-situ hybridization. We compared these groups in terms of epithelial and mesenchymal marker expression patterns. Of the 102 cases of TN-type breast cancer, 24.5% expressed vimentin, 13.7% expressed N-cadherin, and 9.8% expressed smooth muscle actin (SMA). Of the 221 cases of HR-type breast cancer, 4.1% expressed vimentin, 5.9% expressed N-cadherin, and 0.4% expressed SMA. Regarding epithelial markers, decreased expression was seen in 16.7% of cases for E-cadherin, in 45.1% for cytokeratin (CK)19 and in 60.8% for CK8 and CK18 (CAM5.2) in TN-type breast cancer cases. Decreased expression was seen in 11.8% of cases for E-cadherin, in 6.8% for CK19 and in 3.2% for CAM5.2 in HR-type cases. Conclusions: EMT features were particularly seen in TN-type breast cancer (P < 0.001). EMT was also significantly associated with high histological grade (P < 0.001).-
dc.language영어-
dc.language.isoen-
dc.publisherWILEY-BLACKWELL-
dc.relation.isPartOfHISTOPATHOLOGY-
dc.subjectBASAL-LIKE SUBTYPE-
dc.subjectSTEM-CELLS-
dc.subjectTGF-BETA-
dc.subjectTUMOR PROGRESSION-
dc.subjectUP-REGULATION-
dc.subjectCARCINOMA-
dc.subjectEMT-
dc.subjectMETASTASIS-
dc.subjectPATHWAYS-
dc.subjectSUPERIOR-
dc.titleEpithelial-mesenchymal transition in breast cancer correlates with high histological grade and triple-negative phenotype-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000303195600010-
dc.identifier.doi10.1111/j.1365-2559.2012.04195.x-
dc.identifier.bibliographicCitationHISTOPATHOLOGY, v.60, no.6B, pp.E87 - E95-
dc.identifier.scopusid2-s2.0-84862820130-
dc.citation.endPageE95-
dc.citation.startPageE87-
dc.citation.titleHISTOPATHOLOGY-
dc.citation.volume60-
dc.citation.number6B-
dc.contributor.affiliatedAuthorAn, Jungsuk-
dc.type.docTypeArticle-
dc.subject.keywordAuthorbreast-
dc.subject.keywordAuthorcarcinoma-
dc.subject.keywordAuthorepithelial-mesenchymal transition-
dc.subject.keywordAuthorimmunohistochemistry-
dc.subject.keywordAuthortissue array analysis-
dc.subject.keywordAuthortriple-negative-
dc.subject.keywordPlusBASAL-LIKE SUBTYPE-
dc.subject.keywordPlusSTEM-CELLS-
dc.subject.keywordPlusTGF-BETA-
dc.subject.keywordPlusTUMOR PROGRESSION-
dc.subject.keywordPlusUP-REGULATION-
dc.subject.keywordPlusCARCINOMA-
dc.subject.keywordPlusEMT-
dc.subject.keywordPlusMETASTASIS-
dc.subject.keywordPlusPATHWAYS-
dc.subject.keywordPlusSUPERIOR-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalResearchAreaPathology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.relation.journalWebOfScienceCategoryPathology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
Files in This Item
There are no files associated with this item.
Appears in
Collections
의과대학 > 의예과 > 1. Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Altmetrics

Total Views & Downloads

BROWSE