Detailed Information

Cited 0 time in webofscience Cited 0 time in scopus
Metadata Downloads

CYR61 confers chemoresistance by upregulating survivin expression in triple-negative breast cancer

Full metadata record
DC Field Value Language
dc.contributor.authorKim, Hyungjoo-
dc.contributor.authorSon, Seogho-
dc.contributor.authorKo, Yunhyo-
dc.contributor.authorLim, Hogeun-
dc.contributor.authorLee, Joohyung-
dc.contributor.authorLee, Kyung-Min-
dc.contributor.authorShin, Incheol-
dc.date.accessioned2024-11-28T16:31:22Z-
dc.date.available2024-11-28T16:31:22Z-
dc.date.issued2024-07-
dc.identifier.issn0143-3334-
dc.identifier.issn1460-2180-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/197680-
dc.description.abstractCysteine-rich angiogenic inducer 61 (CYR61) is a protein from the CCN family of matricellular proteins that play diverse regulatory roles in the extracellular matrix. CYR61 is involved in cell adhesion, migration, proliferation, differentiation, apoptosis, and senescence. Here, we show that CYR61 induces chemoresistance in triple-negative breast cancer (TNBC). We observed that CYR61 is overexpressed in TNBC patients, and CYR61 expression correlates negatively with the survival of patients who receive chemotherapy. CYR61 knockdown reduced cell migration, sphere formation and the cancer stem cell (CSC) population and increased the chemosensitivity ofTNBC cells. Mechanistically, CYR61 activated Wnt/β-catenin signaling and increased survivin expression, which are associated with chemoresistance, the epithelial–mesenchymal transition, and CSC-like phenotypes. Altogether, our study demonstrates a novel function of CYR61 in chemotherapy resistance in breast cancer.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherOxford University Press-
dc.titleCYR61 confers chemoresistance by upregulating survivin expression in triple-negative breast cancer-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1093/carcin/bgae013-
dc.identifier.scopusid2-s2.0-85198285486-
dc.identifier.wosid001187095900001-
dc.identifier.bibliographicCitationCarcinogenesis, v.45, no.7, pp 510 - 519-
dc.citation.titleCarcinogenesis-
dc.citation.volume45-
dc.citation.number7-
dc.citation.startPage510-
dc.citation.endPage519-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.subject.keywordPlusDRUG-RESISTANCE-
dc.subject.keywordPlusCELL-SURVIVAL-
dc.subject.keywordPlusSTEM-CELLS-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordPlusMETASTASIS-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusTRANSITION-
dc.subject.keywordPlusPATHWAY-
dc.subject.keywordPlusGENES-
dc.identifier.urlhttps://academic.oup.com/carcin/article/45/7/510/7623282?login=true-
Files in This Item
Go to Link
Appears in
Collections
서울 자연과학대학 > 서울 생명과학과 > 1. Journal Articles

qrcode

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

Related Researcher

Researcher Shin, In cheol photo

Shin, In cheol
COLLEGE OF NATURAL SCIENCES (DEPARTMENT OF LIFE SCIENCE)
Read more

Altmetrics

Total Views & Downloads

BROWSE