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Yes-associated protein (YAP) is differentially expressed in tumor and stroma according to the molecular subtype of breast cancer.

DC Field Value Language
dc.contributor.author구자승-
dc.contributor.author김상겸-
dc.contributor.author정우희-
dc.date.accessioned2015-01-06T16:59:39Z-
dc.date.available2015-01-06T16:59:39Z-
dc.date.issued2014-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/99167-
dc.description.abstractIn this study, we aimed to clarify the expression profiles of Yes-associated protein (YAP) and phosphorylated YAP (pYAP) protein and to verify the clinical implication of the expression of YAP protein in human breast cancer. We selected 678 cases of formalin-fixed paraffin-embedded (FFPE) breast cancer tissue to construct tissue microarray (TMA) blocks. We performed immunohistochemical staining of estrogen receptor (ER), progesterone receptor (PR), human epidermal growth receptor-2 (HER-2) and Ki-67 and fluorescent in situ hybridization (FISH) assay for HER-2 on the TMA sections and divided breast cancers into molecular subtypes: luminal A, luminal B, HER-2, triple negative breast cancer (TNBC). Then, we examined YAP and pYAP expression status using immunohistochemical analysis according to the molecular subtypes of breast cancer. We found that HER-2 type breast cancer demonstrated elevated expression level in tumoral cytoplasmic YAP (P = 0.011) and pYAP (P = 0.049). Expressions of stromal YAP (P = 0.002) and pYAP (P < 0.001) were higher in luminal B and HER-2 type breast cancer but lower in TNBC. In univariate analysis, nuclear YAP expression of tumor cells was associated with shorter overall survival (OS) (P = 0.024). Cytoplasmic YAP expression of HER-2 type breast cancer cells negatively affected disease-free survival (DFS) (P = 0.034). In conclusion, we concluded that there was a significant difference in YAP and pYAP expression status according to molecular subtypes and tumoral and cellular components of breast cancers. Finally, we found that nuclear and cytoplasmic YAP expression could be a prognostic marker for breast cancer patients.-
dc.description.statementOfResponsibilityopen-
dc.format.extent3224~3234-
dc.relation.isPartOfINTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdaptor Proteins, Signal Transducing/analysis-
dc.subject.MESHAdaptor Proteins, Signal Transducing/biosynthesis*-
dc.subject.MESHBiomarkers, Tumor/analysis-
dc.subject.MESHBreast Neoplasms/metabolism-
dc.subject.MESHBreast Neoplasms/mortality-
dc.subject.MESHBreast Neoplasms/pathology*-
dc.subject.MESHDisease-Free Survival-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHImmunohistochemistry-
dc.subject.MESHIn Situ Hybridization, Fluorescence-
dc.subject.MESHKaplan-Meier Estimate-
dc.subject.MESHKi-67 Antigen/biosynthesis-
dc.subject.MESHPhenotype-
dc.subject.MESHPhosphoproteins/analysis-
dc.subject.MESHPhosphoproteins/biosynthesis*-
dc.subject.MESHPhosphorylation-
dc.subject.MESHProportional Hazards Models-
dc.subject.MESHReceptor, ErbB-2/biosynthesis-
dc.subject.MESHReceptors, Estrogen/biosynthesis-
dc.subject.MESHReceptors, Progesterone/biosynthesis-
dc.subject.MESHTissue Array Analysis-
dc.subject.MESHTumor Microenvironment*-
dc.titleYes-associated protein (YAP) is differentially expressed in tumor and stroma according to the molecular subtype of breast cancer.-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Pathology (병리학)-
dc.contributor.googleauthorSang Kyum Kim-
dc.contributor.googleauthorWoo Hee Jung-
dc.contributor.googleauthorJa Seung Koo-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00198-
dc.contributor.localIdA00520-
dc.contributor.localIdA03671-
dc.relation.journalcodeJ01096-
dc.identifier.eissn1936-2625-
dc.identifier.pmid25031743-
dc.subject.keywordBreast cancer-
dc.subject.keywordYAP-
dc.subject.keywordmolecular subtype-
dc.contributor.alternativeNameKoo, Ja Seung-
dc.contributor.alternativeNameKim, Sang Kyum-
dc.contributor.alternativeNameJung, Woo Hee-
dc.contributor.affiliatedAuthorKoo, Ja Seung-
dc.contributor.affiliatedAuthorKim, Sang Kyum-
dc.contributor.affiliatedAuthorJung, Woo Hee-
dc.contributor.affiliatedAuthor구자승-
dc.citation.volume7-
dc.citation.number6-
dc.citation.startPage3224-
dc.citation.endPage3234-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY, Vol.7(6) : 3224-3234, 2014-
dc.identifier.rimsid51191-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers

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