234 481

Cited 44 times in

Expression of Lipid Metabolism-Related Proteins in Metastatic Breast Cancer

DC Field Value Language
dc.contributor.author구자승-
dc.contributor.author정윤양-
dc.contributor.author김혜민-
dc.date.accessioned2016-02-04T11:43:06Z-
dc.date.available2016-02-04T11:43:06Z-
dc.date.issued2015-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/141044-
dc.description.abstractPURPOSE: The tumor biology of metastatic breast cancers differ according to the metastatic sites, and the features of cancer metabolism may also be different. The aim of this study is to investigate the expression of lipid metabolism-related proteins in metastatic breast cancer according to metastatic site and discuss the clinical significance thereof. METHODS: Immunohistochemical staining for lipid metabolism-related proteins [fatty acid synthase (FASN), hormone-sensitive lipase (HSL), carnitine palmitoyltransferase IA (CPT-1A), acyl-CoA oxidase 1 (ACOX1), fatty acid binding protein 4 (FABP4,) and perilipin 1 (PLIN1)] was performed using a tissue microarray of 149 cases of metastatic breast cancer (bone metastasis = 39, brain metastasis = 37, liver metastasis = 21, and lung metastasis = 52). RESULTS: The expression levels of ACOX1 (p = 0.009) and FASN (p = 0.007) varied significantly according to metastatic site, with the highest expression in brain metastasis and the lowest expression in liver metastasis. ACOX1 positivity (p = 0.005) and FASN positivity (p = 0.003) correlated with HER-2 positivity. The expression of FASN was significantly higher in HER-2 type breast cancer, and lower in luminal A and TNBC type breast cancer (p<0.001). Among lipid metabolism-related proteins, PLIN1 positivity was found to be an independent poor prognostic factor on multivariate analysis (Hazard ratio: 4.979, 95% CI: 1.054-22.59, p = 0.043). CONCLUSION: Different expression levels of lipid metabolism-related proteins were observed according to metastatic site. The expression of ACOX1 and FASN was highest in brain metastasis. These results suggest that the metastatic site should be considered when using lipid metabolism inhibitors for targeted therapy.-
dc.description.statementOfResponsibilityopen-
dc.formatapplication/pdf-
dc.relation.isPartOfPLOS ONE-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAcyl-CoA Oxidase/biosynthesis-
dc.subject.MESHAcyl-CoA Oxidase/genetics-
dc.subject.MESHAdult-
dc.subject.MESHBone Neoplasms/metabolism-
dc.subject.MESHBone Neoplasms/secondary-
dc.subject.MESHBrain Neoplasms/metabolism-
dc.subject.MESHBrain Neoplasms/secondary-
dc.subject.MESHBreast Neoplasms/genetics-
dc.subject.MESHBreast Neoplasms/metabolism*-
dc.subject.MESHBreast Neoplasms/pathology-
dc.subject.MESHCarcinoma/genetics-
dc.subject.MESHCarcinoma/metabolism-
dc.subject.MESHCarcinoma/secondary*-
dc.subject.MESHCarnitine O-Palmitoyltransferase/biosynthesis-
dc.subject.MESHCarnitine O-Palmitoyltransferase/genetics-
dc.subject.MESHCarrier Proteins/biosynthesis-
dc.subject.MESHCarrier Proteins/genetics-
dc.subject.MESHEstrogens-
dc.subject.MESHFatty Acid Synthase, Type I/biosynthesis-
dc.subject.MESHFatty Acid Synthase, Type I/genetics-
dc.subject.MESHFatty Acid-Binding Proteins/biosynthesis-
dc.subject.MESHFatty Acid-Binding Proteins/genetics-
dc.subject.MESHFemale-
dc.subject.MESHGene Expression Regulation, Neoplastic*-
dc.subject.MESHGenes, erbB-2-
dc.subject.MESHHumans-
dc.subject.MESHKaplan-Meier Estimate-
dc.subject.MESHLipid Metabolism/genetics*-
dc.subject.MESHLiver Neoplasms/metabolism-
dc.subject.MESHLiver Neoplasms/secondary-
dc.subject.MESHLung Neoplasms/metabolism-
dc.subject.MESHLung Neoplasms/secondary-
dc.subject.MESHMiddle Aged-
dc.subject.MESHNeoplasm Proteins/biosynthesis-
dc.subject.MESHNeoplasm Proteins/genetics-
dc.subject.MESHNeoplasms, Hormone-Dependent/genetics-
dc.subject.MESHNeoplasms, Hormone-Dependent/metabolism-
dc.subject.MESHOrgan Specificity-
dc.subject.MESHPerilipin-1-
dc.subject.MESHPhosphoproteins/biosynthesis-
dc.subject.MESHPhosphoproteins/genetics-
dc.subject.MESHProgesterone-
dc.subject.MESHProportional Hazards Models-
dc.subject.MESHReceptor, ErbB-2/analysis-
dc.subject.MESHTriple Negative Breast Neoplasms/genetics-
dc.subject.MESHTriple Negative Breast Neoplasms/metabolism-
dc.titleExpression of Lipid Metabolism-Related Proteins in Metastatic Breast Cancer-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Pathology (병리학)-
dc.contributor.googleauthorYoon Yang Jung-
dc.contributor.googleauthorHye Min Kim-
dc.contributor.googleauthorJa Seung Koo-
dc.identifier.doi10.1371/journal.pone.0137204-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00198-
dc.contributor.localIdA03681-
dc.relation.journalcodeJ02540-
dc.identifier.eissn1932-6203-
dc.identifier.pmid26334757-
dc.contributor.alternativeNameKoo, Ja Seung-
dc.contributor.alternativeNameJung, Yoon Yang-
dc.contributor.affiliatedAuthorKoo, Ja Seung-
dc.contributor.affiliatedAuthorJung, Yoon Yang-
dc.contributor.affiliatedAuthor구자승-
dc.rights.accessRightsfree-
dc.citation.volume10-
dc.citation.number9-
dc.citation.startPagee0137204-
dc.identifier.bibliographicCitationPLOS ONE, Vol.10(9) : e0137204, 2015-
dc.identifier.rimsid30478-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers

qrcode

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