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Fibronectin on circulating extracellular vesicles as a liquid biopsy to detect breast cancer

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dc.contributor.authorMoon, Pyong-Gon-
dc.contributor.authorLee, Jeong-Eun-
dc.contributor.authorCho, Young-Eun-
dc.contributor.authorLee, Soo Jung-
dc.contributor.authorChae, Yee Soo-
dc.contributor.authorJung, Jin Hyang-
dc.contributor.authorKim, In-San-
dc.contributor.authorPark, Ho Yong-
dc.contributor.authorBaek, Moon-Chang-
dc.date.accessioned2021-09-03T22:39:04Z-
dc.date.available2021-09-03T22:39:04Z-
dc.date.created2021-06-18-
dc.date.issued2016-06-28-
dc.identifier.issn1949-2553-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/88297-
dc.description.abstractExtracellular vesicles (EVs) secreted from cancer cells have potential for generating cancer biomarker signatures. Fibronectin (FN) was selected as a biomarker candidate, due to the presence in surface on EVs secreted from human breast cancer cell lines. A subsequent study used two types of enzyme-linked immunosorbent assays (ELISA) to determine the presence of these proteins in plasma samples from disease-free individuals (n=70), patients with BC (n=240), BC patients after surgical resection (n=40), patients with benign breast tumor (n=55), and patients with non-cancerous diseases (thyroiditis, gastritis, hepatitis B, and rheumatoid arthritis; n=80). FN levels were significantly elevated (p<.0001) at all stages of BC, and returned to normal after tumor removal. The diagnostic accuracy for FN detection in extracellular vesicles (ELISA method 1) (area under the curve, 0.81; 95% CI, 0.76 to 0.86; sensitivity of 65.1% and specificity of 83.2%) were also better than those for FN detection in the plasma (ELISA method 2) (area under the curve, 0.77; 95% CI, 0.72 to 0.83; sensitivity of 69.2% and specificity of 73.3%) in BC. The diagnostic accuracy of plasma FN was similar in both the early-stage BC and all BC patients, as well as in the two sets. This liquid biopsy to detect FN on circulating EVs could be a promising method to detect early breast cancer.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherIMPACT JOURNALS LLC-
dc.subjectCELL-MIGRATION-
dc.subjectINTEGRIN REGULATION-
dc.subjectURINARY EXOSOMES-
dc.subjectOVARIAN-CANCER-
dc.subjectMICROVESICLES-
dc.subjectINVASION-
dc.subjectMETASTASIS-
dc.subjectBIOMARKERS-
dc.subjectPROTEOMICS-
dc.subjectPATHWAYS-
dc.titleFibronectin on circulating extracellular vesicles as a liquid biopsy to detect breast cancer-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, In-San-
dc.identifier.doi10.18632/oncotarget.9561-
dc.identifier.scopusid2-s2.0-84982995063-
dc.identifier.wosid000378614700096-
dc.identifier.bibliographicCitationONCOTARGET, v.7, no.26, pp.40189 - 40199-
dc.relation.isPartOfONCOTARGET-
dc.citation.titleONCOTARGET-
dc.citation.volume7-
dc.citation.number26-
dc.citation.startPage40189-
dc.citation.endPage40199-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.subject.keywordPlusCELL-MIGRATION-
dc.subject.keywordPlusINTEGRIN REGULATION-
dc.subject.keywordPlusURINARY EXOSOMES-
dc.subject.keywordPlusOVARIAN-CANCER-
dc.subject.keywordPlusMICROVESICLES-
dc.subject.keywordPlusINVASION-
dc.subject.keywordPlusMETASTASIS-
dc.subject.keywordPlusBIOMARKERS-
dc.subject.keywordPlusPROTEOMICS-
dc.subject.keywordPlusPATHWAYS-
dc.subject.keywordAuthorbreast cancer-
dc.subject.keywordAuthordiagnosis-
dc.subject.keywordAuthorextracellular vesicle-
dc.subject.keywordAuthorELISA-
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