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Serum anti-GAPDH autoantibody levels reflect the severity of cervical lesions: A potential serum biomarker for cervical cancer screening

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dc.contributor.authorXu, Mei Ling-
dc.contributor.authorKim, Hyoung Jin-
dc.contributor.authorKim, Seung Cheol-
dc.contributor.authorJu, Woong-
dc.contributor.authorKim, Yun Hwan-
dc.contributor.authorChang, Kyu-Ho-
dc.contributor.authorKim, Hong-Jin-
dc.date.available2019-08-09T07:57:03Z-
dc.date.issued2019-07-
dc.identifier.issn1792-1074-
dc.identifier.issn1792-1082-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/32706-
dc.description.abstractRecent studies have indicated that a certain level of autoantibodies may be essential for maintaining good health as well as preventing cancer development, and that the levels of serum autoantibodies can decline during malignant progression. The aim of the present study was to identify such an autoantibody-based biomarker for screening cervical lesions. An autoantigen reactive with healthy female sera was detected in the cytosolic fraction of HeLa cells, a cervical cancer cell line, and identified. Serum immunoglobulin (Ig)-G and IgM levels against the purified autoantigen in normal, cervical intraepithelial neoplasias (CINs) I, II and III, and cervical cancer were compared using ELISAs. The autoantigen in HeLa cells was identified to be GAPDH. The serum levels of anti-HeLa-GAPDH IgG decreased with increasing severity of cervical lesions, and similar decreases in IgM levels were revealed. Notably, the anti-HeLa-GAPDH IgG level was discovered to discriminate cervical cancer from normal samples with 80.0% sensitivity and 96.6% specificity. The serum anti-HeLa-GAPDH autoantibody level, as a single parameter, is a promising serum biomarker for screening cervical lesions.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherSPANDIDOS PUBL LTD-
dc.titleSerum anti-GAPDH autoantibody levels reflect the severity of cervical lesions: A potential serum biomarker for cervical cancer screening-
dc.typeArticle-
dc.identifier.doi10.3892/ol.2019.10326-
dc.identifier.bibliographicCitationONCOLOGY LETTERS, v.18, no.1, pp 255 - 264-
dc.description.isOpenAccessN-
dc.identifier.wosid000474896900031-
dc.identifier.scopusid2-s2.0-85068888685-
dc.citation.endPage264-
dc.citation.number1-
dc.citation.startPage255-
dc.citation.titleONCOLOGY LETTERS-
dc.citation.volume18-
dc.type.docTypeArticle-
dc.publisher.location그리이스-
dc.subject.keywordAuthorautoantibody-
dc.subject.keywordAuthorglyceraldehyde 3-phosphate dehydrogenase-
dc.subject.keywordAuthorcervical cancer-
dc.subject.keywordAuthorcervical intraepithelial neoplasia-
dc.subject.keywordAuthorserum biomarker-
dc.subject.keywordPlusGLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE GENE-
dc.subject.keywordPlusTUMOR-ASSOCIATED ANTIGENS-
dc.subject.keywordPlusHUMAN-PAPILLOMAVIRUS-
dc.subject.keywordPlusNATURAL-HISTORY-
dc.subject.keywordPlusRADICAL HYSTERECTOMY-
dc.subject.keywordPlusIGM ANTIBODIES-
dc.subject.keywordPlusSURVIVAL RATE-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusRISK-
dc.subject.keywordPlusPROLIFERATION-
dc.relation.journalResearchAreaOncology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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