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The role of hLHX6-HMR as a methylation biomarker for early diagnosis of cervical cancer

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dc.contributor.authorJung, Samil-
dc.contributor.authorJeong, Dongjun-
dc.contributor.authorKim, Jinsun-
dc.contributor.authorYi, Lisha-
dc.contributor.authorKoo, Keunhoe-
dc.contributor.authorLee, Jaehyouk-
dc.contributor.authorLee, Soon-Duck-
dc.contributor.authorPark, Jin-Wha-
dc.contributor.authorChang, Boogi-
dc.contributor.authorKim, Chang-Hwan-
dc.contributor.authorKim, Chang-Jin-
dc.contributor.authorLee, Myeong-Sok-
dc.date.available2021-02-22T13:47:50Z-
dc.date.issued2010-06-
dc.identifier.issn1021-335X-
dc.identifier.issn1791-2431-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/13199-
dc.description.abstractThe homo sapiens LIM homeobox domain LHX6 gene, hLHX6, is a putative transcription regulator with homeodomain. Multiple cytosine guanine dinucleotides (CpG island) are found in the genomic sequences between exon 4a and exon 5 of the gene encoding hLHX6s (alternative short isoform of hLHX6 gene). This specific CpG island, hLHX6-HMR, is found frequently hypermethylated in 7 cervical cancer cell lines as shown in MSP, BSP, and COBRA assays. Methylation densities were also investigated with human tissue 'samples with a distinctive degree of malignant transformation. Our data showed that the hLHX6-HMR was rarely or partly methylated in the normal and CIN I cells, respectively. In contrast, it was frequently hypermethylated in CIN II, CIN III, and invasive carcinoma cells. In summary, this methylation study led to two conclusions. First, hLHX6-HMR hypermethylation is exclusively associated with cervical carcinogenesis. Second, the epigenetic change in hLHX6-HMR seems to start at CIN I, relatively early stage of cervical cancer development. Therefore, hLHX6-HMR can be used as an effective and sensitive methylation biomarker for early diagnosis of cervical cancer.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherSPANDIDOS PUBL LTD-
dc.titleThe role of hLHX6-HMR as a methylation biomarker for early diagnosis of cervical cancer-
dc.typeArticle-
dc.publisher.location그리이스-
dc.identifier.doi10.3892/or_00000811-
dc.identifier.scopusid2-s2.0-77951729708-
dc.identifier.wosid000277526800025-
dc.identifier.bibliographicCitationONCOLOGY REPORTS, v.23, no.6, pp 1675 - 1682-
dc.citation.titleONCOLOGY REPORTS-
dc.citation.volume23-
dc.citation.number6-
dc.citation.startPage1675-
dc.citation.endPage1682-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.subject.keywordPlusHUMAN-PAPILLOMAVIRUS-
dc.subject.keywordPlusDNA-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusNEOPLASIA-
dc.subject.keywordAuthorepigenetics-
dc.subject.keywordAuthormcthylation biomarker-
dc.subject.keywordAuthorcervical cancer-
dc.subject.keywordAuthorhLHX6-HMR-
dc.identifier.urlhttps://www.spandidos-publications.com/or/23/6/1675-
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