Publication:
Evaluation of NID2 promoter methylation for screening of Oral squamous cell carcinoma

dc.contributor.authorRatakorn Srisutteeen_US
dc.contributor.authorAreeya Arayataweegoolen_US
dc.contributor.authorPatnarin Mahattanasakulen_US
dc.contributor.authorNapadon Tangjaturonrasmeen_US
dc.contributor.authorVirachai Kerekhanjanarongen_US
dc.contributor.authorSomboon Keelawaten_US
dc.contributor.authorApiwat Mutiranguraen_US
dc.contributor.authorNakarin Kitkumthornen_US
dc.contributor.otherChulalongkorn Universityen_US
dc.contributor.otherKing Chulalongkorn Memorial Hospital, Faculty of Medicine Chulalongkorn Universityen_US
dc.contributor.otherKing Mongkut's Institute of Technology Ladkrabangen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2020-03-26T04:29:56Z
dc.date.available2020-03-26T04:29:56Z
dc.date.issued2020-03-14en_US
dc.description.abstract© 2020 The Author(s). Background: Oral squamous cell carcinoma (OSCC) is an aggressive human malignancy. Because of late diagnosis and recurrence of OSCC, the treatment of patients with OSCC is often ineffective. Thus, finding novel biomarkers of OSCC are essential. Here we derived a methylation marker by utilizing methylation microarray data and testing its capacity in cross-sectional study designed for OSCC detection and screening. Methods: According to bioinformatics analysis of total of 27,578 cg sites, cg22881914 of Nidogen 2 (NID2) methylation was selected for evaluation. Next, we confirmed the methylation status by bisulfite sequencing from the microdissected OSCC cells in comparison with the microdissected oral epithelia. Subsequently, we developed a simple technique using real-time PCR with the specific probe to examine the ability for the detection of OSCC in the oral epithelial samples, which included 103 oral rinse and 82 oral swab samples. Results: Based on the comparison of microdissected tissue, cg22881914 of NID2 was proved to be methylated in most OSCC cells but unmethylated in the normal oral epithelia. Furthermore, the methylated NID2-relied quantitative PCR approach has demonstrated that this marker assists in distinguishing among patients with OSCC from normal oral epithelia, smokers, and patients with oral lichen planus using the non-invasive oral rinse and swab samples. Conclusions: Specific methylation at cg22881914 of NID2 of OSCC could be used as an important potential marker for detecting OSCC. Thus, to certify the utility of this marker, further studies with a larger sample size are needed.en_US
dc.identifier.citationBMC Cancer. Vol.20, No.1 (2020)en_US
dc.identifier.doi10.1186/s12885-020-6692-zen_US
dc.identifier.issn14712407en_US
dc.identifier.other2-s2.0-85081743934en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/53566
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85081743934&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleEvaluation of NID2 promoter methylation for screening of Oral squamous cell carcinomaen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85081743934&origin=inwarden_US

Files

Collections