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dc.contributor.authorGaykalova, Daria A.
dc.contributor.authorVatapalli, Rajita
dc.contributor.authorWei, Yingying
dc.contributor.authorTsai, Hua-Ling
dc.contributor.authorWang, Hao
dc.contributor.authorZhang, Chi
dc.contributor.authorHennessey, Patrick T.
dc.contributor.authorGuo, Theresa
dc.contributor.authorTan, Marietta
dc.contributor.authorLi, Ryan J.
dc.contributor.authorAhn, Julie
dc.contributor.authorKhan, Zubair
dc.contributor.authorWestra, William H.
dc.contributor.authorBishop, Justin A.
dc.contributor.authorZaboli, David
dc.contributor.authorKoch, Wayne M.
dc.contributor.authorKhan, Tanbir
dc.contributor.authorOchs, Michael F.
dc.contributor.authorCalifano, Joseph A.
dc.date.accessioned2018-04-21T15:59:03Z
dc.date.available2018-04-21T15:59:03Z
dc.date.issued2015
dc.identifier.citationGaykalova, D. A., Vatapalli, R., Wei, Y., Tsai, H., Wang, H., Zhang, C., & ... Califano, J. A. (2015). Outlier Analysis Defines Zinc Finger Gene Family DNA Methylation in Tumors and Saliva of Head and Neck Cancer Patients. Plos ONE, 10(10), 1-18.en_US
dc.identifier.urihttps://dx.doi.org/10.1371/journal.pone.0142148
dc.description.abstractHead and Neck Squamous Cell Carcinoma (HNSCC) is the fifth most common cancer, annually affecting over half a million people worldwide. Presently, there are no accepted biomarkers for clinical detection and surveillance of HNSCC. In this work, a comprehensive genome-wide analysis of epigenetic alterations in primary HNSCC tumors was employed in conjunction with cancer-specific outlier statistics to define novel biomarker genes which are differentially methylated in HNSCC. The 37 identified biomarker candidates were top-scoring outlier genes with prominent differential methylation in tumors, but with no signal in normal tissues. These putative candidates were validated in independent HNSCC cohorts from our institution and TCGA (The Cancer Genome Atlas). Using the top candidates, ZNF14, ZNF160, and ZNF420, an assay was developed for detection of HNSCC cancer in primary tissue and saliva samples with 100% specificity when compared to normal control samples. Given the high detection specificity, the analysis of ZNF DNA methylation in combination with other DNA methylation biomarkers may be useful in the clinical setting for HNSCC detection and surveillance, particularly in high-risk patients. Several additional candidates identified through this work can be further investigated toward future development of a multi-gene panel of biomarkers for the surveillance and detection of HNSCC.en_US
dc.language.isoen_USen_US
dc.publisherPublic Library of Scienceen_US
dc.titleOutlier Analysis Defines Zinc Finger Gene Family DNA Methylation in Tumors and Saliva of Head and Neck Cancer Patientsen_US
dc.typeArticleen_US
dc.typeTexten_US
prism.publicationNamePLOS ONE
prism.volume10
prism.issueIdentifier11
prism.publicationDate2015
dc.identifier.handlehttps://dr.tcnj.edu/handle/2900/2280


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