Outlier Analysis Defines Zinc Finger Gene Family DNA Methylation in Tumors and Saliva of Head and Neck Cancer Patients

被引:30
作者
Gaykalova, Daria A. [1 ]
Vatapalli, Rajita [1 ,2 ]
Wei, Yingying [3 ,4 ]
Tsai, Hua-Ling [3 ]
Wang, Hao [3 ]
Zhang, Chi [1 ,5 ]
Hennessey, Patrick T. [1 ]
Guo, Theresa [1 ]
Tan, Marietta [1 ]
Li, Ryan [1 ]
Ahn, Julie [1 ]
Khan, Zubair [1 ]
Westra, William H. [1 ,6 ]
Bishop, Justin A. [1 ,6 ]
Zaboli, David [1 ]
Koch, Wayne M. [1 ]
Khan, Tanbir [1 ]
Ochs, Michael F. [3 ,7 ]
Califano, Joseph A. [1 ,8 ,9 ]
机构
[1] Johns Hopkins Med Inst, Dept Otolaryngol Head & Neck Surg, Baltimore, MD 21205 USA
[2] Northwestern Univ, Dept Urol, Chicago, IL 60611 USA
[3] Johns Hopkins Med Inst, Dept Oncol, Div Oncol Biostat, Baltimore, MD 21205 USA
[4] Chinese Univ Hong Kong, Dept Stat, Shatin, Hong Kong, Peoples R China
[5] Univ Virginia, Dept Pathol, Charlottesville, VA 22903 USA
[6] Johns Hopkins Med Inst, Dept Pathol, Baltimore, MD 21205 USA
[7] Coll New Jersey, Dept Math & Stat, Ewing, NJ USA
[8] Greater Baltimore Med Ctr, Milton J Dance Head & Neck Ctr, Baltimore, MD USA
[9] Univ Calif San Diego, Dept Surg, Div Otolaryngol Head & Neck Surg, La Jolla, CA 92093 USA
来源
PLOS ONE | 2015年 / 10卷 / 11期
关键词
SQUAMOUS-CELL CARCINOMA; PROMOTER HYPERMETHYLATION; GLOBAL HYPOMETHYLATION; PROTEIN; ACTIVATION; EXPRESSION; BIOMARKER; BIOLOGY; RINSES; EDNRB;
D O I
10.1371/journal.pone.0142148
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Head 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.
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页数:18
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