DNA methylation regulates TMEM16A/ANO1 expression through multiple CpG islands in head and neck squamous cell carcinoma

DNA甲基化 CpG站点 头颈部鳞状细胞癌 甲基化 表观遗传学 癌症研究 生物 转染 基因表达调控 表观遗传学 基因表达 分子生物学 癌症 基因 头颈部癌 遗传学
作者
Andrey Finegersh,Scott Kulich,Theresa Guo,Alexander V. Favorov,Elana J. Fertig,Ludmila Danilova,Daria A. Gaykalova,Joseph A. Califano,Umamaheswar Duvvuri
出处
期刊:Scientific Reports [Springer Nature]
卷期号:7 (1) 被引量:24
标识
DOI:10.1038/s41598-017-15634-9
摘要

ANO1 is a calcium-activated chloride channel that is frequently overexpressed in head and neck squamous cell carcinoma (HNSCC) and other cancers. While ANO1 expression negatively correlates with survival in several cancers, its epigenetic regulation is poorly understood. We analyzed HNSCC samples from TCGA and a separate dataset of HPV+ oropharyngeal squamous cell carcinoma (OPSCC) samples to identify differentially methylated regions. E6 and E7 transfected normal oral keratinocytes (NOK) were used to induce hypermethylation of the ANO1 promoter. We found three CpG islands that correlated with ANO1 expression, including two positively correlated with expression. Using two HNSCC datasets with differential expression of ANO1, we showed hypermethylation of positively correlated CpG islands potentiates ANO1 expression. E7 but not E6 transfection of NOK cells led to hypermethylation of a positively correlated CpG island without a change in ANO1 expression. ANO1 promoter methylation was also correlated with patient survival. Our results are the first to show the contribution of positively correlated CpG's for regulating gene expression in HNSCC. Hypermethylation of the ANO1 promoter was strongly correlated with but not sufficient to increase ANO1 expression, suggesting methylation of positively correlated CpG's likely serves as an adjunct to other mechanisms of ANO1 activation.
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