| Literature DB >> 29055049 |
Zhaohui Xiong1,2, Shuang Ren1,2, Hao Chen2, Yao Liu1,2, Caizhi Huang2, Yawan Lyvia Zhang2, Joab Otieno Odera2, Tong Chen3, Ralf Kist4,5, Heiko Peters5, Katherine Garman6, Zheng Sun1, Xiaoxin Chen2,7.
Abstract
PAX9 is a transcription factor of the PAX family characterized by a DNA-binding paired domain. Previous studies have suggested a potential role of PAX9 in squamous cell differentiation and carcinogenesis of the oro-oesophageal epithelium. However, its functional roles in differentiation and carcinogenesis remain unclear. In this study, Pax9 deficiency in mouse oesophagus promoted cell proliferation, delayed cell differentiation, and altered the global gene expression profile. Ethanol exposure downregulated PAX9 expression in human oesophageal epithelial cells in vitro and mouse forestomach and tongue in vivo. We further showed that PAX9 was downregulated in human oro-oesophageal squamous cell carcinoma (OESCC), and its downregulation was associated with alcohol drinking and promoter hypermethylation. Moreover, ad libitum feeding with a liquid diet containing ethanol for 40 weeks or Pax9 deficiency promoted N-nitrosomethylbenzylamine-induced squamous cell carcinogenesis in mouse tongue, oesophagus, and forestomach. In conclusion, PAX9 regulates squamous cell differentiation in the oro-oesophageal epithelium. Alcohol drinking and promoter hypermethylation are associated with PAX9 silencing in human OESCC. PAX9 downregulation may contribute to alcohol-associated oro-oesophageal squamous cell carcinogenesis.Entities:
Keywords: PAX9; ethanol; oesophagus; promoter hypermethylation; squamous cell carcinoma
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Year: 2017 PMID: 29055049 PMCID: PMC5842438 DOI: 10.1002/path.4998
Source DB: PubMed Journal: J Pathol ISSN: 0022-3417 Impact factor: 7.996