| Literature DB >> 33314197 |
Menghan Shi1,2, Shuang Ren1,2, Hao Chen2, Jing Li2,3, Caizhi Huang2, Yahui Li2, Yuning Han3, Yong Li4, Zheng Sun1, Xiaoxin Chen2,5, Zhaohui Xiong2.
Abstract
Alcohol drinking has been established as a major risk factor for esophageal diseases. Our previous study showed that ethanol exposure inhibited PAX9 expression in human esophageal squamous epithelial cells in vitro and in vivo. In this study, we aimed to investigate the molecular pathways through which alcohol drinking suppresses PAX9 in esophageal squamous epithelial cells. We first demonstrated the inhibition of NOTCH by ethanol exposure in vitro. NOTCH regulated PAX9 expression in KYSE510 and KYSE410 cells in vitro and in vivo. RBPJ and NOTCH intracellular domain (NIC) D1 ChIP-PCR confirmed Pax9 as a direct downstream target of NOTCH signaling in mouse esophagus. NOTCH inhibition by alcohol drinking was further validated in mouse esophagus and human tissue samples. In conclusion, ethanol exposure inhibited NOTCH signaling and thus suppressed PAX9 expression in esophageal squamous epithelial cells in vitro and in vivo. Our data support a novel mechanism of alcohol-induced esophageal injury through the inhibition of NOTCH-PAX9 signaling.Entities:
Keywords: NICD1; NOTCH; PAX9; RBPJ; esophageal squamous cell carcinoma; esophagus; ethanol
Year: 2021 PMID: 33314197 PMCID: PMC7987830 DOI: 10.1002/path.5602
Source DB: PubMed Journal: J Pathol ISSN: 0022-3417 Impact factor: 7.996