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J Pathol ; 253(4): 384-395, 2021 04.
Article in English | MEDLINE | ID: mdl-33314197

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. © 2020 The Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.


Subject(s)
Alcohol Drinking/adverse effects , Esophageal Squamous Cell Carcinoma/pathology , PAX9 Transcription Factor/drug effects , Receptors, Notch/drug effects , Squamous Cell Carcinoma of Head and Neck/pathology , Animals , Epithelial Cells/drug effects , Epithelial Cells/metabolism , Esophageal Squamous Cell Carcinoma/metabolism , Ethanol/toxicity , Humans , Mice , PAX9 Transcription Factor/metabolism , Receptors, Notch/metabolism , Signal Transduction/drug effects , Squamous Cell Carcinoma of Head and Neck/metabolism
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