Signaling Pathways in the Pathogenesis of Barrett’s Esophagus and Esophageal Adenocarcinoma

Barrett’s esophagus (BE) is a premalignant lesion that can develop into esophageal adenocarcinoma (EAC). The development of Barrett’s esophagus is caused by biliary reflux, which causes extensive mutagenesis in the stem cells of the epithelium in the distal esophagus and gastro-esophageal junction. Other possible cellular origins of BE include the stem cells of the mucosal esophageal glands and their ducts, the stem cells of the stomach, residual embryonic cells and circulating bone marrow stem cells. The classical concept of healing a caustic lesion has been replaced by the concept of a cytokine storm, which forms an inflammatory microenvironment eliciting a phenotypic shift toward intestinal metaplasia of the distal esophagus. This review describes the roles of the NOTCH, hedgehog, NF-κB and IL6/STAT3 molecular pathways in the pathogenesis of BE and EAC. © 2023 by the authors.

Авторы
Maslenkina K. , Mikhaleva L. , Naumenko M. , Vandysheva R. , Gushchin M. , Atiakshin D. , Buchwalow I. , Tiemann M.
Издательство
MDPI AG
Номер выпуска
11
Язык
Английский
Статус
Опубликовано
Номер
9304
Том
24
Год
2023
Организации
  • 1 A.P. Avtsyn Research Institute of Human Morphology, Petrovsky National Research Center of Surgery, Moscow, 119991, Russian Federation
  • 2 Research and Educational Resource Centre for Immunophenotyping, Digital Spatial Profiling and Ultrastructural Analysis Innovative Technologies, Peoples’ Friendship University of Russia Named after Patrice Lumumba, Moscow, 117198, Russian Federation
  • 3 Institute for Hematopathology, Fangdieckstr. 75a, Hamburg, 22547, Germany
Ключевые слова
Barrett’s esophagus; carcinogenesis; dysplasia; esophageal adenocarcinoma; inflammatory signaling pathways; intestinal metaplasia; mutational load; p53
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