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Overview of major molecular alterations during progression from Barrett's esophagus to esophageal adenocarcinoma
Author(s) -
Kalatskaya Irina
Publication year - 2016
Publication title -
annals of the new york academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.712
H-Index - 248
eISSN - 1749-6632
pISSN - 0077-8923
DOI - 10.1111/nyas.13134
Subject(s) - esophagus , barrett's esophagus , cdh1 , dysplasia , cdkn2a , cancer , adenocarcinoma , biology , epithelium , pathology , cancer research , medicine , genetics , cadherin , cell
Esophageal adenocarcinoma (EAC) develops in the sequential transformation of normal epithelium into metaplastic epithelium, called Barrett's esophagus (BE), then to dysplasia, and finally cancer. BE is a common condition in which normal stratified squamous epithelium of the esophagus is replaced with an intestine‐like columnar epithelium, and it is the most prominent risk factor for EAC. This review aims to impartially systemize the knowledge from a large number of publications that describe the molecular and biochemical alterations occurring over this progression sequence. In order to provide an unbiased extraction of the knowledge from the literature, a text‐mining methodology was used to select genes that are involved in the BE progression, with the top candidate genes found to be TP53 , CDKN2A , CTNNB1 , CDH1 , GPX3 , and NOX5 . In addition, sample frequencies across analyzed patient cohorts at each stage of disease progression are summarized. All six genes are altered in the majority of EAC patients, and accumulation of alterations correlates well with the sequential progression of BE to cancer, indicating that the text‐mining method is a valid approach for gene prioritization. This review discusses how, besides being cancer drivers, these genes are functionally interconnected and might collectively be considered a central hub of BE progression.