Cancer Risk in Barrett's Esophagus: A Clinical Review

被引:10
|
作者
Beydoun, Ahmed Sam [1 ]
Stabenau, Kaleigh A. [1 ]
Altman, Kenneth W. [2 ]
Johnston, Nikki [1 ]
机构
[1] Med Coll Wisconsin, Dept Otolaryngol & Commun Sci, Milwaukee, WI 53226 USA
[2] Geisinger Med Ctr, Dept Otolaryngol Head & Neck Surg, Danville, PA 17822 USA
关键词
Barrett's esophagus; esophageal adenocarcinoma; gastroesophageal reflux disease; cancer; RNA sequencing; molecular pathways; LOW-GRADE DYSPLASIA; HELICOBACTER-PYLORI INFECTION; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; GASTROESOPHAGEAL REFLUX DISEASE; BODY-MASS INDEX; INTESTINAL METAPLASIA; ESOPHAGOGASTRIC JUNCTION; GOBLET CELLS; ENDOSCOPIC SURVEILLANCE; RADIOFREQUENCY ABLATION;
D O I
10.3390/ijms24076018
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Esophageal adenocarcinoma (EAC) is rapidly increasing in incidence and is associated with a poor prognosis. Barrett's esophagus (BE) is a known precursor of esophageal adenocarcinoma. This review aims to explore Barrett's esophagus, esophageal adenocarcinoma, and the progression from the former to the latter. An overview of the definition, diagnosis, epidemiology, and risk factors for both entities are presented, with special attention being given to the areas of debate in the literature. The progression from Barrett's esophagus to esophageal adenocarcinoma is reviewed and the relevant molecular pathways are discussed. The definition of Barrett's esophagus remains debated and without international consensus. This, alongside other factors, has made establishing the true prevalence of Barrett's esophagus challenging. The degree of dysplasia can be a histological challenge, but is necessary to guide clinical management. The progression of BE to EAC is likely driven by inflammatory pathways, pepsin exposure, upregulation of growth factor pathways, and mitochondrial changes. Surveillance is maintained through serial endoscopic evaluation, with shorter intervals recommended for high-risk features.
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页数:17
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