Rustgi A K
Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
Gastroenterol Clin North Am. 1997 Sep;26(3):599-606. doi: 10.1016/s0889-8553(05)70316-2.
The biological mechanisms underlying the progression from normal esophageal squamous mucosa to Barrett's epithelium associated with dysplasia and finally to esophageal adenocarcinoma is becoming increasingly well understood. Histologic determination of Barrett's-associated dysplasia remains of paramount importance; however, genetic and biochemical biomarkers of Barrett's metaplasia and dysplasia will facilitate clinical diagnosis, endoscopic surveillance, and monitoring of new therapeutic interventions as they evolve. This article covers conventional and novel biomarkers in Barrett's esophagus.
从正常食管鳞状黏膜发展为伴有发育异常的巴雷特上皮并最终发展为食管腺癌的生物学机制正日益为人所理解。巴雷特相关发育异常的组织学判定仍然至关重要;然而,巴雷特化生和发育异常的遗传和生化生物标志物将有助于临床诊断、内镜监测以及随着新治疗干预措施的发展对其进行监测。本文涵盖了巴雷特食管中的传统和新型生物标志物。