Garman Katherine S
Department of Medicine Division of Gastroenterology, Duke University Medical Center, Durham, North Carolina.
Cell Mol Gastroenterol Hepatol. 2017 Mar 6;4(1):153-156. doi: 10.1016/j.jcmgh.2017.01.016. eCollection 2017 Jul.
The origin of the progenitor cell for Barrett's esophagus remains a major unsolved mystery. Understanding the source of this progenitor may improve strategies to prevent the development of esophageal adenocarcinoma. Esophageal submucosal glands (ESMGs) and ducts may serve as a potential source of progenitor cells that respond to esophageal injury. Through the use of human histologic and molecular analysis, ESMGs and ducts have been described in physical continuity with areas of columnar esophagus, and shared mutations have been described between ESMG ducts and Barrett's esophagus. Acinar ductal metaplasia, associated with carcinogenesis in other organs, occurs within ESMGs with human esophageal injury and esophageal adenocarcinoma. By using atypical animal models, a squamous epithelial defect well above the gastroesophageal junction healed to columnar epithelium and continuity of ESMG ducts was noted in the new epithelium. Increased proliferation in ESMGs and ducts in response to injury also has been noted in human beings and animals.
巴雷特食管祖细胞的起源仍是一个主要的未解之谜。了解这种祖细胞的来源可能会改进预防食管腺癌发生的策略。食管黏膜下腺(ESMGs)和导管可能是对食管损伤作出反应的祖细胞的潜在来源。通过人类组织学和分子分析,已发现ESMGs和导管与柱状食管区域存在物理连续性,并且在ESMG导管和巴雷特食管之间发现了共同的突变。在人类食管损伤和食管腺癌的ESMGs中会出现与其他器官致癌作用相关的腺泡导管化生。通过使用非典型动物模型,在高于胃食管交界处的鳞状上皮缺损处愈合为柱状上皮,并且在新上皮中发现了ESMG导管的连续性。在人类和动物中也已注意到ESMGs和导管在损伤后增殖增加。