Yuan Yong, Tong Tie-Jun, Zeng Xiao-Xi, Yang Yu-Shang, Wang Zhi-Qiang, Wang Yun-Cang, Gou Jun-He, Chen Long-Qi
Department of Thoracic Surgery, West China Hospital of Sichuan University, Chengdu 610041, China.
Department of Mathematics, Hong Kong Baptist University, Hong Kong 999077, China.
J Thorac Dis. 2017 Dec;9(12):5249-5260. doi: 10.21037/jtd.2017.11.16.
Esophagectomy with gastric interposition could serve as a good human reflux model to study the molecular pathogenesis of esophageal mucosal damage induced by gastroesophageal reflux. This study was to investigate the role of Notch signaling in reflux injury of esophageal mucosa.
Patients undergoing Ivor-Lewis esophagectomy for early stage esophageal squamous cell carcinoma were included. Follow-ups were scheduled at 6, 18, 36 and 48 months postoperatively, including reflux symptom assessment, endoscopic and histological evaluation of esophageal mucosal damage. The expressions of and its downstream target gene were evaluated by real-time polymerase chain reaction (PCR) and immunohistochemistry (IHC).
Forty-four out of 48 patients completed four follow-ups. Injuries of esophageal remnant confirmed by endoscopical and histological examinations were both more often with a longer postoperative period (P<0.05). The mRNA expression levels of and were decreased in a time-dependent manner after operation (P<0.001). Notch1 and Hes1 mRNA levels were significantly higher in normal squamous mucosa than in esophagitis, and higher in esophagitis than in metaplasia (P<0.05). Immunohistochemical study also demonstrated a similar protein expression pattern. Samples with endoscopic evidence of mucosal damage exhibited lower expression of mRNA levels as compared to biopsies without visualized damage (P=0.035).
This is the first longitudinal study on Notch signaling in human esophagectomy model, our preliminary findings suggest decreased Notch signaling might be involved in the development of mucosa damage caused by gastroesophageal reflux.
胃代食管切除术可作为一种良好的人体反流模型,用于研究胃食管反流所致食管黏膜损伤的分子发病机制。本研究旨在探讨Notch信号通路在食管黏膜反流损伤中的作用。
纳入因早期食管鳞状细胞癌接受Ivor-Lewis食管切除术的患者。术后6、18、36和48个月安排随访,包括反流症状评估、食管黏膜损伤的内镜及组织学评估。通过实时聚合酶链反应(PCR)和免疫组织化学(IHC)评估Notch1及其下游靶基因Hes1的表达。
48例患者中有44例完成了4次随访。内镜及组织学检查证实的食管残余损伤在术后时间较长时更常见(P<0.05)。术后Notch1和Hes1的mRNA表达水平呈时间依赖性下降(P<0.001)。Notch1和Hes1的mRNA水平在正常鳞状黏膜中显著高于食管炎,在食管炎中高于化生(P<0.05)。免疫组织化学研究也显示了类似的蛋白表达模式。与无可见损伤的活检样本相比,有内镜黏膜损伤证据的样本Notch1 mRNA水平表达较低(P=0.035)。
这是在人体食管切除模型中关于Notch信号通路的第一项纵向研究,我们的初步发现表明Notch信号通路减弱可能参与了胃食管反流引起的黏膜损伤的发生发展。