Mozaffari Namin Behrooz, Soltan Dallal Mohammad Mehdi, Ebrahimi Daryani Nasser
Department of Microbiology of Pathobiology, School of Public Health, Tehran University of Medical Sciences, International Campus (TUMS-IC), Tehran, IR Iran; Microbiology and Gut Biology Group, University of Dundee, Ninewells Hospital Medical School, Dundee, UK.
Food Microbiology Research Center, Department of Pathobiology, School of Public Health, Tehran University of Medical Sciences, Tehran, IR Iran; Food Microbiology Research Center, Tehran University of Medical Sciences, Tehran, IR Iran.
Jundishapur J Microbiol. 2015 Dec 26;8(12):e26393. doi: 10.5812/jjm.26393. eCollection 2015 Dec.
Barrett's oesophagus is a pre-malignant condition at gastroesophageal junction in which normal squamous epithelium is replaced by columnar shape epithelium, which predisposes oesophageal adenocarcinoma. It is known that Barrett's oesophagus evolves as a consequence of chronic gastro-oesophageal reflux disease. Although progression of Barrett's oesophagus to adenocarcinoma is still unclear, increasing incidence of oesophageal cancer and mortality worldwide make its study necessary. Several investigations have been made on the aetiology of oesophageal cancer. Most of them assessed genetical or environmental factors. However, potential role of bacteria in the development of oesophageal adenocarcinoma as a new environmental factor has not been addressed. Previous study on Barrett's disease detected presence of Campylobacter concisus as a new emerging pathogen on Barrett's and oesophageal cancer samples compared with healthy individuals. This indicates that this organism might involve in the progression of Barrett's to oesophageal adenocarcinoma.
This study aimed to determine the effects of C. concisus on expression of three biomarkers including interleukin-18 (IL-18), tumour necrosis factor-α (TNF-α) and tumour suppressor gene (p53) in three Barrett's cell lines.
Quantitative real-time PCR assays were developed to measure expression of pro-inflammatory mediators (IL-18 and TNF-α) and gene expression of p53 in Barrett's cell lines in co-culture with C. concisus.
The mentioned organism was able to modulate considerably expression of p53, TNF-α and IL-18 in a time-dependent manner.
The results showed that microorganism influences expression of carcinogenesis biomarker and cytokines in cell line models and possibility promotes oesophageal adenocarcinoma.
巴雷特食管是一种发生于胃食管交界处的癌前病变,正常鳞状上皮被柱状上皮取代,这易引发食管腺癌。已知巴雷特食管是慢性胃食管反流病的结果。尽管巴雷特食管向腺癌的进展仍不明确,但全球食管癌发病率和死亡率的上升使得对其进行研究很有必要。已经对食管癌的病因进行了多项调查。其中大多数评估了遗传或环境因素。然而,细菌作为一种新的环境因素在食管腺癌发生发展中的潜在作用尚未得到探讨。先前关于巴雷特病的研究发现,与健康个体相比,在巴雷特食管和食管癌样本中存在简明弯曲杆菌这一新出现的病原体。这表明这种微生物可能参与了巴雷特食管向食管腺癌的进展。
本研究旨在确定简明弯曲杆菌对三种巴雷特细胞系中三种生物标志物(白细胞介素 -18(IL-18)、肿瘤坏死因子 -α(TNF-α)和肿瘤抑制基因(p53))表达的影响。
开发了定量实时聚合酶链反应检测法,以测量与简明弯曲杆菌共培养的巴雷特细胞系中促炎介质(IL-18和TNF-α)的表达以及p53的基因表达。
上述微生物能够以时间依赖性方式显著调节p53、TNF-α和IL-18的表达。
结果表明,微生物在细胞系模型中影响致癌生物标志物和细胞因子的表达,并可能促进食管腺癌的发生。