Prasad K N, Saxena A, Ghoshal U C, Bhagat M R, Krishnani N
Department of Microbiology.
Department of Microbiology.
Ann Oncol. 2008 Jul;19(7):1299-1303. doi: 10.1093/annonc/mdn055. Epub 2008 Mar 27.
Peroxisome proliferator-activated receptor gamma (PPARgamma) is a ligand-dependent transcription factor involved in various disease processes including inflammation and carcinogenesis. We investigated the association of Pro12Ala PPARgamma polymorphism and Helicobacter pylori infection with gastric cancer and peptic ulcer disease (PUD).
In total, 348 adult patients [62 gastric adenocarcinoma, 45 PUD and 241 nonulcer dyspepsia (NUD)] who underwent an upper gastrointestinal endoscopy were enrolled. PPARgamma polymorphism was analyzed by PCR-based restriction fragment length polymorphism. H. pylori infection was diagnosed by rapid urease test, culture, histopathology and PCR.
PPARgamma G carrier had significant association with gastric adenocarcinoma [P = 0.023, odds ratio (OR) = 2.136, 95% CI = 1.112-4.104] and PUD (P = 0.028, OR = 2.165, 95% CI = 1.008-4.306) when compared with NUD. Combination of G carrier and H. pylori infection further increased the risk of gastric adenocarcinoma (OR = 3.054, 95% CI = 1.195-7.807) and PUD (OR = 11.161, 95% CI = 3.495-35.644). PPARgamma polymorphism did not increase the risk of gastric adenocarcinoma and PUD in H. pylori-negative subjects.
The study suggests that Pro12Ala PPARgamma polymorphism is associated with gastric adenocarcinoma and PUD, and is a potential marker for genetic susceptibility to these two diseases in the presence of H. pylori infection.
过氧化物酶体增殖物激活受体γ(PPARγ)是一种依赖配体的转录因子,参与包括炎症和致癌作用在内的多种疾病过程。我们研究了Pro12Ala PPARγ基因多态性和幽门螺杆菌感染与胃癌及消化性溃疡疾病(PUD)之间的关联。
总共纳入了348例接受上消化道内镜检查的成年患者[62例胃腺癌、45例PUD和241例非溃疡性消化不良(NUD)]。通过基于聚合酶链反应的限制性片段长度多态性分析PPARγ基因多态性。通过快速尿素酶试验、培养、组织病理学和聚合酶链反应诊断幽门螺杆菌感染。
与NUD相比,PPARγ G携带者与胃腺癌[P = 0.023,比值比(OR)= 2.136,95%可信区间(CI)= 1.112 - 4.104]和PUD(P = 0.028,OR = 2.165,95% CI = 1.008 - 4.306)显著相关。G携带者与幽门螺杆菌感染的联合进一步增加了胃腺癌(OR = 3.054,95% CI = 1.195 - 7.807)和PUD(OR = 11.161,95% CI = 3.495 - 35.644)的风险。PPARγ基因多态性在幽门螺杆菌阴性的受试者中未增加胃腺癌和PUD的风险。
该研究表明Pro12Ala PPARγ基因多态性与胃腺癌和PUD相关,并且在存在幽门螺杆菌感染的情况下是这两种疾病遗传易感性的潜在标志物。