Murakami K, Fujioka T, Okimoto T, Mitsuishi Y, Oda T, Nishizono A, Nasu M
Second Dept. of Internal Medicine, Oita Medical University, Japan.
Scand J Gastroenterol. 1999 May;34(5):474-7. doi: 10.1080/003655299750026191.
No previous report has shown the relationship between Helicobacter pylori infection and a direct sequence analysis of p53 gene mutation in a biopsy sample of human gastric mucosa.
A total of 60 endoscopic biopsies samples (21 patients with H. pylori-positive gastritis and 9 patients with H. pylori-negative gastritis), including antral mucosa and corpus mucosa, were used in this study. Direct DNA sequencing of exons 5, 6, 7, and 8 of the p53 gene was performed by the dyedeoxy terminator method.
Mutations in the p53 gene were identified in non-hot spot codons in exon 7 and 8 in 11 of 21 samples (52.4%) from H. pylori-positive gastritis patients. There was no mutation in H. pylori-negative gastritis patients.
This finding shows that H. pylori infection can induce p53 point mutations and appears to be involved in the pathway leading to dysplasia or carcinoma.
以往尚无报告显示幽门螺杆菌感染与人类胃黏膜活检样本中p53基因突变的直接序列分析之间的关系。
本研究共使用了60份内镜活检样本(21例幽门螺杆菌阳性胃炎患者和9例幽门螺杆菌阴性胃炎患者),包括胃窦黏膜和胃体黏膜。采用双脱氧终止法对p53基因的第5、6、7和8外显子进行直接DNA测序。
在21份幽门螺杆菌阳性胃炎患者样本中的11份(52.4%)中,第7和8外显子的非热点密码子中发现了p53基因突变。幽门螺杆菌阴性胃炎患者未发现突变。
这一发现表明幽门螺杆菌感染可诱导p53点突变,似乎参与了导致发育异常或癌症的途径。