Association between diversity in the Src homology 2 domain-containing tyrosine phosphatase binding site of Helicobacter pylori CagA protein and gastric atrophy and cancer

被引:154
作者
Azuma, T [1 ]
Yamazaki, S
Yamakawa, A
Ohtani, M
Muramatsu, A
Suto, H
Ito, Y
Dojo, M
Yamazaki, Y
Kuriyama, M
Keida, Y
Higashi, H
Hatakeyama, M
机构
[1] Fukui Med Univ, Dept Internal Med 2, Matsuoka, Fukui 9101193, Japan
[2] Fukui Med Univ, Dept Endoscop Med, Matsuoka, Fukui 9101193, Japan
[3] Hokkaido Univ, Inst Med Genet, Div Mol Oncol, Sapporo, Hokkaido, Japan
[4] Hokkaido Univ, Grad Sch Sci, Sapporo, Hokkaido, Japan
[5] Okinawa Chubu Hosp, Div Internal Med, Okinawa, Japan
基金
日本学术振兴会;
关键词
D O I
10.1086/381782
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We investigated the relationship between the diversity of Helicobacter pylori CagA protein and clinical outcome. The cagA gene was sequenced in 115 clinical isolates. The binding affinity of CagA to Src homology 2 domain containing tyrosine phosphatase (SHP-2) was examined by in vitro infection. Two major CagA subtypes were observed - the East Asian and the Western type. The grades of inflammation, activity of gastritis, and atrophy were significantly higher in patients with gastritis infected with the East Asian CagA-positive strain than in patients with gastritis infected with cagA-negative or Western CagA-positive strains. All strains isolated from patients with gastric cancer were East Asian CagA positive. East Asian CagA exhibited stronger SHP-2-binding activity than did Western CagA. These findings suggest that infection with East Asian CagA - positive H. pylori is associated with atrophic gastritis and gastric cancer and that persistent active inflammation induced by the East Asian CagA- positive strain may play a role in the pathogenesis of disease.
引用
收藏
页码:820 / 827
页数:8
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