Helicobacter pylori CagA protein variation associated with gastric cancer in Asia

被引:85
作者
Azuma, T [1 ]
机构
[1] Univ Fukui, Sch Med, Dept Internal Med 2, Fukui 9101193, Japan
关键词
Helicobacter pylori; CagA; gastric cancer; pathogenicity island; type IV secretion system;
D O I
10.1007/s00535-003-1279-4
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Recent molecular analysis has provided the pathological actions of CagA on gastric epithelial cells. CagA is injected into epithelial cells via the type IV secretion system and undergoes tyrosine phosphorylation in the cells. In addition, translocated CagA forms a physical complex with SHP-2. There are two major CagA subtypes; the East Asian and the Western type. The East Asian CagA protein possesses stronger SHP-2 binding activity than the Western CagA. The grades of inflammation, activity of gastritis, and atrophy are significantly higher in gastritis patients infected with the East Asian CagA-positive strain than in gastritis patients infected with the cagA-negative or Western CagA-positive strains. The prevalence of the East Asian CagA-positive strain is associated with the mortality rate of gastric cancer in Asia. Endemic circulation of H. pylori populations carrying biologically more active CagA proteins in East Asian countries, where the mortality rate of gastric cancer is among the highest in the world, may be involved in increasing the risk of gastric cancer in these populations.
引用
收藏
页码:97 / 103
页数:7
相关论文
共 36 条
[21]  
2-4
[22]   Involvement of an SHP-2-Rho small G protein pathway in hepatocyte growth factor/scatter factor-induced cell scattering [J].
Kodama, A ;
Matozaki, T ;
Fukuhara, A ;
Kikyo, M ;
Ichihashi, M ;
Takai, Y .
MOLECULAR BIOLOGY OF THE CELL, 2000, 11 (08) :2565-2575
[23]  
MARSHALL BJ, 1988, LANCET, V2, P1437
[24]   Translocation of Helicobacter pylori CagA into gastric epithelial cells by type IV secretion [J].
Odenbreit, S ;
Püls, J ;
Sedlmaier, B ;
Gerland, E ;
Fischer, W ;
Haas, R .
SCIENCE, 2000, 287 (5457) :1497-1500
[25]   HELICOBACTER-PYLORI INFECTION AND THE RISK OF GASTRIC-CARCINOMA [J].
PARSONNET, J ;
FRIEDMAN, GD ;
VANDERSTEEN, DP ;
CHANG, Y ;
VOGELMAN, JH ;
ORENTREICH, N ;
SIBLEY, RK .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (16) :1127-1131
[26]   Altered states:: Involvement of phosphorylated CagA in the induction of host cellular growth changes by Helicobacter pylori [J].
Segal, ED ;
Cha, J ;
Lo, J ;
Falkow, S ;
Tompkins, LS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (25) :14559-14564
[27]   Helicobacter pylori attachment to gastric cells induces cytoskeletal rearrangements and tyrosine phosphorylation of host cell proteins [J].
Segal, ED ;
Falkow, S ;
Tompkins, LS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (03) :1259-1264
[28]   Tyrosine phosphorylation of the Helicobacter pylori CagA antigen after cag-driven host cell translocation [J].
Stein, M ;
Rappuoli, R ;
Covacci, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (03) :1263-1268
[29]   The complete genome sequence of the gastric pathogen Helicobacter pylori [J].
Tomb, JF ;
White, O ;
Kerlavage, AR ;
Clayton, RA ;
Sutton, GG ;
Fleischmann, RD ;
Ketchum, KA ;
Klenk, HP ;
Gill, S ;
Dougherty, BA ;
Nelson, K ;
Quackenbush, J ;
Zhou, LX ;
Kirkness, EF ;
Peterson, S ;
Loftus, B ;
Richardson, D ;
Dodson, R ;
Khalak, HG ;
Glodek, A ;
McKenney, K ;
Fitzegerald, LM ;
Lee, N ;
Adams, MD ;
Hickey, EK ;
Berg, DE ;
Gocayne, JD ;
Utterback, TR ;
Peterson, JD ;
Kelley, JM ;
Cotton, MD ;
Weldman, JM ;
Fujii, C ;
Bowman, C ;
Watthey, L ;
Wallin, E ;
Hayes, WS ;
Weidman, JM ;
Fujii, C ;
Borodovsky, M ;
Karp, PD ;
Smith, HO ;
Fraser, CM ;
Venter, JC .
NATURE, 1997, 388 (6642) :539-547
[30]   Geographic distribution of vacA allelic types of Helicobacter pylori [J].
van Doorn, LJ ;
Figueiredo, C ;
Mégraud, F ;
Pena, S ;
Midolo, P ;
Queiroz, DMD .
GASTROENTEROLOGY, 1999, 116 (04) :823-830