Etiology of gastric cancer: What is new?

被引:37
作者
Correa, P
Schneider, BG
机构
[1] Louisiana State Univ, Hlth Sci Ctr, Dept Pathol, New Orleans, LA 70112 USA
[2] Stanley Scott Canc Ctr, New Orleans, LA USA
关键词
D O I
10.1158/1055-9965.EPI-05-0029
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recent advances in understanding of risk factors for gastric cancer have focused attention on genetic polymorphisms in both the human host and in Helicobacter pylori. Variation in genes for cytokines such as interleukin-1 beta and its receptor antagonist may allow identification of those individuals predisposed to mount an immune response that puts them at elevated risk for gastric cancer. Likewise, analysis of how genetic variation in the genome of H. pylori may modulate the action of virulence factors like CagA may prove useful in identification of persons for whom H. pylori eradication efforts would be most important. This review examines recent studies on interleukin-1 beta polymorphisms and H. pylori CagA variation with respect to their modulation of risk for gastric cancer.
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页码:1865 / 1868
页数:4
相关论文
共 54 条
[1]   Determinants and consequences of different levels of CagA phosphorylation for clinical isolates of Helicobacter pylori [J].
Argent, RH ;
Kidd, M ;
Owen, RJ ;
Thomas, RJ ;
Limb, MC ;
Atherton, JC .
GASTROENTEROLOGY, 2004, 127 (02) :514-523
[2]   Helicobacter pylori CagA protein can be tyrosine phosphorylated in gastric epithelial cells [J].
Asahi, M ;
Azuma, T ;
Ito, S ;
Ito, Y ;
Suto, H ;
Nagai, Y ;
Tsubokawa, M ;
Tohyama, Y ;
Maeda, S ;
Omata, M ;
Suzuki, T ;
Sasakawa, C .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 191 (04) :593-602
[3]   Vacuolating cytotoxin (vacA) alleles of Helicobacter pylori comprise two geographically widespread types, m1 and m2, and have evolved through limited recombination [J].
Atherton, JC ;
Sharp, PM ;
Cover, TL ;
Gonzalez-Valencia, G ;
Peek, RM ;
Thompson, SA ;
Hawkey, CJ ;
Blaser, MJ .
CURRENT MICROBIOLOGY, 1999, 39 (04) :211-218
[4]   Implication of the structure of the Helicobacter pylori cag pathogenicity island in induction of interleukin-8 secretion [J].
Audibert, C ;
Burucoa, C ;
Janvier, B ;
Fauchère, JL .
INFECTION AND IMMUNITY, 2001, 69 (03) :1625-1629
[5]   Association between diversity in the Src homology 2 domain-containing tyrosine phosphatase binding site of Helicobacter pylori CagA protein and gastric atrophy and cancer [J].
Azuma, T ;
Yamazaki, S ;
Yamakawa, A ;
Ohtani, M ;
Muramatsu, A ;
Suto, H ;
Ito, Y ;
Dojo, M ;
Yamazaki, Y ;
Kuriyama, M ;
Keida, Y ;
Higashi, H ;
Hatakeyama, M .
JOURNAL OF INFECTIOUS DISEASES, 2004, 189 (05) :820-827
[6]   Translocation of the Helicobacter pylori CagA protein in gastric epithelial cells by a type IV secretion apparatus [J].
Backert, S ;
Ziska, E ;
Brinkmann, V ;
Zimny-Arndt, U ;
Fauconnier, A ;
Jungblut, PR ;
Naumann, M ;
Meyer, TF .
CELLULAR MICROBIOLOGY, 2000, 2 (02) :155-164
[7]   Helicobacter pylori genetic diversity and risk of human disease [J].
Blaser, MJ ;
Berg, DE .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 107 (07) :767-773
[8]  
BLASER MJ, 1995, CANCER RES, V55, P2111
[9]   Comparative analysis of the complete cag pathogenicity island sequence in four Helicobacter pylori isolates [J].
Blomstergren, A ;
Lundin, A ;
Nilsson, C ;
Engstrand, L ;
Lundeberg, J .
GENE, 2004, 328 :85-93
[10]   cag, a pathogenicity island of Helicobacter pylori, encodes type I-specific and disease-associated virulence factors [J].
Censini, S ;
Lange, C ;
Xiang, ZY ;
Crabtree, JE ;
Ghiara, P ;
Borodovsky, M ;
Rappuoli, R ;
Covacci, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (25) :14648-14653