Genetic polymorphisms in the cag pathogenicity island of Helicobacter pylori and risk of stomach cancer and high-grade premalignant gastric lesions

被引:21
作者
Canzian, Federico [1 ]
Rizzato, Cosmeri [2 ]
Obazee, Ofure [1 ]
Stein, Angelika [1 ]
Flores-Luna, Lourdes [3 ]
Camorlinga-Ponce, Margarita [4 ]
Mendez-Tenorio, Alfonso [5 ]
Vivas, Jorge [6 ]
Trujillo, Esperanza [7 ]
Jang, Hyejong [8 ]
Chen, Wei [8 ]
Kasamatsu, Elena [9 ]
Mercedes Bravo, Maria [7 ]
Torres, Javier [4 ]
Munoz, Nubia [10 ]
Kato, Ikuko [8 ]
机构
[1] German Canc Res Ctr, Genom Epidemiol Grp, D-69120 Heidelberg, Germany
[2] Univ Pisa, Dept Translat Res & New Technol Med & Surg, Pisa, Italy
[3] Natl Inst Publ Hlth, Ctr Publ Hlth Res, Cuernavaca, Morelos, Mexico
[4] Inst Mexicano Seguro Social, UMAE Pediat, Unidad Invest Enfermedades Infecciosas, Mexico City, DF, Mexico
[5] Inst Politecn Nacl, ENCB, Lab Biotecnol & Bioinformat Genom, Mexico City, DF, Mexico
[6] Canc Control Ctr Tachira State, San Cristobal, Venezuela
[7] Inst Nacl Cancerol, Grp Invest Biol Canc, Bogota, Colombia
[8] Wayne State Univ, Sch Med, Dept Oncol, Detroit, MI USA
[9] Natl Univ Asuncion, Inst Invest Ciencias Salud, Asuncion, Paraguay
[10] Canc Inst Colombia, Bogota, Colombia
基金
美国国家卫生研究院;
关键词
gastric cancer; genetic polymorphisms; Helicobacter pylori; pathogenicity island; premalignant gastric lesions; PRECANCEROUS LESIONS; INFECTION; ASSOCIATION; PREVALENCE; PROTEIN; DISPLACEMENT; DIVERSITY; WORLDWIDE; DISEASE; SYSTEM;
D O I
10.1002/ijc.33032
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Helicobacter pylori (Hp) infects the stomach of about half of the human population and is strongly associated with the risk of gastric cancer (GC) and its premalignant precursors. The cag pathogenicity island (cagPAI) is a region of the Hp genome encoding for key molecular machinery involved in the infection process. Following a sequencing study, we selected 50 genetic polymorphisms located in seven cagPAI genes and tested their associations with the risk of advanced gastric premalignant lesions and GC in 1220 subjects from various Latin American populations showing the whole spectrum of phenotypes from gastritis to GC. We found that three polymorphisms of cagA are associated with the risk of advanced gastric premalignant lesions (incomplete intestinal metaplasia [ie, Type 2 and 3] or dysplasia), and that six polymorphisms located in cagA, cagL and cagI were associated with risk of GC. When corrected for multiple testing none of the associations were statistically significant. However, scores built by integrating the individual polymorphisms were significantly associated with the risk of advanced gastric premalignant lesions and GC. These results have the potential of establishing markers for risk stratification in the general population, in view of targeting Hp eradication to high-risk population groups.
引用
收藏
页码:2437 / 2445
页数:9
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