Early-life family structure and microbially induced cancer risk

被引:35
作者
Blaser, Martin J.
Nomura, Abraham
Lee, James
Stemmerman, Grant N.
Perez-Perez, Guillermo I.
机构
[1] NYU, Sch Med, Dept Med, New York, NY USA
[2] NYU, Sch Med, Dept Microbiol, New York, NY 10016 USA
[3] Vet Adm Med Ctr, New York, NY USA
[4] Kuakini Med Ctr, Honolulu, HI USA
[5] Univ Hawaii, Honolulu, HI 96822 USA
[6] Univ Cincinnati, Cincinnati, OH USA
关键词
D O I
10.1371/journal.pmed.0040007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Cancer may follow exposure to an environmental agent after many decades. The bacterium Helicobacter pylori, known to be acquired early in life, increases risk for gastric adenocarcinoma, but other factors are also important. In this study, we considered whether early-life family structure affects the risk of later developing gastric cancer among H. pylori(+) men. Methods and Findings: We examined a long-term cohort of Japanese-American men followed for 28 y, and performed a nested case-control study among those carrying H. pylori or the subset carrying the most virulent cagA(+) H. pylori strains to address whether family structure predicted cancer development. We found that among the men who were H. pylori(+) and/or cagA(+) (it is possible to be cagA(+) and H. pylori(-) if the H. pylori test is falsely negative), belonging to a large sibship or higher birth order was associated with a significantly increased risk of developing gastric adenocarcinoma late in life. For those with cagA(+) strains, the risk of developing gastric cancer was more than twice as high (odds ratio 2.2; 95% confidence interval 1.2-4.0) among those in a sibship of seven or more individuals than in a sibship of between one and three persons. Conclusions: These results provide evidence that early-life social environment plays a significant role in risk of microbially induced malignancies expressing five to eight decades later, and these findings lead to new models to explain these interactions.
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页码:53 / 58
页数:6
相关论文
共 47 条
[1]   CARCINOGENESIS AND AGING [J].
ANISIMOV, VN .
ADVANCES IN CANCER RESEARCH, 1983, 40 :365-424
[2]  
[Anonymous], 1979, Theoretical statistics
[3]   Extensive repetitive DNA facilitates prokaryotic genome plasticity [J].
Aras, RA ;
Kang, J ;
Tschumi, AI ;
Harasaki, Y ;
Blaser, MJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (23) :13579-13584
[4]  
BLASER MJ, 1995, CANCER RES, V55, P562
[5]  
BLASER MJ, 1995, CANCER RES, V55, P2111
[6]   The role of genome diversity and immune evasion in persistent infection with Helicobacter pylori [J].
Cooke, CL ;
Huff, JL ;
Solnick, JV .
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY, 2005, 45 (01) :11-23
[7]  
Danesh J, 1999, ALIMENT PHARM THERAP, V13, P851
[8]   Case-control study of parental age, parity and socioeconomic level in relation to childhood cancers [J].
Dockerty, JD ;
Draper, G ;
Vincent, T ;
Rowan, SD ;
Bunch, KJ .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2001, 30 (06) :1428-1437
[9]   Reliability of Helicobacter pylori and CagA serological assays [J].
Everhart, JE ;
Kruszon-Moran, D ;
Perez-Perez, G .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2002, 9 (02) :412-416
[10]  
Figueiredo C, 2002, J NATL CANCER I, V94, P1680, DOI 10.1093/jnci/94.22.1680