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CN 34-1304/RISSN 1674-3679

Volume 25 Issue 9
Oct.  2021
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Article Contents
REN Shuai, Li Qian, ZHU Meng-yi, ZHANG Yan, YAN Cai-wang, WEI Li-qin, JIN Guang-fu. Interaction between genetic variation and Helicobacter pylori infection in the occurrence of gastric cancer[J]. CHINESE JOURNAL OF DISEASE CONTROL & PREVENTION, 2021, 25(9): 1034-1041. doi: 10.16462/j.cnki.zhjbkz.2021.09.008
Citation: REN Shuai, Li Qian, ZHU Meng-yi, ZHANG Yan, YAN Cai-wang, WEI Li-qin, JIN Guang-fu. Interaction between genetic variation and Helicobacter pylori infection in the occurrence of gastric cancer[J]. CHINESE JOURNAL OF DISEASE CONTROL & PREVENTION, 2021, 25(9): 1034-1041. doi: 10.16462/j.cnki.zhjbkz.2021.09.008

Interaction between genetic variation and Helicobacter pylori infection in the occurrence of gastric cancer

doi: 10.16462/j.cnki.zhjbkz.2021.09.008
Funds:

National Natural Science Foundation of China 81872702

National Natural Science Foundation of China 82003534

Natural Science Foundation of Jiangsu Province BK20200674

More Information
  • Corresponding author: WEI Li-qin,E-mail: wlqli1962@163.com; JIN Guang-fu,E-mail: guangfujin@njmu.edu.cn
  • Received Date: 2021-02-06
  • Rev Recd Date: 2021-03-23
  • Available Online: 2021-10-23
  • Publish Date: 2021-09-10
  •   Objective  To investigate the interaction between known genetic variation of gastric cancer and Helicobacter pylori (H. pylori) in the occurrence of gastric cancer, and its effect on tumor site and the age at onset of gastric cancer.   Methods  With a case-only design, the interaction between genetic variation and H. pylori was analyzed by binary Logistic regression analysis in 2 426 patients with gastric cancer.   Results  After adjusting confounding factors, the interactions of genetic variation NSUN 3 rs7624041 and DEFB rs 2376549 with H. pylori infection in gastric cancer were statistically significant (OR=1.257, 95% CI: 1.006-1.571, P=0.044; OR=0.845, 95% CI: 0.715-0.999, P=0.048). Based on the hierarchical analysis of tumor location, there was no interaction between genetic variation and H. pylori infection. Hierarchical analysis based on tumor stage showed that the interaction between lnc-POLR3G-4 rs7712641 and H. pylori infection was statistically significant in patient with early gastric cancer (OR=1.757, 95% CI: 1.060-2.915, P=0.029). The age-based stratified analysis results showed that the interactions between ASHIL rs80142782, NSUN 3 rs7624041, DEFB rs2376549 and H. pylori infection were statistically significant in people aged < 60 years (OR=1.602, 95% CI: 1.006-2.551, P=0.047; OR=1.811, 95% CI: 1.247-2.632, P=0.002; OR=0.688, 95% CI: 0.520-0.910, P=0.009). And the interactions between PSCA rs2294008, CUX 2 rs6490061 and H. pylori infection were statistically significant in people over 60 years old (OR=0.775, 95% CI: 0.630-0.954, P=0.016; OR=0.790, 95% CI: 0.635-0.982, P=0.034).   Conclusions  The occurrence and development of gastric cancer is complex. It is helpful to prevent the occurrence and development of gastric cancer by integrating genetic factors and environmental factors and taking targeted H. pylori eradication measures for susceptible and high-risk groups.
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  • [1]
    Bray F, Ferlay J, Soerjomataram I, et al. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries[J]. CA Cancer J Clin, 2018, 68(6): 394-424. DOI: 10.3322/caac.21492.
    [2]
    Ferlay J, Shin HR, Bray F, et al. Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008[J]. Int J Cancer, 2010, 127(12): 2893-2917. DOI: 10.1002/ijc.25516.
    [3]
    Torre LA, Bray F, Siegel RL, et al. Global cancer statistics, 2012[J]. CA Cancer J Clin, 2015, 65(2): 87-108. DOI: 10.3322/caac.21262.
    [4]
    Jemal A, Miller KD, Ma JM, et al. Higher lung cancer incidence in young women than young men in the United States[J]. N Engl J Med, 2018, 378(21): 1999-2009. DOI: 10.1056/NEJMoa1715907.
    [5]
    Soerjomataram I, Lortet-Tieulent J, Parkin DM, et al. Global burden of cancer in 2008: a systematic analysis of disability-adjusted life-years in 12 world regions[J]. Lancet, 2012, 380(9856): 1840-1850. DOI: 10.1016/S0140-6736(12)60919-2.
    [6]
    Study Group of Millennium Genome Project for Cancer, Sakamoto H, Yoshimura K, et al. Genetic variation in PSCA is associated with susceptibility to diffuse-type gastric cancer[J]. Nat Genet, 2008, 40(6): 730-740. DOI: 10.1038/ng.152.
    [7]
    Abnet CC, Freedman ND, Hu N, et al. A shared susceptibility locus in PLCE 1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma[J]. Nat Genet, 2010, 42(9): 764-767. DOI: 10.1038/ng.649.
    [8]
    Wang LD, Zhou FY, Li XM, et al. Genome-wide association study of esophageal squamous cell carcinoma in Chinese subjects identifies susceptibility loci at PLCE 1 and C20orf54[J]. Nat Genet, 2010, 42(9): 759-763. DOI: 10.1038/ng.648.
    [9]
    Shi YY, Hu ZB, Wu C, et al. A genome-wide association study identifies new susceptibility loci for non-cardia gastric cancer at 3q13.31 and 5p13.1[J]. Nat Genet, 2011, 43(12): 1215-1218. DOI: 10.1038/ng.978.
    [10]
    Hu N, Wang Z, Song X, et al. Genome-wide association study of gastric adenocarcinoma in Asia: a comparison of associations between cardia and non-cardia tumours[J]. Gut, 2016, 65(10): 1611-1618. DOI: 10.1136/gutjnl-2015-309340.
    [11]
    Wang ZM, Dai JC, Hu N, et al. Identification of new susceptibility loci for gastric non-cardia adenocarcinoma: pooled results from two Chinese genome-wide association studies[J]. Gut, 2017, 66(4): 581-587. DOI: 10.1136/gutjnl-2015-310612.
    [12]
    Zhu M, Yan C, Ren C, et al. Exome array analysis identifies variants in SPOCD1 and BTN 3A 2 that affect risk for gastric cancer[J]. Gastroenterology, 2017, 152(8): 2011-2021. DOI: 10.1053/j.gastro.2017.02.017.
    [13]
    Tanikawa C, Kamatani Y, Toyoshima O, et al. Genome-wide association study identifies gastric cancer susceptibility loci at 12q24.11-12 and 20q11.21[J]. Cancer Sci, 2018, 109(12): 4015-4024. DOI: 10.1111/cas.13815.
    [14]
    Yan C, Zhu M, Ding Y, et al. Meta-analysis of genome-wide association studies and functional assays decipher susceptibility genes for gastric cancer in Chinese populations[J]. Gut, 2020, 69(4): 641-651. DOI: 10.1136/gutjnl-2019-318760.
    [15]
    Hooi JKY, Lai WY, Ng WK, et al. Global prevalence of Helicobacter pylori infection: systematic review and meta-analysis[J]. Gastroenterology, 2017, 153(2): 420-429. DOI: 10.1053/j.gastro.2017.04.022.
    [16]
    Cai M, Dai SY, Chen WQ, et al. Environmental factors, seven GWAS-identified susceptibility loci, and risk of gastric cancer and its precursors in a Chinese population[J]. Cancer Med, 2017, 6(3): 708-720. DOI: 10.1002/cam4.1038.
    [17]
    Lindén SK, Sheng YH, Every AL, et al. MUC1 limits Helicobacter pylori infection both by steric hindrance and by acting as a releasable decoy[J]. PLoS Pathog, 2009, 5(10): e1000617. DOI: 10.1371/journal.ppat.1000617.
    [18]
    Piegorsch WW, Weinberg CR, Taylor JA. Non-hierarchical Logistic models and case-only designs for assessing susceptibility in population-based case-control studies[J]. Stat Med, 1994, 13(2): 153-162. DOI: 10.1002/sim.4780130206.
    [19]
    易洪刚, 陈峰. 单纯病例研究[J]. 国外医学(流行病学传染病学分册), 2004, 31(1): 60-62. DOI: 10.3760/cma.j.issn.1673-4149.2004.01.020.

    Yi HG, Chen F. Case-only study[J]. Foreign Med Sci Epidemiol Lemology Fascicle, 2004, 31(1): 60-62. DOI: 10.3760/cma.j.issn.1673-4149.2004.01.020.
    [20]
    Khoury MJ, Flanders WD. Nontraditional epidemiologic approaches in the analysis of gene-environment interaction: case-control studies with no controls![J]. Am J Epidemiol, 1996, 144(3): 207-213. DOI: 10.1093/oxfordjournals.aje.a008915.
    [21]
    Amin MB, Edge S, Greene F, et al. AJCC cancer staging manual[M]. 8th ed. New York: Springer, 2017.
    [22]
    Amirian ES, Scheurer ME, Liu YH, et al. A novel approach to exploring potential interactions among single-nucleotide polymorphisms of inflammation genes in gliomagenesis: an exploratory case-only study[J]. Cancer Epidemiol Biomarkers Prev, 2011, 20(8): 1683-1689. DOI: 10.1158/1055-9965.EPI-11-0203.
    [23]
    Zhai RH, Zhao Y, Liu G, et al. Interactions between environmental factors and polymorphisms in angiogenesis pathway genes in esophageal adenocarcinoma risk: a case-only study[J]. Cancer, 2012, 118(3): 804-811. DOI: 10.1002/cncr.26325.
    [24]
    Zeng ZR, Wu XQ, Chen FG, et al. Polymorphisms in prostate stem cell antigen gene rs2294008 increase gastric cancer risk in Chinese[J]. Mol Carcinog, 2011, 50(5): 353-358. DOI: 10.1002/mc.20718.
    [25]
    Lochhead P, Frank B, Hold GL, et al. Genetic variation in the prostate stem cell antigen gene and upper gastrointestinal cancer in white individuals[J]. Gastroenterology, 2011, 140(2): 435-441. DOI: 10.1053/j.gastro.2010.11.001.
    [26]
    Machida-Montani A, Sasazuki S, Inoue M, et al. Association of Helicobacter pylori infection and environmental factors in non-cardia gastric cancer in Japan[J]. Gastric Cancer, 2004, 7(1): 46-53. DOI: 10.1007/s10120-004-0268-5.
    [27]
    李鑫, 李武良, 李萍. 幽门螺杆菌感染与TNM胃癌分期相关性的研究[J]. 现代消化及介入诊疗, 2018, 23(1): 11-14. DOI: 10.3969/j.issn.1672-2159.2018.01.003.

    Li X, Li WL, Li P. Relationship between Helicobacter pylori infection and TNM stages of gastric cancer[J]. Mod Dig Interv, 2018, 23(1): 11-14. DOI: 10.3969/j.issn.1672-2159.2018.01.003.
    [28]
    Caruso ML, Fucci L. Histological identification of Helicobacter pylori in early and advanced gastric cancer[J]. J Clin Gastroenterol, 1990, 12(5): 601-602. http://www.ncbi.nlm.nih.gov/pubmed/2103734
    [29]
    Tang YL, Gan RL, Dong BH, et al. Detection and location of Helicobacter pylori in human gastric carcinomas[J]. World J Gastroenterol, 2005, 11(9): 1387-1391. DOI: 10.3748/wjg.v11.i9.1387.
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