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遗传变异与幽门螺杆菌感染在胃癌发生中的交互作用

任帅 李倩 朱梦怡 张艳 颜财旺 韦丽琴 靳光付

任帅, 李倩, 朱梦怡, 张艳, 颜财旺, 韦丽琴, 靳光付. 遗传变异与幽门螺杆菌感染在胃癌发生中的交互作用[J]. 中华疾病控制杂志, 2021, 25(9): 1034-1041. doi: 10.16462/j.cnki.zhjbkz.2021.09.008
引用本文: 任帅, 李倩, 朱梦怡, 张艳, 颜财旺, 韦丽琴, 靳光付. 遗传变异与幽门螺杆菌感染在胃癌发生中的交互作用[J]. 中华疾病控制杂志, 2021, 25(9): 1034-1041. doi: 10.16462/j.cnki.zhjbkz.2021.09.008
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

遗传变异与幽门螺杆菌感染在胃癌发生中的交互作用

doi: 10.16462/j.cnki.zhjbkz.2021.09.008
基金项目: 

国家自然科学基金 81872702

国家自然科学基金 82003534

江苏省自然科学基金 BK20200674

详细信息
    通讯作者:

    靳光付,E-mail: guangfujin@njmu.edu.cn

    韦丽琴,E-mail: wlqli1962@163.com

  • 中图分类号: R181.3;R735.2

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

Funds: 

National Natural Science Foundation of China 81872702

National Natural Science Foundation of China 82003534

Natural Science Foundation of Jiangsu Province BK20200674

More Information
  • 摘要:   目的  探讨胃癌已知易感遗传变异与幽门螺杆菌(Helicobacter pylori, H. pylori)在胃癌发生中的交互作用,及其对胃癌发生部位和发病年龄的影响。   方法  采用单纯病例研究设计,在2 426例胃癌患者中,通过二元Logistic回归分析模型分析遗传变异与H. pylori之间的交互作用。   结果  调整混杂因素后发现,遗传变异NSUN 3 rs7624041和DEFB rs2376549与H. pylori感染在胃癌发生中交互作用有统计学意义(OR=1.257,95% CI:1.006~1.571,P=0.044;OR=0.845,95% CI:0.715~0.999,P=0.048)。基于肿瘤部位的分层分析发现,遗传变异与H. pylori感染之间不存在交互作用。基于肿瘤TNM(tumor-node-metastasis)分期的分层分析发现,在TNM早期胃癌患者中,遗传变异lnc-POLR3G-4 rs7712641与H. pylori感染交互作用有统计学意义(OR=1.757,95% CI:1.060~2.915,P=0.029)。基于年龄的分层分析发现,在年龄 < 60岁人群中,ASHIL rs80142782、NSUN 3 rs7624041和DEFB rs2376549与H. pylori感染交互作用有统计学意义(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);而在年龄≥60岁人群中,仅有PSCA rs2294008和CUX 2 rs6490061与H. pylori感染交互作用有统计学意义(OR=0.775,95% CI:0.630~0.954,P=0.016;OR=0.790,95% CI:0.635~0.982,P=0.034)。   结论  胃癌的发生发展较为复杂,通过整合遗传因素和环境因素,针对易感高危人群采取H. pylori的根除措施,将有助于预防胃癌的发生发展。
  • 表  1  研究对象基本信息[n(%)]

    Table  1.   Baseline information of participants [n(%)]

    变量 例数 H. pylori阳性(n=1 344) H. pylori阴性(n=1 082) χ2
    性别 1.745
      男 1 814 1 019(75.8) 795(73.5)
      女 612 325(24.2) 287(26.5)
    吸烟 3.224
      是 807 472(36.8) 335(33.2)
      否 1 482 809(63.2) 673(66.8)
    饮酒 1.630
      是 680 395(30.9) 285(28.4)
      否 1 600 883(69.1) 717(71.6)
    肿瘤部位 0.663
      非贲门 1 009 570(60.3) 439(58.3)
      贲门 690 376(39.7) 314(41.7)
    TNM分期 4.823
      早期 347 202(39.8) 145(32.9)
      晚期 602 306(60.2) 296(67.1)
    下载: 导出CSV

    表  2  遗传变异与H. pylori的交互作用[n(%)]

    Table  2.   Interaction between genetic variation and H. pylori [n(%)]

    染色体及遗传变异 H. pylori阳性(n=1 344) H. pylori阴性(n=1 082) OR(95% CI)值 a P 染色体及遗传变异 H. pylori阳性(n=1 344) H. pylori阴性(n=1 082) OR(95% CI)值a P
    1q22 6p22.1
      MUCI rs4072037   BTN 3A 2 rs 1679709
        CT+CC 330(24.6) 290(26.8) 1.000     AG+AA 354(26.3) 305(28.2) 1.000
        TT 1014(75.4) 792(73.2) 1.123(0.929~1.358) 0.229     GG 990(73.7) 777(71.8) 1.096(0.910~1.321) 0.334
    1q22 6p21.1
      ASHIL rs 80142782   UNC 5CL, TSPO 2 rs 2294693
        CT+CC 145(10.8) 135(12.5) 1.000     TT 800(59.5) 613(56.7) 1.000
        TT 1 199(89.2) 947(87.5) 1.213(0.938~1.568) 0.141     CT+CC 544(40.5) 469(43.3) 0.912(0.770~1.079) 0.282
    3q11.2 8q24.3
      NSUN 3 rs7624041   PSCA rs2294008
        AA 1 096(81.5) 911(84.2) 1.000     CC 677(50.4) 516(47.7) 1.000
        AG+GG 248(18.5) 171(15.8) 1.257(1.006~1.571) 0.044     CT+TT 667(49.6) 566(52.3) 0.875(0.741~1.033) 0.115
    3q13.31 9q34.2
      ZBTB20 rs9841504   ABO rs7849280
        CG+GG 338(25.1) 265(24.5) 1.000     AG+GG 550(40.9) 459(42.4) 1.000
        CC 1 006(74.9) 817(75.5) 1.023(0.844~1.242) 0.814     AA 794(59.1) 623(57.6) 1.084(0.916~1.283) 0.347
    4q28.1 10q23.33
      LOC285419, ANKRD50 rs 10029005   PLCE 1, KIAA 1516 rs 2274223
        GG 571(42.5) 436(40.3) 1.000     AA 720(53.6) 545(50.4) 1.000
        AG+AA 773(57.5) 646(59.7) 0.913(0.772~1.081) 0.293     AG+GG 624(46.4) 537(49.6) 0.928(0.786~1.096) 0.380
    5p13.1 12q24.11-12
      PRKAA 1 rs 1 3361707   CUX 2 rs6490061
        TT 281(20.9) 239(22.1) 1.000     CC 525(39.1) 415(38.4) 1.000
        CT+CC 1 063(79.1) 843(77.9) 1.083(0.886~1.325) 0.437     CT+TT 819(60.9) 667(61.6) 0.954(0.804~1.132) 0.592
    5q14.3 20q11.21
      lnc-POLR3G-4 rs7712641   DEFB家族rs2376549
        CT+TT 950(70.7) 773(71.4) 1.000     TT 773(57.5) 578(53.4) 1.000
        CC 394(29.3) 309(28.6) 1.021(0.851~1.226) 0.821     CT+CC 571(42.5) 504(46.6) 0.845(0.715~0.999) 0.048
    注:a调整年龄、性别、吸烟以及饮酒。
    下载: 导出CSV

    表  3  不同TNM分期中遗传变异与H. pylori对胃癌发生的交互作用[n(%)]

    Table  3.   Interaction between genetic variation and H. pylori infection in different TNM stages of gastric cancer [n(%)]

    染色体及遗传变异 TNM早期(N=347) TNM晚期(N=602)
    H. pylori阳性(n=202) H. pylori阴性(n=145) OR(95% CI)值 a P H. pylori阳性(n=306) H. pylori阴性(n=296) OR(95% CI)值 a P
    1q22
      MUCI rs4072037
        CT+CC 46(22.8) 39(26.9) 1.000 75(24.5) 68(23.0) 1.000
        TT 156(77.2) 106(73.1) 1.331(0.797~2.224) 0.275 231(75.5) 228(77.0) 0.834(0.563~1.237) 0.367
    1q22
      ASHIL rs80142782
        CT+CC 23(11.4) 17(11.7) 1.000 30(9.8) 38(12.8) 1.000
        TT 179(88.6) 128(88.3) 1.128(0.569~2.234) 0.731 276(90.2) 258(87.2) 1.254(0.735~2.142) 0.406
    3q11.2
      NSUN 3 rs7624041
        AA 166(82.2) 128(88.3) 1.000 254(83.0) 248(83.8) 1.000
        AG+GG 36(17.8) 17(11.7) 1.539(0.796~2.974) 0.200 52(17.0) 48(16.2) 1.104(0.707~1.723) 0.664
    3q13.31
      ZBTB 20 rs9841504
        CG+GG 55(27.2) 34(23.4) 1.000 85(27.8) 76(25.7) 1.000
        CC 147(72.8) 111(76.6) 0.847(0.507~1.415) 0.527 221(72.2) 220(74.3) 1.005(0.690~1.466) 0.978
    4q28.1
      LOC 285419, ANKRD 50 rs10029005
        GG 90(44.6) 54(37.2) 1.000 136(44.4) 122(41.2) 1.000
        AG+AA 112(55.4) 91(62.8) 0.742(0.470~1.172) 0.201 170(55.6) 174(58.8) 0.882(0.630~1.233) 0.462
    5p13.1
      PRKAA 1 rs13361707
        TT 43(21.3) 28(19.3) 1.000 70(22.9) 65(22.0) 1.000
        CT+CC 159(78.7) 117(80.7) 0.902(0.517~1.574) 0.716 236(77.1) 231(78.0) 0.922(0.619~1.371) 0.687
    5q14.3
      lnc-POLR3G-4 rs7712641
        CT+TT 132(65.3) 112(77.2) 1.000 224(73.2) 222(75.0) 1.000
        CC 70(34.7) 33(22.8) 1.757(1.060~2.915) 0.029 82(26.8) 74(25.0) 1.093(0.748~1.597) 0.647
    6p22.1
      BTN 3A 2 rs1679709
        AG+AA 50(24.8) 37(25.5) 1.000 94(30.7) 79(26.7) 1.000
        GG 152(75.2) 108(74.5) 1.083(0.647~1.812) 0.762 212(69.3) 217(73.3) 0.840(0.583~1.209) 0.347
    6p21.1
      UNC 5CL, TSPO 2 rs2294693
        TT 128(63.4) 89(61.4) 1.000 174(56.9) 163(55.1) 1.000
        CT+CC 74(36.6) 56(38.6) 0.973(0.611~1.550) 0.909 132(43.1) 133(44.9) 0.998(0.715~1.392) 0.990
    8q24.3
      PSCA rs2294008
        CC 102(50.5) 80(55.2) 1.000 156(51.0) 144(48.6) 1.000
        CT+TT 100(49.5) 65(44.8) 1.147(0.732~1.795) 0.550 150(49.0) 152(51.4) 0.926(0.663~1.292) 0.650
    9q34.2
      ABO rs7849280
        AG+GG 85(42.1) 63(43.4) 1.000 117(38.2) 124(41.9) 1.000
        AA 117(57.9) 82(56.6) 1.097(0.698~1.723) 0.688 189(61.8) 172(58.1) 1.135(0.809~1.592) 0.464
    10q23.33
      PLCE 1, KIAA 1516 rs2274223
        AA 109(54.0) 72(49.7) 1.000 168(54.9) 147(49.7) 1.000
        AG+GG 93(46.0) 73(50.3) 0.853(0.543~1.340) 0.490 138(45.1) 149(50.3) 0.883(0.632~1.234) 0.466
    12q24.11-12
      CUX 2 rs6490061
        CC 77(38.1) 72(49.7) 1.000 117(38.2) 118(39.9) 1.000
        CT+TT 125(61.9) 73(50.3) 1.478(0.940~2.323) 0.090 189(61.8) 178(60.1) 1.061(0.754~1.492) 0.735
    20q11.21
      DEFB家族rs2376549
        TT 117(57.9) 80(55.2) 1.000 161(52.6) 152(51.4) 1.000
        CT+CC 85(42.1) 65(44.8) 1.005(0.640~1.578) 0.983 145(47.4) 144(48.6) 0.954(0.685~1.329) 0.780
    注:a调整年龄、性别、吸烟以及饮酒。
    下载: 导出CSV

    表  4  不同发病年龄中遗传变异与H. pylori对胃癌发生的交互作用[n(%)]

    Table  4.   Interaction between genetic variation and H. pylori infection in different age groups of gastric cancer [n(%)]

    染色体及遗传变异 发病年龄 < 60岁(N=872) 发病年龄≥60岁(N=1 554)
    H. pylori阳性(n=485) H. pylori阴性(n=387) OR(95% CI)值 a P H. pylori阳性(n=859) H. pylori阴性(n=695) OR(95% CI)值 a P
    1q22
      MUCI rs4072037
        CT+CC 101(20.8) 101(26.1) 1.000 229(26.7) 189(27.2) 1.000
        TT 384(79.2) 286(73.9) 1.291(0.930~1.793) 0.127 630(73.3) 506(72.8) 1.053(0.835~1.329) 0.662
    1q22
      ASHIL rs80142782
        CT+CC 38(7.8) 47(12.1) 1.000 107(12.5) 88(12.7) 1.000
        TT 447(92.2) 340(87.9) 1.602(1.006~2.551) 0.047 752(87.5) 607(87.3) 1.079(0.792~1.470) 0.630
    3q11.2
      NSUN 3 rs7624041
        AA 379(78.1) 333(86.0) 1.000 717(83.5) 578(83.2) 1.000
        AG+GG 106(21.9) 54(14.0) 1.811(1.247~2.632) 0.002 142(16.5) 117(16.8) 1.018(0.769~1.348) 0.901
    3q13.31
      ZBTB20 rs9841504
        CG+GG 110(22.7) 85(22.0) 1.000 228(26.5) 180(25.9) 1.000
        CC 375(77.3) 302(78.0) 0.988(0.704~1.388) 0.946 631(73.5) 515(74.1) 1.037(0.819~1.313) 0.762
    4q28.1
      LOC285419, ANKRD50 rs10029005
        GG 213(43.9) 147(38.0) 1.000 358(41.7) 289(41.6) 1.000
        AG+AA 272(56.1) 240(62.0) 0.774(0.582~1.029) 0.078 501(58.3) 406(58.4) 1.008(0.817~1.244) 0.939
    5p13.1
      PRKAA1 rs13361707
        TT 98(20.2) 91(23.5) 1.000 183(21.3) 148(21.3) 1.000
        CT+CC 387(79.8) 296(76.5) 1.230(0.879~1.722) 0.227 676(78.7) 547(78.7) 1.017(0.790~1.309) 0.895
    5q14.3
      lnc-POLR3G-4 rs7712641
        CT+TT 337(69.5) 276(71.3) 1.000 613(71.4) 497(71.5) 1.000
        CC 148(30.5) 111(28.7) 1.009(0.746~1.367) 0.952 246(28.6) 198(28.5) 1.035(0.823~1.301) 0.771
    6p22.1
      BTN 3A 2 rs1679709
        AG+AA 121(24.9) 106(27.4) 1.000 233(27.1) 199(28.6) 1.000
        GG 364(75.1) 281(72.6) 1.168(0.850~1.605) 0.338 626(72.9) 496(71.4) 1.055(0.837~1.329) 0.649
    6p21.1
      UNC 5CL, TSPO 2 rs2294693
        TT 286(59.0) 220(56.8) 1.000 514(59.8) 393(56.5) 1.000
        CT+CC 199(41.0) 167(43.2) 0.929(0.701~1.232) 0.611 345(40.2) 302(43.5) 0.902(0.730~1.113) 0.335
    8q24.3
      PSCA rs2294008
        CC 216(44.5) 186(48.1) 1.000 461(53.7) 330(47.5) 1.000
        CT+TT 269(55.5) 201(51.9) 1.098(0.831~1.450) 0.512 398(46.3) 365(52.5) 0.775(0.630~0.954) 0.016
    9q34.2
      ABO rs7849280
        AG+GG 224(46.2) 171(44.2) 1.000 326(38.0) 288(41.4) 1.000
        AA 261(53.8) 216(55.8) 0.936(0.708~1.238) 0.644 533(62.0) 407(58.6) 1.181(0.956~1.459) 0.123
    10q23.33
      PLCE 1, KIAA 1516 rs2274223
        AA 259(53.4) 198(51.2) 1.000 461(53.7) 347(49.9) 1.000
        AG+GG 226(46.6) 189(48.8) 0.954(0.722~1.261) 0.742 398(46.3) 348(50.1) 0.912(0.741~1.123) 0.386
    12q24.11-12
      CUX 2 rs6490061
        CC 195(40.2) 178(46.0) 1.000 330(38.4) 237(34.1) 1.000
        CT+TT 290(59.8) 209(54.0) 1.297(0.980~1.717) 0.069 529(61.6) 458(65.9) 0.790(0.635~0.982) 0.034
    20q11.21
      DEFB家族rs2376549
        TT 281(57.9) 197(50.9) 1.000 492(57.3) 381(54.8) 1.000
        CT+CC 204(42.1) 190(49.1) 0.688(0.520~0.910) 0.009 367(42.7) 314(45.2) 0.954(0.774~1.176) 0.660
    注:a调整年龄、性别、吸烟以及饮酒。
    下载: 导出CSV
  • [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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出版历程
  • 收稿日期:  2021-02-06
  • 修回日期:  2021-03-23
  • 网络出版日期:  2021-10-23
  • 刊出日期:  2021-09-10

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