Moghimi Mansour, Ahrar Hossein, Karimi-Zarchi Mojgan, Aghili Kazem, Salari Marjansadat, Zare-Shehneh Masoud, Neamatzadeh Hossein
Department of Pathology, Shahid Sadoughi University of Medical Sciences, Yazd, Iran. Email:
Asian Pac J Cancer Prev. 2018 Dec 25;19(12):3353-3359. doi: 10.31557/APJCP.2018.19.12.3353.
Background: The rs1800871 and rs1800872 polymorphisms of interleukin 10 (IL-10) gene has been indicated to be associated with breast cancer (BC) risk, but study results are still debatable. To derive a more precise evaluation, we performed a comprehensive meta-analysis. Methods: Multiple electronic databases were searched to identify studies assessing the IL-10 rs1800871 and rs1800872 polymorphisms with BC risk. Results: A total of 21 case-control studies with 6054 cases and 6355 controls were included in this met-analysis. There was a significant association between the rs1800871 polymorphism and BC risk (CT vs. TT: OR= 1.17, 95% CI 1.01-1.35, p=0.02; and CC+CT vs. TT: OR= 1.29, 95% CI 1.00-1.66, p=0.04). Moreover, increased BC risks were also associated with the rs1800872 polymorphism (C vs. A: OR= 1.29, 95% CI 1.04-1.60, p=0.01; CC vs. AA: OR= 1.54, 95% CI 1.03-2.30, p=0.03; CC+CA vs. AA: OR= 1.43, 95% CI 1.01-2.01, p=0.03; and CC vs. CA+AA: OR= 1.23, 95% CI 1.01-1.51, p=0.04). A pooling of the studies was also conducted by ethnicity, but failed to show an association of IL-10 rs1800871 and rs1800872 polymorphism with BC risk in Asians and Caucasians. Conclusions: Our results are inconsistent with previous meta-analysis suggests that IL-10 rs1800871 and rs1800872 polymorphisms might contribute to BC susceptibility in overall population, but not by ethnicity.
白细胞介素10(IL-10)基因的rs1800871和rs1800872多态性已被指出与乳腺癌(BC)风险相关,但研究结果仍存在争议。为了得出更精确的评估,我们进行了一项全面的荟萃分析。方法:检索多个电子数据库,以识别评估IL-10 rs1800871和rs1800872多态性与BC风险的研究。结果:本荟萃分析共纳入21项病例对照研究,包括6054例病例和6355例对照。rs1800871多态性与BC风险之间存在显著关联(CT与TT:OR = 1.17,95%CI 1.01 - 1.35,p = 0.02;CC + CT与TT:OR = 1.29,95%CI 1.00 - 1.66,p = 0.04)。此外,BC风险增加也与rs1800872多态性相关(C与A:OR = 1.29,95%CI 1.04 - 1.60,p = 0.01;CC与AA:OR = 1.54,95%CI 1.03 - 2.30,p = 0.03;CC + CA与AA:OR = 1.43,95%CI 1.01 - 2.01,p = 0.03;CC与CA + AA:OR = 1.23,95%CI 1.01 - 1.51,p = 0.04)。还按种族对研究进行了汇总,但未显示IL-10 rs1800871和rs1800872多态性与亚洲人和高加索人中的BC风险存在关联。结论:我们的结果与先前的荟萃分析不一致,表明IL-10 rs1800871和rs1800872多态性可能在总体人群中导致BC易感性,但不受种族影响。