ASSOCIATION OF MMP-7 -181A>G POLYMORPHISM WITH COLORECTAL CANCER AND GASTRIC CANCER SUSCEPTIBILITY: A SYSTEMATIC REVIEW AND META-ANALYSIS

被引:8
|
作者
Zare, Mohammad [1 ]
Jafari-Nedooshan, Jamal [1 ]
Aghili, Kazem [2 ]
Ahrar, Hossein [2 ]
Jarahzadeh, Mohammad Hossein [3 ]
Seifi-Shalamzari, Neda [4 ]
Zare-Shehneh, Masoud [5 ]
Neamatzadeh, Hossein [5 ]
机构
[1] Shahid Sadoughi Univ Med Sci, Gen Surg, Yazd, Yazd, Iran
[2] Shahid Sadoughi Univ Med Sci, Radiol, Yazd, Yazd, Iran
[3] Shahid Sadoughi Univ Med Sci, Anesthesiol & Crit Care, Yazd, Yazd, Iran
[4] Shahrekord Univ Med Sci, Emergency Med, Yazd, Yazd, Iran
[5] Sadoughi Univ Med Sci, Med Genet, Yazd, Yazd, Iran
关键词
Matrix metalloproteinase-7; Colorectal neoplasms; Stomach neoplasms; Polymorphism; Single nucleotide; Metaanalysis; G-GREATER-THAN; MATRIX-METALLOPROTEINASES; GENE POLYMORPHISMS; INCREASES SUSCEPTIBILITY; RISK; CARCINOMA;
D O I
10.1590/0102-672020190001e1449
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Introduction: The matrix metalloproteinase-7 (MMP-7) gene -181A>G polymorphism has been reported to be associated with colorectal cancer (CRC) and gastric cancer (GC) susceptibility, yet the results of these previous results have been inconsistent or controversial. Aim: To elaborate a meta-analysis to assess the association of -181A>G polymorphism of MMP-7 with CRC and GC risk. Methods: Published literature evaluating the association from PubMed, Web of Science, Google Scholar and other databases were retrieved up to April 25, 2018. Pooled odds ratio (OR) and 95% confidence interval (CI) were calculated using random- or fixed-effects model. Results: A total of 19 case-control studies, which included eleven studies on CRC (2,169 CRC cases and 2,346 controls) and eight studies on GC (1,545 GC cases and 2,366 controls) were identified. There was a significant association between MMP-7 -181A>G polymorphism and GC risk under the homozygote model (GG vs. AA: OR=1.672, 95% CI 1.161-2.409, p=0.006) and the recessive model (GG vs. GA+AA: OR=1.672, 95% CI 1.319-2.554, p=0.001), but not with CRC. By subgroup analysis based on ethnicity, an increased risk of CRC and GC was found only among Asians. Conclusions: This meta-analysis suggests that MMP-7 -181A>G polymorphisms is associated with GC risk, but not with CRC. However, our results clearly showed that the MMP-7 -181A> G polymorphism significantly increased the risk of CRC only in Asians.
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页数:7
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