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Cumulative Evidence for Association Between IL-8-251T>A and IL-18-607C>A Polymorphisms and Colorectal Cancer Susceptibility: a Systematic Review and Meta-analysis

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JOURNAL OF GASTROINTESTINAL CANCER
卷 52, 期 1, 页码 31-40

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SPRINGER
DOI: 10.1007/s12029-020-00521-w

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Colorectal cancer; Interleukin; Cytokine; Association; Meta-analysis

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The meta-analysis found no significant association between IL-8 -251T>A and IL-18 -607C>A polymorphisms and increased risk of CRC in the global population. Stratified analysis by ethnicity, source of controls, sample size, and Hardy-Weinberg equilibrium (HWE) also showed no significant association between IL-8 -251T>A polymorphism and CRC risk. Further studies with larger sample sizes and diverse ethnicities are recommended to confirm these findings.
Purpose The correlation of IL-8 and IL-18 gene polymorphisms with colorectal cancer (CRC) was investigated by previous studies, though the results remained conflicting. Thus, the meta-analysis was performed to investigate the association of IL-8 -251T>A and IL-18 -607C>A polymorphisms with CRC risk. Methods A comprehensive search of the PubMed, Web of Science, CNKI, SciELO, and Wanfang databases was performed up to February 20, 2020. The strength of the associations was calculated with odds ratios (ORs) and their corresponding 95% of confidence intervals (CIs). Results A total of 16 case-control studies including 13 studies with 3908 cases and 5005 controls on IL-8 -251T>A polymorphism and three studies with 396 cases and 560 controls on IL-18 -607C>A polymorphism were selected. Pooled data revealed that the IL-8 -251T>A and IL-18 -607C>A polymorphisms were not significantly associated with an increased risk of CRC in global population. When stratified by ethnicity, source of controls, sample size, and Hardy-Weinberg equilibrium (HWE), there were still no significant association between IL-8 -251T>A polymorphism and risk of CRC. Conclusions Our results revealed that the IL-8 -251T>A and IL-18 -607C>A polymorphisms were not associated with an increased susceptibility to CRC. We strongly call for further studies with larger sample sizes and different ethnicities to confirm our findings.

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