Xia Jun, Sun Rulin
Clinical Laboratory Center, Zhejiang Provincial People's Hospital, Hangzhou, Zhejiang, China (mainland).
People's Hospital of Hangzhou Medical College, Hangzhou, Zhejiang, China (mainland).
Med Sci Monit. 2019 Nov 5;25:8315-8325. doi: 10.12659/MSM.917715.
BACKGROUND Numerous studies have evaluated the relationship between RNASEL gene polymorphisms (rs486907 G>A and rs627928 T>G) and the risk of cancer. However, many of the results have been controversial. To explore the role of RNASEL gene polymorphisms in prostate cancer, we carried out the present meta-analysis. MATERIAL AND METHODS The qualified articles were collected from PubMed, Web of Science, Scopus, CNKI, and WanFang databases to August 2018. A total 23 articles with 40 studies were incorporated into our analysis. RESULTS Our data show that rs486907 was not associated with the risk of prostate cancer in any populations. Nevertheless, rs627928 was reported to promote the development of prostate cancer (T vs. G: OR=1.08, 95% CI=1.01-1.15; TT+TG vs. GG: OR=1.14, 95% CI=1.03-1.25) in allele and recessive models in overall populations. Stratified analyses showed that similar results were obtained in white populations. CONCLUSIONS We report the effect of rs627928 on the development of prostate cancer and confirm that rs486907 is not involved in the risk of prostate cancer in the current meta-analysis. However, research in larger populations is needed to validate our conclusions.
众多研究评估了RNASEL基因多态性(rs486907 G>A和rs627928 T>G)与癌症风险之间的关系。然而,许多结果存在争议。为了探究RNASEL基因多态性在前列腺癌中的作用,我们进行了本次荟萃分析。
从PubMed、Web of Science、Scopus、中国知网和万方数据库收集截至2018年8月的合格文章。总共23篇文章中的40项研究纳入我们的分析。
我们的数据表明,rs486907在任何人群中均与前列腺癌风险无关。然而,据报道,在总体人群的等位基因和隐性模型中,rs627928可促进前列腺癌的发展(T与G相比:OR=1.08,95%CI=1.01-1.15;TT+TG与GG相比:OR=1.14,95%CI=1.03-1.25)。分层分析表明,在白人人群中获得了类似结果。
我们报告了rs627928对前列腺癌发展的影响,并在当前的荟萃分析中证实rs486907与前列腺癌风险无关。然而,需要在更大规模人群中进行研究以验证我们的结论。