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Axin2 rs2240308 多态性与癌症风险的新概念:一项更新的荟萃分析。

New concept of the Axin2 rs2240308 polymorphism and cancer risk: an updated meta-analysis.

出版信息

Neoplasma. 2017;64(2):269-277. doi: 10.4149/neo_2017_214.

Abstract

Previous meta-analyses reported that the variant T allele of Axin2 rs2240308 is associated with a decreased cancer risk. However, more recent findings have been inconsistent. Therefore, we carried out an updated meta-analysis to examine whether this polymorphism is still associated with a decreased cancer risk. Twelve articles, including 14 case-control studies (2,215 cases and 2,481 controls), were included in our study. Surprisingly, different from previous meta-analyses, no significant association between Axin2 rs2240308 polymorphism and cancer risk was observed (dominant model: OR=0.85; 95% CI=0.68-1.06). In further stratified analyses, rs2240308 was significantly associated with a decreased cancer risk only in Asians (dominant model: OR=0.76; 95% CI=0.66-0.88), while for Caucasians the variant showed no significant association with cancer risk (dominant model: OR=1.09; 95% CI=0.67-1.76). Moreover, the rs2240308 variant exhibited a significant association with a decreased risk of lung cancer and prostate cancer. These findings provided new evidence that differed from previous meta-analyses; Axin2 rs2240308 may not modify general cancer susceptibility. Similar with previous meta-analyses, our analysis indicated that Axin2 rs2240308 may modify cancer susceptibility in an ethnicity- and/or type-specific manner. These findings indicate that further replication studies with large sample sizes are warranted to re-evaluate the relationship between Axin2 rs2240308 and cancer risk, especially in Caucasians.

摘要

先前的荟萃分析报告称,Axin2 rs2240308 中的 T 等位基因变体与癌症风险降低有关。然而,最近的研究结果并不一致。因此,我们进行了一项更新的荟萃分析,以检验这种多态性是否仍然与癌症风险降低有关。我们的研究包括 12 篇文章,其中包括 14 项病例对照研究(2215 例病例和 2481 例对照)。令人惊讶的是,与先前的荟萃分析不同,我们没有观察到 Axin2 rs2240308 多态性与癌症风险之间存在显著关联(显性模型:OR=0.85;95%CI=0.68-1.06)。在进一步的分层分析中,rs2240308 仅与亚洲人群的癌症风险降低显著相关(显性模型:OR=0.76;95%CI=0.66-0.88),而对于高加索人群,该变体与癌症风险无显著关联(显性模型:OR=1.09;95%CI=0.67-1.76)。此外,rs2240308 变体与肺癌和前列腺癌风险降低显著相关。这些发现提供了与先前荟萃分析不同的新证据;Axin2 rs2240308 可能不会改变一般的癌症易感性。与先前的荟萃分析相似,我们的分析表明,Axin2 rs2240308 可能以种族和/或类型特异性的方式影响癌症易感性。这些发现表明,需要进一步进行大规模的复制研究来重新评估 Axin2 rs2240308 与癌症风险之间的关系,尤其是在高加索人群中。

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