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AURKA基因rs2273535位点T>A多态性与癌症风险的关联:一项荟萃分析的系统评价

AURKA rs2273535 T>A Polymorphism Associated With Cancer Risk: A Systematic Review With Meta-Analysis.

作者信息

Wang Shujie, Qi Jian, Zhu Meiling, Wang Meng, Nie Jinfu

机构信息

Anhui Province Key Laboratory of Medical Physics and Technology, Center of Medical Physics and Technology, Hefei Institutes of Physical Science, Chinese Academy of Sciences, Hefei, China.

Hefei Cancer Hospital, Chinese Academy of Sciences, Hefei, China.

出版信息

Front Oncol. 2020 Jun 30;10:1040. doi: 10.3389/fonc.2020.01040. eCollection 2020.

Abstract

Aurora kinase A (AURKA) is a cell cycle regulatory serine/threonine kinase that promotes cell cycle progression. It plays an important role in regulating the transition from G2 to M phase during mitosis. The association between the AURKA rs2273535 T>A polymorphism and cancer risk has been investigated, but the results remain inconsistent. To get a more accurate conclusion, we conducted a comprehensive meta-analysis of 36 case-control studies, involving 22,884 cancer cases and 30,497 healthy controls. Crude odds ratios (ORs) and 95% confidence intervals (CIs) were calculated to determine the association of interest. Pooled analysis indicated that the AURKA rs2273535 T>A polymorphism increased the overall risk of cancer (homozygous: OR = 1.17, 95% CI = 1.04-1.33; recessive: OR = 1.15, 95% CI = 1.05-1.25; allele: OR = 1.07, 95% CI = 1.02-1.13). Stratification analysis by cancer type further showed that this polymorphism was associated with an increased breast cancer risk. This meta-analysis indicated that the AURKA rs2273535 T>A polymorphism was associated with an overall increased cancer risk, especially breast cancer. Further validation experiments are needed to strengthen our conclusion.

摘要

极光激酶A(AURKA)是一种细胞周期调节性丝氨酸/苏氨酸激酶,可促进细胞周期进程。它在有丝分裂过程中调节从G2期到M期的转变中发挥重要作用。人们已经对AURKA rs2273535 T>A多态性与癌症风险之间的关联进行了研究,但结果仍不一致。为了得出更准确的结论,我们对36项病例对照研究进行了全面的荟萃分析,涉及22884例癌症病例和30497例健康对照。计算了粗比值比(OR)和95%置信区间(CI)以确定感兴趣的关联。汇总分析表明,AURKA rs2273535 T>A多态性增加了癌症的总体风险(纯合子:OR = 1.17,95% CI = 1.04-1.33;隐性:OR = 1.15,95% CI = 1.05-1.25;等位基因:OR = 1.07,95% CI = 1.02-1.13)。按癌症类型进行的分层分析进一步表明,这种多态性与乳腺癌风险增加有关。这项荟萃分析表明,AURKA rs2273535 T>A多态性与癌症总体风险增加有关,尤其是乳腺癌。需要进一步的验证实验来加强我们的结论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fca5/7357424/76cb00db5e17/fonc-10-01040-g0001.jpg

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