Department of Gynecology and Obstetrics, Key Laboratory of Obstetric and Gynecologic and Pediatric Diseases and Birth Defects of Ministry of Education, West China Second University Hospital, Sichuan University, Chengdu 610041, P.R. China.
Department of Gynecology and Obstetrics, Chengdu First People's Hospital, Chengdu 610041, P.R. China.
Biosci Rep. 2019 Mar 19;39(3). doi: 10.1042/BSR20181809. Print 2019 Mar 29.
The role of forkhead box P3 (FOXP3) protein in tumorigenesis has long been controversial and existing data on the association between gene polymorphisms and cancer susceptibility were inconsistent. Here, we conducted a meta-analysis to better clarify the relationship. A comprehensive search of studies published from July 2008 to June 2018 was conducted. The statistical analyses of the pooled odds ratios (ORs) and the corresponding 95% confidence intervals (95% CIs) were performed using the Revman 5.2 software. A total of 12 articles with 19 case-control studies and 10389 participants were included. Three polymorphisms and six cancer types were evaluated. While no significant results were observed in overall and breast cancer groups for rs3761548 (A/C) polymorphisms, the pooled data showed an elevated risk of cancer in variant AA genotypes and A allele for Chinese population (AA vs. AC+CC: OR = 1.61, 95% CI = 1.09, 2.39; AA vs. CC: OR = 1.74, 95% CI = 1.05, 2.89; A vs. C: OR = 1.34, 95% CI = 1.00, 1.78). Neither the overall group analyses nor the subgroup analyses stratified by cancer type and ethnicity proposed any significant association of rs2280883 (C/T) and rs3761549 (T/C) polymorphisms with cancer susceptibility. This meta-analysis suggested that rs3761548 (A/C) polymorphisms were associated with increased cancer risk in Chinese population while rs2280883 (C/T) and rs3761549 (T/C) polymorphisms were not. More large-sample researches with diverse ethnicities and cancer types are needed to draw a concrete conclusion.
叉头框蛋白 P3(FOXP3)蛋白在肿瘤发生中的作用一直存在争议,现有关于基因多态性与癌症易感性之间关系的数据也不一致。在这里,我们进行了一项荟萃分析,以更好地阐明这种关系。从 2008 年 7 月到 2018 年 6 月,我们对已发表的研究进行了全面检索。使用 Revman 5.2 软件对合并的优势比(OR)和相应的 95%置信区间(95%CI)进行了统计分析。共纳入 12 篇文章,包含 19 项病例对照研究和 10389 名参与者。评估了三种多态性和六种癌症类型。虽然 rs3761548(A/C)多态性在总体和乳腺癌组中没有观察到显著结果,但合并数据显示,在中国人群中,变异 AA 基因型和 A 等位基因增加了癌症风险(AA 与 AC+CC:OR=1.61,95%CI=1.09,2.39;AA 与 CC:OR=1.74,95%CI=1.05,2.89;A 与 C:OR=1.34,95%CI=1.00,1.78)。无论是总体组分析还是按癌症类型和种族分层的亚组分析,均未提出 rs2280883(C/T)和 rs3761549(T/C)多态性与癌症易感性之间存在显著关联。这项荟萃分析表明,rs3761548(A/C)多态性与中国人群癌症风险增加相关,而 rs2280883(C/T)和 rs3761549(T/C)多态性则不然。需要更多具有不同种族和癌症类型的大样本研究来得出具体结论。