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HFE基因中H63D多态性与实体癌发病率增加的关联:一项荟萃分析。

Implicating the H63D polymorphism in the HFE gene in increased incidence of solid cancers: a meta-analysis.

作者信息

Shen L L, Gu D Y, Zhao T T, Tang C J, Xu Y, Chen J F

机构信息

Department of Oncology, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.

Department of Oncology, Nanjing First Hospital, Nanjing Medical University, Nanjing, China

出版信息

Genet Mol Res. 2015 Oct 29;14(4):13735-45. doi: 10.4238/2015.October.28.36.

Abstract

A number of previous studies have demonstrated that the HFE H63D polymorphism is associated with increased risk of incidence multiple types of cancer, including colorectal cancer, breast cancer, liver cancer, pancreatic cancer, and gynecological malignant tumors. However, the clinical outcomes were inconsistent. Therefore, this meta-analysis was conducted to summarize the effect of the H63D variant on the incidence of solid tumor. PubMed and EMBASE databases were searched for articles associating the HFE H63D polymorphism with cancer risk. The relationships were evaluated by calculating the pooled odds ratios (ORs) with 95% confidence intervals (CIs). A total of 28 studies, including 7728 cancer cases and 11,895 controls, were identified. Statistically significant associations were identified between the HFE H63D polymorphism and solid cancer risk (CG vs CC, OR = 1.14, 95%CI = 1.07-1.23, P < 0.001; GG vs CC, OR = 1.28, 95%CI = 1.06-1.55, P = 0.010; CG/GG vs CC, OR = 1.16, 95%CI = 1.08-1.24, P < 0.001; GG vs CC/CG, OR = 1.24, 95%CI = 1.02-1.49, P = 0.027). In the subgroup analysis, we illustrated the effect of the H63D polymorphism on hepatocellular carcinoma and pancreatic cancer risk, particularly in the Asian and African subgroups; however, this was not observed in gynecological malignant tumors. In summary, this analysis provided strong evidence that the HFE H63D polymorphism may play a critical role in the increased aggressiveness of hepatocellular carcinoma and pancreatic cancer.

摘要

此前的多项研究表明,HFE基因H63D多态性与多种癌症的发病风险增加有关,包括结直肠癌、乳腺癌、肝癌、胰腺癌和妇科恶性肿瘤。然而,临床结果并不一致。因此,进行了这项荟萃分析,以总结H63D变异对实体瘤发病率的影响。通过检索PubMed和EMBASE数据库,查找将HFE基因H63D多态性与癌症风险相关联的文章。通过计算合并比值比(OR)及95%置信区间(CI)来评估两者之间的关系。共纳入28项研究,包括7728例癌症病例和11895例对照。结果发现,HFE基因H63D多态性与实体癌风险之间存在统计学显著关联(CG与CC相比,OR = 1.14,95%CI = 1.(07 - 1.23),P < 0.001;GG与CC相比,OR = 1.28,95%CI = 1.06 - 1.55,P = 0.010;CG/GG与CC相比,OR = 1.16,95%CI = 1.08 - 1.24,P < 0.001;GG与CC/CG相比,OR = 1.24,95%CI = 1.02 - 1.49,P = 0.027)。在亚组分析中,我们阐述了H63D多态性对肝细胞癌和胰腺癌风险的影响,尤其是在亚洲和非洲亚组中;然而,在妇科恶性肿瘤中未观察到这种情况。总之,该分析提供了有力证据,表明HFE基因H63D多态性可能在肝细胞癌和胰腺癌侵袭性增加中起关键作用。

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