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维生素D受体基因中的FokI多态性与白人女性患乳腺癌的风险

FokI polymorphism in vitamin D receptor gene and risk of breast cancer among Caucasian women.

作者信息

Shan Jin-lu, Dai Nan, Yang Xue-qin, Qian Cheng-yuan, Yang Zhen-zhou, Jin Feng, Li Mengxia, Wang Dong

机构信息

Cancer Center, Research Institute of Surgery and Daping Hospital, Third Military Medical University, No.10 Changjiang Zhilu, Yuzhong District, Chongqing, 400042, China.

出版信息

Tumour Biol. 2014 Apr;35(4):3503-8. doi: 10.1007/s13277-013-1462-z. Epub 2013 Dec 8.

Abstract

Vitamin D plays a central role in cellular proliferation, apoptosis induction, and tumor growth suppression. The vitamin D receptor (VDR) is a crucial mediator for the cellular effects of vitamin D. A series of epidemiological studies have examined the association between the VDR FokI polymorphism and breast cancer risk, but the findings remain inconclusive. Fifteen eligible case-control studies involving 15,681 cancer cases and 20,632 control subjects were identified through searching PubMed, Embase, and Web of Science. Odds ratios (ORs) and 95% confidence intervals (CIs) were used to assess the association. Heterogeneity across studies was examined with the chi-square-based Q test and the I (2) index. Begg's and Egger's test were also performed to determine publication bias. All statistical data were analyzed by STATA software. The combined estimates did not show significant risks correlated with the FokI polymorphism. However, we found an increased risk in the subgroup analysis by source of control (OR = 1.11, 95% CI = 1.01-1.22; heterogeneity test: P = 0.116, I(2) = 0.0% for ff vs FF; OR = 1.10, 95% CI = 1.01-1.21; heterogeneity test: P = 0.832, I(2) = 0.0% for ff vs Ff + FF). This meta-analysis suggests that the presence of FokI polymorphism may contribute to the risk of breast cancer in Caucasians.

摘要

维生素D在细胞增殖、诱导细胞凋亡和抑制肿瘤生长中起着核心作用。维生素D受体(VDR)是维生素D细胞效应的关键介质。一系列流行病学研究探讨了VDR FokI基因多态性与乳腺癌风险之间的关联,但研究结果仍无定论。通过检索PubMed、Embase和Web of Science数据库,确定了15项符合条件的病例对照研究,共纳入15681例癌症病例和20632例对照。采用比值比(OR)和95%置信区间(CI)评估关联。通过基于卡方的Q检验和I²指数检验研究间的异质性。还进行了Begg检验和Egger检验以确定发表偏倚。所有统计数据均使用STATA软件进行分析。合并估计结果未显示FokI基因多态性与显著风险相关。然而,我们在按对照来源进行的亚组分析中发现风险增加(ff与FF相比:OR = 1.11,95% CI = 1.01 - 1.22;异质性检验:P = 0.116,I² = 0.0%;ff与Ff + FF相比:OR = 1.10,95% CI = 1.01 - 1.21;异质性检验:P = 0.832,I² = 0.0%)。这项荟萃分析表明,FokI基因多态性的存在可能增加白种人患乳腺癌的风险。

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