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本文引用的文献

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Flap endonuclease 1 polymorphisms (rs174538 and rs4246215) contribute to an increased cancer risk: Evidence from a meta-analysis.瓣内切核酸酶1基因多态性(rs174538和rs4246215)与癌症风险增加有关:一项荟萃分析的证据。
Mol Clin Oncol. 2015 Nov;3(6):1347-1352. doi: 10.3892/mco.2015.617. Epub 2015 Jul 30.
2
Association of functional FEN1 genetic variants and haplotypes and breast cancer risk.功能 FEN1 基因变异和单倍型与乳腺癌风险的关联。
Gene. 2014 Mar 15;538(1):42-5. doi: 10.1016/j.gene.2014.01.025. Epub 2014 Jan 16.
3
Functional FEN1 genetic variants and haplotypes are associated with glioma risk.功能性 FEN1 基因变异和单倍型与胶质瘤风险相关。
J Neurooncol. 2013 Jan;111(2):145-51. doi: 10.1007/s11060-012-1007-0. Epub 2012 Nov 27.
4
Replication study of PLCE1 and C20orf54 polymorphism and risk of esophageal cancer in a Chinese population.PLCE1 和 C20orf54 多态性与中国人群食管癌风险的复制研究。
Mol Biol Rep. 2012 Sep;39(9):9105-11. doi: 10.1007/s11033-012-1782-x. Epub 2012 Jun 29.
5
Functional FEN1 genetic variants contribute to risk of hepatocellular carcinoma, esophageal cancer, gastric cancer and colorectal cancer.功能性 FEN1 遗传变异可增加肝癌、食管癌、胃癌和结直肠癌的发病风险。
Carcinogenesis. 2012 Jan;33(1):119-23. doi: 10.1093/carcin/bgr250. Epub 2011 Nov 9.
6
Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3.全基因组关联研究确定了染色体 2p16.3、2p21 和 9q33.3 上多囊卵巢综合征的易感性位点。
Nat Genet. 2011 Jan;43(1):55-9. doi: 10.1038/ng.732. Epub 2010 Dec 12.
7
MicroRNAs and esophageal squamous cell carcinoma.微小 RNA 与食管鳞状细胞癌。
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9
Functional FEN1 polymorphisms are associated with DNA damage levels and lung cancer risk.功能性FEN1基因多态性与DNA损伤水平及肺癌风险相关。
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10
Overexpression and hypomethylation of flap endonuclease 1 gene in breast and other cancers.乳腺癌及其他癌症中FEN1基因的过表达与低甲基化
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Flap endonuclease-1 rs174538 G>A 多态性与中国人群食管癌风险相关。

Flap endonuclease-1 rs174538 G>A polymorphisms are associated with the risk of esophageal cancer in a Chinese population.

机构信息

Department of Cardiothoracic Surgery, The Second Affiliated Hospital of Soochow University, Suzhou, China.

Department of Rheumatology, The Second Affiliated Hospital of Soochow University, Suzhou, China.

出版信息

Thorac Cancer. 2017 May;8(3):192-196. doi: 10.1111/1759-7714.12422. Epub 2017 Mar 20.

DOI:10.1111/1759-7714.12422
PMID:28319330
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5415465/
Abstract

BACKGROUND

Esophageal cancer has a high mortality rate, particularly in Asia, and there are obvious racial differences in regard to incidence. The purpose of our study was to assess the genetic susceptibility of functional single nucleotide polymorphisms in flap endonuclease-1 (FEN1) in esophageal squamous cell carcinoma ESCC.

METHODS

Clinical blood samples of 629 ESCC cases and 686 control samples were collected. The ligation detection reaction method was used to determine FEN 1 rs174538 G>A genotypes.

RESULTS

A significantly decreased risk of ESCC was associated with FEN1 rs174538 GA genotypes among patients under 63 years old.

CONCLUSIONS

Our results suggest that functional polymorphism FEN1 rs174538 G>A might affect personal susceptibility to ESCC. This result provides a solid theoretical foundation for further clinical study using larger sample sizes.

摘要

背景

食管癌死亡率高,尤其在亚洲,且发病率存在明显的种族差异。本研究旨在评估 FEN1(flap endonuclease-1)基因中功能性单核苷酸多态性与食管鳞癌(ESCC)易感性的关系。

方法

收集 629 例 ESCC 病例和 686 例对照的临床血样。采用连接酶检测反应法检测 FEN1 rs174538 G>A 基因型。

结果

63 岁以下患者中,FEN1 rs174538 GA 基因型与 ESCC 风险显著降低相关。

结论

本研究结果提示,FEN1 rs174538 G>A 功能性多态性可能影响 ESCC 的个体易感性。该结果为进一步使用更大样本量进行临床研究提供了坚实的理论基础。