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XPG基因rs2094258多态性与胃癌风险的关联。

Association between the XPG gene rs2094258 polymorphism and risk of gastric cancer.

作者信息

Zhang Zhe, Yin Jiefeng, Xu Qi, Shi Jianfeng

机构信息

General Surgery Department, Tongde Hospital of Zhejiang Province, Hangzhou, China.

Department of Abdominal Medical Oncology, Zhejiang Cancer Hospital, Hangzhou, China.

出版信息

J Clin Lab Anal. 2018 Oct;32(8):e22564. doi: 10.1002/jcla.22564. Epub 2018 May 7.

DOI:10.1002/jcla.22564
PMID:29732643
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6816837/
Abstract

BACKGROUND

Xeroderma pigmentosum group G (XPG) plays an important role in maintaining the stability and integrity of genomic DNA. Previous studies demonstrate some XPG gene polymorphisms are associated with susceptibility to gastric cancer (GC).

METHODS

The association between XPG rs2094258 polymorphism and GC risk was investigated first by a hospital-based case-control study involving 386 patients and 439 controls and then by a meta-analysis. The polymorphism was genotyped by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLR).

RESULTS

Xeroderma pigmentosum group G rs2094258 polymorphism was associated with an increased risk of GC in a Chinese population. The meta-analysis did not reveal any significant difference in the overall population. Subgroup analysis of geographic locations showed a significant association between the XPG gene rs2094258 polymorphism and GC risk in Southern China. Stratification analysis further indicated significant associations in hospital-based studies and studies using PCR-RFLR.

CONCLUSION

Xeroderma pigmentosum group G gene rs2094258 polymorphism may be associated with an increased risk of GC in Southern China. Nevertheless, the findings of this meta-analysis should be validated by well-designed large-scale case-control studies among other ethnicities.

摘要

背景

着色性干皮病G组(XPG)在维持基因组DNA的稳定性和完整性方面发挥着重要作用。先前的研究表明,一些XPG基因多态性与胃癌(GC)易感性相关。

方法

首先通过一项基于医院的病例对照研究(涉及386例患者和439例对照),然后通过荟萃分析,研究XPG rs2094258多态性与GC风险之间的关联。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLR)对该多态性进行基因分型。

结果

在中国人群中,着色性干皮病G组rs2094258多态性与GC风险增加相关。荟萃分析未显示总体人群中有任何显著差异。地理位置亚组分析显示,XPG基因rs2094258多态性与中国南方的GC风险之间存在显著关联。分层分析进一步表明,在基于医院的研究和使用PCR-RFLR的研究中存在显著关联。

结论

着色性干皮病G组基因rs2094258多态性可能与中国南方GC风险增加相关。然而,这一荟萃分析的结果应通过在其他种族中精心设计的大规模病例对照研究进行验证。

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本文引用的文献

1
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Aging (Albany NY). 2016 Dec 6;8(12):3311-3320. doi: 10.18632/aging.101119.
2
Investigation on ERCC5 genetic polymorphisms and the development of gastric cancer in a Chinese population.中国人群中ERCC5基因多态性与胃癌发生的研究
Genet Mol Res. 2016 Aug 26;15(3):gmr8364. doi: 10.4238/gmr.15038364.
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Identification of biomarkers for pseudo and true progression of GBM based on radiogenomics study.基于放射基因组学研究鉴定胶质母细胞瘤假性和真性进展的生物标志物
Oncotarget. 2016 Aug 23;7(34):55377-55394. doi: 10.18632/oncotarget.10553.
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Polymorphisms of multiple genes involved in NER pathway predict prognosis of gastric cancer.参与核苷酸切除修复(NER)途径的多个基因的多态性可预测胃癌的预后。
Oncotarget. 2016 Jul 26;7(30):48130-48142. doi: 10.18632/oncotarget.10173.
5
Association between XPG gene polymorphisms and development of gastric cancer risk in a Chinese population.中国人群中XPG基因多态性与胃癌发生风险的关联
Genet Mol Res. 2016 Jun 10;15(2):gmr7877. doi: 10.4238/gmr.15027877.
6
Lack of association between ERCC5 gene polymorphisms and gastric cancer risk in a Chinese population.中国人群中ERCC5基因多态性与胃癌风险之间无关联。
Genet Mol Res. 2016 Jun 10;15(2):gmr7779. doi: 10.4238/gmr.15027779.
7
Association between the XPG gene Asp1104His polymorphism and lung cancer risk.XPG基因Asp1104His多态性与肺癌风险之间的关联。
Genet Mol Res. 2016 Jun 10;15(2):gmr7395. doi: 10.4238/gmr.15027395.
8
Association of potentially functional variants in the XPG gene with neuroblastoma risk in a Chinese population.中国人群中XPG基因潜在功能变异与神经母细胞瘤风险的关联。
J Cell Mol Med. 2016 Aug;20(8):1481-90. doi: 10.1111/jcmm.12836. Epub 2016 Mar 28.
9
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Oncotarget. 2016 Mar 8;7(10):11724-32. doi: 10.18632/oncotarget.7352.
10
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J Cell Mol Med. 2016 May;20(5):903-8. doi: 10.1111/jcmm.12773. Epub 2016 Jan 28.