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基因多态性 rs1801516(G > A)与总体癌症风险无关:一项更新的荟萃分析。

Polymorphism rs1801516 (G > A) in the gene is not associated with overall cancer risk: an updated meta-analysis.

机构信息

Department of Breast Surgery, Cancer Hospital of China Medical University, Shenyang, Liaoning Province, P.R. China.

Department of Bone Surgery, People's Hospital of Liaoning Province, Shenyang, Liaoning Province, P.R. China.

出版信息

J Int Med Res. 2020 Jul;48(7):300060520937618. doi: 10.1177/0300060520937618.

DOI:10.1177/0300060520937618
PMID:32674635
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7370572/
Abstract

OBJECTIVE

The ataxia telangiectasia mutated () gene contains a functional single nucleotide polymorphism (SNP) rs1801516 (G > A) that may be associated with cancer risk. This meta-analysis aimed to interrogate the relationship between rs1801516 and cancer occurrence and disease etiology.

METHODS

We retrieved and identified the available case-control studies that met the inclusion criteria from the PubMed, Web of Science, and Embase databases. Odds ratio (OR) and 95% confidence intervals (CIs) were used to measure the association between rs1801516 and cancer risk. Additionally, we performed sensitivity, subgroup, and publication bias analyses.

RESULTS

After inclusion criteria were met, the meta-analysis included 29 studies, with 9,453 cancer patients (cases) and 14,646 controls. No association was found between rs1801516 and cancer risk (pooled OR = 0.911; 95% CI, 0.740-1.123). Concordantly, no association was found between rs1801516 and cancer risk after subgroup analysis by source of controls, cancer type, or ethnicity, which confirmed the finding of the dominant model that this SNP is not involved in the occurrence of cancer.

CONCLUSIONS

Through this meta-analysis, we found no association between rs1801516 and cancer occurrence as a risk factor. These data provide useful information for future case-control studies on cancer etiology.

摘要

目的

共济失调毛细血管扩张突变()基因包含一个功能性的单核苷酸多态性(SNP)rs1801516(G>A),可能与癌症风险相关。本荟萃分析旨在探讨 rs1801516 与癌症发生和疾病病因的关系。

方法

我们从 PubMed、Web of Science 和 Embase 数据库中检索并确定了符合纳入标准的可用病例对照研究。比值比(OR)和 95%置信区间(CI)用于衡量 rs1801516 与癌症风险之间的关联。此外,我们还进行了敏感性、亚组和发表偏倚分析。

结果

符合纳入标准后,荟萃分析纳入了 29 项研究,共 9453 名癌症患者(病例)和 14646 名对照。rs1801516 与癌症风险之间没有关联(合并 OR=0.911;95%CI,0.740-1.123)。同样,在按对照来源、癌症类型或种族进行亚组分析后,也没有发现 rs1801516 与癌症风险之间的关联,这证实了该 SNP 不参与癌症发生的显性模型的发现。

结论

通过这项荟萃分析,我们没有发现 rs1801516 与癌症发生作为危险因素之间的关联。这些数据为未来癌症病因学的病例对照研究提供了有用的信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab53/7370572/5f69eb8d0cb6/10.1177_0300060520937618-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab53/7370572/4adbb10ed294/10.1177_0300060520937618-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab53/7370572/888f7c211134/10.1177_0300060520937618-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab53/7370572/4c1859b97bf0/10.1177_0300060520937618-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab53/7370572/5f69eb8d0cb6/10.1177_0300060520937618-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab53/7370572/4adbb10ed294/10.1177_0300060520937618-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab53/7370572/888f7c211134/10.1177_0300060520937618-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab53/7370572/4c1859b97bf0/10.1177_0300060520937618-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab53/7370572/5f69eb8d0cb6/10.1177_0300060520937618-fig4.jpg

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本文引用的文献

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J Cell Mol Med. 2018 Jul;22(7):3671-3678. doi: 10.1111/jcmm.13650. Epub 2018 Apr 24.
2
Targeted next generation sequencing identifies functionally deleterious germline mutations in novel genes in early-onset/familial prostate cancer.靶向下一代测序鉴定早发性/家族性前列腺癌中新基因中的功能丧失性种系突变。
PLoS Genet. 2018 Apr 16;14(4):e1007355. doi: 10.1371/journal.pgen.1007355. eCollection 2018 Apr.
3
Ataxia-Telangiectasia Mutated Kinase in the Control of Oxidative Stress, Mitochondria, and Autophagy in Cancer: A Maestro With a Large Orchestra.
共济失调毛细血管扩张症突变激酶在癌症中对氧化应激、线粒体和自噬的调控:一位指挥大型管弦乐队的大师。
Front Oncol. 2018 Mar 16;8:73. doi: 10.3389/fonc.2018.00073. eCollection 2018.
4
Genetic determinants of sporadic breast cancer in Sri Lankan women.斯里兰卡女性散发性乳腺癌的遗传决定因素。
BMC Cancer. 2018 Feb 13;18(1):180. doi: 10.1186/s12885-018-4112-4.
5
A meta-analysis of data associating gene polymorphisms with schizophrenia.一项关于基因多态性与精神分裂症相关性数据的荟萃分析。
Neuropsychiatr Dis Treat. 2018 Jan 3;14:153-164. doi: 10.2147/NDT.S156479. eCollection 2018.
6
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Aging (Albany NY). 2017 Feb 22;9(2):547-555. doi: 10.18632/aging.101177.
7
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