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miR-3131 3- bp 插入/缺失多态性与乳腺癌患者易感性及临床病理特征的关系。

The Relationship between Pre-miR-3131 3-bp Insertion/Deletion Polymorphism and Susceptibility and Clinicopathological Characteristics of Patients with Breast Cancer.

机构信息

Department of Clinical Biochemistry, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran.

Children and Adolescent Health Research Center, Zahedan University of Medical Sciences, Zahedan, Iran.

出版信息

Microrna. 2020;9(3):216-223. doi: 10.2174/2211536608666190906111830.

Abstract

AIMS

This study aimed at examining the effect of 3-bp pre-miR-3131 insertion/deletion (ins/del) polymorphism on Breast Cancer (BC) risk.

OBJECTIVES

Totally 403 women including 199 BC patients and 204 women who have no cancer were included in this case-control study. Genotyping of miR-3131 3-bp ins/del polymorphism was performed by mismatch PCR-RFLP method.

METHODS

The findings expressed that the pre-miR-3131 3-bp ins/del variant was not related to the risk of BC in all genetic tested models. While, the ins/del genotype was related to late onset BC (OR=2.53, 95%CI=1.27-4.84, p=0.008).

RESULTS

Pooled results from the meta-analysis indicated to that the pre-miR-3131 ins/del is related to with an increased risk of cancer in heterozygous (OR=1.26, 95%CI=1.06-1.51, p=0.01), dominant (OR=1.33, 95%CI=1.14-1.54, p=0.0002), and allele (OR=1.24, 95%CI=1.06-1.45, p=0.006) genetics models.

CONCLUSION

It is concluded that, our findings did not support a relationship between pre-miR-3131 ins/del polymorphism and the risk of BC. While, this variant was significantly related to late onset BC. Combined results of this study with previous studies indicated that this polymorphism increased the risk of cancer. More studies in a study with larger population with variety of ethnicities are required to verify our findings.

摘要

目的

本研究旨在探讨微小 RNA-3131(miR-3131)前体 3 个碱基插入/缺失(ins/del)多态性对乳腺癌(BC)风险的影响。

目的

在这项病例对照研究中,共纳入了 403 名女性,包括 199 名 BC 患者和 204 名无癌症的女性。采用错配 PCR-RFLP 方法对 miR-3131 3 个碱基 ins/del 多态性进行基因分型。

方法

研究结果表明,miR-3131 前体 3 个碱基 ins/del 变异与所有遗传测试模型中的 BC 风险无关。然而,ins/del 基因型与发病较晚的 BC 相关(OR=2.53,95%CI=1.27-4.84,p=0.008)。

结果

荟萃分析的汇总结果表明,miR-3131 ins/del 与杂合子(OR=1.26,95%CI=1.06-1.51,p=0.01)、显性(OR=1.33,95%CI=1.14-1.54,p=0.0002)和等位基因(OR=1.24,95%CI=1.06-1.45,p=0.006)遗传模型中癌症风险增加相关。

结论

我们的研究结果不支持 miR-3131 ins/del 多态性与 BC 风险之间存在关系。然而,这种变体与发病较晚的 BC 显著相关。将本研究与之前的研究结果相结合表明,这种多态性增加了癌症的风险。需要在具有不同种族的更大人群中进行更多的研究来验证我们的发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f54/7366006/cf9c8cbf0728/MIRNA-9-216_F1.jpg

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