PRNCR1、PAX8AS1、MEG3和PTENP1基因多态性与乳腺癌风险的关系

Personalized medicine Pub Date : 2024-01-01 Epub Date: 2024-12-05 DOI:10.1080/17410541.2024.2435800
Anoosha Asadi, Fatemeh Barati, Alireza Nakhaee, Danial Jahantigh, Seyed-Mehdi Hashemi, Mohsen Taheri, Gholamreza Bahari
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引用次数: 0

摘要

目的:在本研究中,我们检测了BC患者PRNCR1 (rs13252298, rs1456315), PAX8-AS1 (rs4848320), MEG3 (rs7158663), PTENP1 (rs7853346)基因的多态性,并将其与伊朗人群中的健康个体进行了比较。方法:采用PCR- RFLP和PCR- tetra ARMS方法进行遗传多态性评价。结果与结论:结果显示rs13252298多态性的共显性、显性和G等位基因以及rs1456315多态性的显性与BC发病风险增加相关。rs4848320多态性的CT和TT基因型以及显性和T等位基因也是研究人群的危险因素。rs7158663多态性的AA基因型、显性、隐性和A等位基因以及rs7853346多态性的CC基因型增加了BC的发病风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association between PRNCR1, PAX8AS1, MEG3, and PTENP1 gene polymorphisms and breast cancer risk.

Aim: In this study, we examined the polymorphisms of PRNCR1 (rs13252298, rs1456315), PAX8-AS1 (rs4848320) MEG3 (rs7158663), PTENP1 (rs7853346) genes in BC patients and compared it with healthy individuals in an Iranian population.

Method: The assessment of genetic polymorphisms was conducted using PCR - RFLP and PCR-Tetra ARMS methods.

Results & conclusion: The results showed that Codominant, Dominant and G allele of rs13252298 polymorphism and Dominant of rs1456315 polymorphism are correlated with increased risk of BC. The CT and TT genotype and Dominant and T allele of rs4848320 polymorphism is also a risk factor in the study population. The genotype AA, dominant, recessive and A allele of rs7158663 polymorphism and also CC genotype of rs7853346 polymorphism increase the risk of BC.

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