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基因多态性与孟加拉国人群结直肠癌易感性的关联:病例对照分析。

Polymorphisms in Gene and Susceptibility of Colorectal Cancer in Bangladeshi Population: A Case-Control Analysis.

机构信息

Department of Pharmacy, 214341University of Asia Pacific, Dhaka, Bangladesh.

Department of Pharmacy, State University of Bangladesh, Dhaka, Bangladesh.

出版信息

Cancer Control. 2022 Jan-Dec;29:10732748221143879. doi: 10.1177/10732748221143879.

DOI:10.1177/10732748221143879
PMID:36458977
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9720807/
Abstract

OBJECTIVE

Interleukin-17A () genetic polymorphisms are associated with multiple cancer types, including colorectal cancer (CRC). However, no previous study was performed in the Bangladeshi population to evaluate the association. Our study aimed to find the association between two variants (rs10484879 C/A and rs3748067 G/A) and susceptibility of CRC.

METHODS AND MATERIALS

This retrospective case-control study comprised 292 CRC patients and 288 age, sex, and BMI matched healthy volunteers. Genotyping of both variants was done by the tetra-primer ARMS-PCR method, and the results were analyzed by the SPSS software package (version-25.0).

RESULTS

Logistic regression analysis indicated that in case of rs10484879 polymorphism, AC and AA genotype carriers showed 2.44- and 3.27-times significantly increased risk for CRC development (OR = 2.44, P = .0008 and OR = 3.27, P = .0133, individually). A significant association was also observed for AC + AA genotype (OR = 2.58, P = .0001). Again, over-dominant and allelic model revealed statistically significant link to CRC risk (OR = 2.13, P = .0035 and OR = 2.22, P = .001). For rs3748067 polymorphism, AG and AA genotype carriers showed 2.30- and 2.45-times enhanced risk for CRC (OR = 2.30, P = .005 and OR = 2.45, P = .031). A statistically significant association was also observed for AG + AA genotype (OR = 2.35, P = .001), over-dominant model (OR = 2.05, P = .014), and allelic model (OR = 2.11, P = .0004).

CONCLUSION

This study highlights that rs10484879 and rs3748067 polymorphisms may be associated with CRC development. However, further functional research with larger samples may reveal more statistically significant outcomes.

摘要

目的

白细胞介素-17A() 基因多态性与多种癌症类型相关,包括结直肠癌(CRC)。然而,以前没有在孟加拉国人群中进行过评估这种关联的研究。我们的研究旨在寻找两个变体(rs10484879C/A 和 rs3748067G/A)与 CRC 易感性之间的关联。

方法和材料

这项回顾性病例对照研究包括 292 名 CRC 患者和 288 名年龄、性别和 BMI 匹配的健康志愿者。通过四引物 ARMS-PCR 方法对这两种变体进行基因分型,并使用 SPSS 软件包(版本 25.0)进行分析。

结果

逻辑回归分析表明,在 rs10484879 多态性的情况下,AC 和 AA 基因型携带者患 CRC 的风险分别增加了 2.44 倍和 3.27 倍(OR=2.44,P=0.0008 和 OR=3.27,P=0.0133,单独)。AC+AA 基因型也存在显著相关性(OR=2.58,P=0.0001)。同样,过显性和等位基因模型也显示与 CRC 风险有统计学意义的联系(OR=2.13,P=0.0035 和 OR=2.22,P=0.001)。对于 rs3748067 多态性,AG 和 AA 基因型携带者患 CRC 的风险分别增加了 2.30 倍和 2.45 倍(OR=2.30,P=0.005 和 OR=2.45,P=0.031)。AG+AA 基因型也存在显著相关性(OR=2.35,P=0.001),过显性模型(OR=2.05,P=0.014)和等位基因模型(OR=2.11,P=0.0004)。

结论

本研究表明,rs10484879 和 rs3748067 多态性可能与 CRC 的发生有关。然而,进一步的功能研究需要更大的样本量,可能会揭示出更具统计学意义的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f926/9720807/9333b993aec4/10.1177_10732748221143879-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f926/9720807/c3d3a5cc6f10/10.1177_10732748221143879-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f926/9720807/9333b993aec4/10.1177_10732748221143879-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f926/9720807/c3d3a5cc6f10/10.1177_10732748221143879-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f926/9720807/9333b993aec4/10.1177_10732748221143879-fig2.jpg

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