Department of Molecular Biology & Genetics, Krishna Vishwa Vidyapeeth (Deemed to be University), Taluka-Karad, Dist- Satara, Pin-415 539, (Maharashtra) India.
Department of Oncology, Krishna Vishwa Vidyapeeth (Deemed to be University), Taluka- Karad, Dist- Satara, Pin-415 539, (Maharashtra) India.
Asian Pac J Cancer Prev. 2023 Sep 1;24(9):3065-3075. doi: 10.31557/APJCP.2023.24.9.3065.
At present very little information is available on combined effects of DNA repair genes with tumor suppressor gene polymorphisms and their association with cancer susceptibility. No such association studies have been carried out with breast cancer or any other cancer from India. Present study was conducted to study the combined effects of SNPs of XRCC1, XRCC2, XRCC3 with Arg72Pro and Arg249Ser SNPs of TP53 gene in risk of BC in rural parts of India.
The polymorphisms of Arg194Trp, Arg280His, Arg399Gln of XRCC1, Arg188His of XRCC2 and Thr241Met of XRCC3 with Arg72Pro and Arg249Ser of TP53 gene polymorphisms was studied by polymerase chain reaction-based restriction fragment length polymorphism (PCR-RFLP) method. The association among the polymorphisms with breast cancer risk was studied by Odds ratio within 95% confidence interval and SNP-SNP interaction were confirmed by logistic regression analysis.
The results of genotype frequency distribution of XRCC1, XRCC2, XRCC3 genotypes showed positive association between XRCC1 Arg280His polymorphism and BC risk (OR=4.54; 95% CI: 3.36- 6.15; p<0.0001). Also the heterozygous genotypes Arg188His of XRCC2 (OR=1.58; 95% CI: 1.13- 2.21; p=0.007) and Thr241Met genotype of XRCC3 (OR=2.13; 95% CI: 1.44- 3.13; p=0.0001) were associated with BC risk. The combination of heterozygous Arg280His genotype of XRCC1 along with Arg72Pro genotype of TP53 increased the risk of BC (OR=4.53; 95% CI: 2.85-7.20); p<0.0001). Similarly, the combined effect of heterozygous Arg/His genotype of XRCC1 with heterozygous Arg/Ser genotype of TP53 at codon 249 showed significant association with increased BC risk (OR=5.08; 95% CI: 2.86-9.04); p<0.0001).
The findings derived from our study concluded that the heterozygous variant Arg280His genotype of XRCC1 and Thr241Met polymorphism of XRCC3 in combination with heterozygous arginine72proline genotype and heterozygous Arg249Ser polymorphism of TP53 showed significant association with breast cancer risk in Maharashtrian women.
目前,关于 DNA 修复基因与肿瘤抑制基因多态性的联合作用及其与癌症易感性的关系的信息非常有限。尚未对印度的乳腺癌或任何其他癌症进行过此类关联研究。本研究旨在探讨 XRCC1 的 Arg194Trp、Arg280His、Arg399Gln 位点的单核苷酸多态性(SNP)与 XRCC2 的 Arg188His 以及 XRCC3 的 Thr241Met 位点与 TP53 基因 Arg72Pro 和 Arg249Ser 多态性的联合效应对印度农村地区乳腺癌(BC)发病风险的影响。
采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法检测 XRCC1 的 Arg194Trp、Arg280His、Arg399Gln 多态性,XRCC2 的 Arg188His 和 XRCC3 的 Thr241Met 多态性与 TP53 基因 Arg72Pro 和 Arg249Ser 多态性的关系。通过 95%置信区间的优势比研究多态性与乳腺癌风险之间的关联,并通过逻辑回归分析证实 SNP-SNP 相互作用。
XRCC1、XRCC2、XRCC3 基因型的基因型频率分布结果显示,XRCC1 Arg280His 多态性与 BC 风险呈正相关(OR=4.54;95%CI:3.36-6.15;p<0.0001)。此外,XRCC2 的杂合型 Arg188His (OR=1.58;95%CI:1.13-2.21;p=0.007)和 XRCC3 的 Thr241Met 基因型(OR=2.13;95%CI:1.44-3.13;p=0.0001)与 BC 风险相关。XRCC1 杂合型 Arg280His 基因型与 TP53 Arg72Pro 基因型的组合增加了 BC 的发病风险(OR=4.53;95%CI:2.85-7.20;p<0.0001)。同样,XRCC1 杂合型 Arg/His 基因型与 TP53 密码子 249 处的杂合型 Arg/Ser 基因型的联合作用与 BC 风险增加显著相关(OR=5.08;95%CI:2.86-9.04;p<0.0001)。
本研究结果表明,XRCC1 的 Arg280His 杂合变体基因型和 XRCC3 的 Thr241Met 多态性与 TP53 的异亮氨酸 72 脯氨酸基因型和异亮氨酸 249 丝氨酸基因型的杂合变体联合与马哈拉施特拉邦妇女的乳腺癌风险显著相关。