Department of Medical Biological Disciplines, Belgorod State National Research University, 308015 Belgorod, Russia.
Int J Mol Sci. 2022 Oct 20;23(20):12638. doi: 10.3390/ijms232012638.
We conducted this study to explore the association between matrix metalloproteinase (MMP) gene polymorphisms and breast cancer (BC) risk in the Caucasian women of Russia. In total, 358 affected (BC) and 746 unaffected (cancer-free) women were included in this case-control retrospective study. From BC-related genes in previous studies, ten single nucleotide polymorphisms (SNPs) in five MMP genes (MMP1, 2, 3, 8, 9) were genotyped. The BC risk was calculated by logistic regression (to evaluate the SNPs’ independent effects) and model-based multifactor dimensionality reduction (MB-MDR) (to identify SNP−SNP interactions) methods. The allelic variants’ distribution of c.836 A > G (rs17576) and c. 1721 C > G (rs2250889) MMP9 was significantly different between BC and cancer-free women: for G minor alleles, these SNPs manifested disorder protective effects (OR 0.82 and OR 0.67−0.71, respectively, pperm ≤ 0.035). Eleven haplotypes of six SNPs MMP9 were involved in BC risk (nine haplotypes) and protective (two haplotypes) effects. All 10 SNPs of the MMP genes examined were associated with BC within the 13 SNP−SNP interaction simulated models, with a pivotal role of the two-locus (rs17577 × rs3918242) MMP9 epistatic interaction (defined as 1.81% BC entropy within more than 60% of the genetic models). Under in silico bioinformatics, BC susceptibility MMP polymorphic loci are located in functionally active genome regions and impact genes expression and splicing “regulators” in the mammary gland. The biological pathways of BC MMP candidate genes are mainly realized due to metalloendopeptidase activity and extracellular matrix organization (structure, disassembly, metabolic process, etc.). In conclusion, our data show that MMP gene polymorphisms are related to BC susceptibility in the Caucasian women of Russia.
我们进行了这项研究,以探讨基质金属蛋白酶(MMP)基因多态性与俄罗斯白种女性乳腺癌(BC)风险之间的关联。在这项病例对照回顾性研究中,共纳入 358 名患病(BC)和 746 名未患病(无癌症)女性。从先前的 BC 相关基因研究中,我们对五个 MMP 基因(MMP1、2、3、8、9)中的 10 个单核苷酸多态性(SNP)进行了基因分型。通过逻辑回归(评估 SNP 的独立影响)和基于模型的多维降维(MB-MDR)(识别 SNP-SNP 相互作用)方法计算 BC 风险。C.836 A > G(rs17576)和 C.1721 C > G(rs2250889)MMP9 的等位变体分布在 BC 和无癌女性之间存在显著差异:对于 G 等位变体,这些 SNP 表现出紊乱保护作用(OR 0.82 和 OR 0.67-0.71,分别,pperm ≤ 0.035)。MMP9 的六个 SNP 的 11 个单倍型涉及 BC 风险(9 个单倍型)和保护(2 个单倍型)作用。在所检查的 MMP 基因的 10 个 SNP 中,有 10 个 SNP 在 13 个 SNP-SNP 相互作用模拟模型中与 BC 相关,其中两个位点(rs17577×rs3918242)MMP9 上位性相互作用起着关键作用(在 60%以上的遗传模型中定义为 1.81%的 BC 熵)。在计算机生物信息学中,BC 易感性 MMP 多态性位点位于功能活跃的基因组区域,并影响乳腺中的基因表达和剪接“调节剂”。BC MMP 候选基因的生物途径主要通过金属内肽酶活性和细胞外基质组织(结构、分解、代谢过程等)来实现。总之,我们的数据表明 MMP 基因多态性与俄罗斯白种女性的 BC 易感性有关。