Habel Azza F, Ghali Rabeb M, Bouaziz Hanen, Daldoul Amira, Hadj-Ahmed Mariem, Mokrani Amina, Zaied Sonia, Hechiche Monia, Rahal Khaled, Yacoubi-Loueslati Besma, Almawi Wassim Y
1 Laboratory of Mycology, Pathologies and Biomarkers (LR16ES05), Faculty of Sciences of Tunis, University Tunis El Manar, Tunis, Tunisia.
2 Faculty of Pharmacy of Monastir, University of Monastir, Monastir, Tunisia.
Tumour Biol. 2019 Apr;41(4):1010428319845749. doi: 10.1177/1010428319845749.
A role for matrix metalloproteinase polymorphisms in breast cancer development and progression was proposed, but with inconclusive results. We assessed the relation of matrix metalloproteinase-2 variants with breast cancer and related phenotypes in Tunisians. This case-control retrospective study involved 430 women with breast cancer and 498 healthy controls. Genotyping of matrix metalloproteinase-2 rs243866, rs243865, rs243864, and rs2285053 was analyzed by allelic exclusion. The minor allele frequency of rs2285053 was significantly lower in women with breast cancer cases as compared to control women; minor allele frequencies of the remaining single-nucleotide polymorphisms were similar between cases and control women. The distribution of rs243865 and rs2285053 genotypes was significantly different between breast cancer patients and control subjects. This persisted when key covariates were controlled for. None of the matrix metalloproteinase-2 variants were associated with estrogen receptor positivity, progesterone receptor positivity, or with double estrogen receptor-progesterone receptor positivity in breast cancer patients. Matrix metalloproteinase-2 rs243866, rs243865, and rs243864 were positively associated with menstrual irregularity and histological type, while rs243866 and rs2285053 were negatively associated with menarche and nodal status. In addition, rs2285053 was negatively associated with triple negativity, tumor size, distance metastasis, molecular type, and chemotherapy. Haploview analysis revealed high linkage disequilibrium between matrix metalloproteinase-2 variants. Four-locus Haploview analysis identified haplotypes GCTT and GTTC to be negatively associated with breast cancer, which remained statistically after controlling for key covariates. Matrix metalloproteinase-2 alleles and genotypes, along with four-locus haplotypes, are related to reduced susceptibility to breast cancer in Tunisian women, suggesting a protective effect.
有人提出基质金属蛋白酶多态性在乳腺癌发生和发展中起作用,但结果尚无定论。我们评估了突尼斯人基质金属蛋白酶-2变体与乳腺癌及相关表型之间的关系。这项病例对照回顾性研究纳入了430例乳腺癌女性患者和498例健康对照者。通过等位基因排除法分析了基质金属蛋白酶-2 rs243866、rs243865、rs243864和rs2285053的基因分型。与对照女性相比,乳腺癌患者中rs2285053的次要等位基因频率显著降低;其余单核苷酸多态性的次要等位基因频率在病例组和对照组女性之间相似。rs243865和rs2285053基因型的分布在乳腺癌患者和对照受试者之间存在显著差异。在控制关键协变量后,这种差异仍然存在。在乳腺癌患者中,没有一种基质金属蛋白酶-2变体与雌激素受体阳性、孕激素受体阳性或雌激素受体-孕激素受体双阳性相关。基质金属蛋白酶-2 rs243866、rs243865和rs243864与月经不规律和组织学类型呈正相关,而rs243866和rs2285053与初潮和淋巴结状态呈负相关。此外,rs2285053与三阴性、肿瘤大小、远处转移、分子类型和化疗呈负相关。Haploview分析显示基质金属蛋白酶-2变体之间存在高度连锁不平衡。四位点Haploview分析确定单倍型GCTT和GTTC与乳腺癌呈负相关,在控制关键协变量后,这种相关性在统计学上仍然存在。基质金属蛋白酶-2等位基因和基因型,以及四位点单倍型,与突尼斯女性乳腺癌易感性降低有关,提示具有保护作用。