Almeida Micaela, Soares Mafalda, Fonseca-Moutinho José, Ramalhinho Ana Cristina, Breitenfeld Luiza
Health Sciences Research Centre (CICS), Faculty of Health Sciences, University of Beira Interior (UBI), Avenida Infante D. Henrique, 6200-506 Covilhã, Portugal.
Academic Hospital of Cova da Beira (CHUCB), Quinta do Alvito, 6200-251 Covilhã, Portugal.
Pharmaceuticals (Basel). 2021 Jan 27;14(2):94. doi: 10.3390/ph14020094.
Estrogen metabolism plays an important role in tumor initiation and development. Lifetime exposure to high estrogens levels and deregulation of enzymes involved in estrogen biosynthetic and metabolic pathway are considered risk factors for breast cancer. The present study aimed to evaluate the impact of mutations acquisition during the lifetime in low penetrance genes that codify enzymes responsible for estrogen detoxification. Genotype analysis of and null polymorphisms, Val432Leu and C677T polymorphisms was performed in 157 samples of women with hormone-dependent breast cancer and correlated with the age at diagnosis. The majority of patients with null genotype and with both and null genotypes were 50 years old or more at the diagnosis (-value = 0.021 and 0.018, respectively). Older women with null genotype were also carriers of the Val allele (-value = 0.012). As well, null and Val genotypes were correlated with diagnosis at later ages (-value = 0.022). Similar results were found associating C677T and null polymorphism (-value = 0.034). Our results suggest that estrogen metabolic pathway polymorphisms constitute a factor to be considered simultaneously with models for breast cancer risk assessment.
雌激素代谢在肿瘤的发生和发展中起着重要作用。终生暴露于高水平雌激素以及雌激素生物合成和代谢途径中相关酶的失调被认为是乳腺癌的危险因素。本研究旨在评估终生获得的低外显率基因突变对编码负责雌激素解毒酶的影响。对157例激素依赖性乳腺癌女性患者的样本进行了 和 无效多态性、 Val432Leu和 C677T多态性的基因型分析,并与诊断年龄相关联。大多数 无效基因型以及 和 均为无效基因型的患者在诊断时年龄为50岁或以上( 值分别为0.021和0.018)。具有 无效基因型的老年女性也是Val等位基因的携带者( 值 = 0.012)。同样, 无效和Val基因型与较晚年龄的诊断相关( 值 = 0.022)。在将 C677T和 无效多态性相关联时也发现了类似结果( 值 = 0.034)。我们的结果表明,雌激素代谢途径多态性是乳腺癌风险评估模型中需要同时考虑的一个因素。