Król Magdalena B, Galicki Michał, Grešner Peter, Wieczorek Edyta, Jabłońska Ewa, Reszka Edyta, Morawiec Zbigniew, Wąsowicz Wojciech, Gromadzińska Jolanta
Department of Biological and Environmental Monitoring, Nofer Institute of Occupational Medicine, Łódź, Poland.
Department of Surgical Oncology, Copernicus Memorial Hospital, Cancer Center, Łódź, Poland.
Acta Biochim Pol. 2018;65(1):51-57. doi: 10.18388/abp.2016_1425. Epub 2018 Mar 15.
The aim of this study was to establish whether the gene expression of estrogen receptor alpha (encoded by ESR1) correlates with the expression of glutathione peroxidase 1 (encoded by GPX1) in the tumor and adjacent tumor-free breast tissue, and whether this correlation is affected by breast cancer. Such relationships may give further insights into breast cancer pathology with respect to the status of estrogen receptor.
We used the quantitative real-time PCR technique to analyze differences in the expression levels of the ESR1 and GPX1 genes in paired malignant and non-malignant tissues from breast cancer patients.
ESR1 and GPX1 expression levels were found to be significantly down-regulated by 14.7% and 7.4% (respectively) in the tumorous breast tissue when compared to the non-malignant one. Down-regulation of these genes was independent of the tumor histopathology classification and clinicopathological factors, while the ESR1 mRNA level was reduced with increasing tumor grade (G1: 103% vs. G2: 85.8% vs. G3: 84.5%; p<0.05). In the non-malignant and malignant breast tissues, the expression levels of ESR1 and GPX1 were significantly correlated with each other (Rs=0.450 and Rs=0.360; respectively).
Our data suggest that down-regulation of ESR1 and GPX1 was independent of clinicopathological factors. Down-regulation of ESR1 gene expression was enhanced by the development of the disease. Moreover, GPX1 and ESR1 gene expression was interdependent in the malignant breast tissue and further work is needed to determine the mechanism underlying this relationship.
本研究的目的是确定雌激素受体α(由ESR1编码)的基因表达与肿瘤及邻近无肿瘤乳腺组织中谷胱甘肽过氧化物酶1(由GPX1编码)的表达是否相关,以及这种相关性是否受乳腺癌影响。这种关系可能会为雌激素受体状态下的乳腺癌病理学提供进一步的见解。
我们使用定量实时PCR技术分析乳腺癌患者配对的恶性和非恶性组织中ESR1和GPX1基因表达水平的差异。
与非恶性乳腺组织相比,肿瘤性乳腺组织中ESR1和GPX1的表达水平分别显著下调了14.7%和7.4%。这些基因的下调与肿瘤组织病理学分类和临床病理因素无关,而ESR1 mRNA水平随着肿瘤分级的增加而降低(G1:103% vs. G2:85.8% vs. G3:84.5%;p<0.05)。在非恶性和恶性乳腺组织中,ESR1和GPX1的表达水平彼此显著相关(分别为Rs=0.450和Rs=0.360)。
我们的数据表明,ESR1和GPX1的下调与临床病理因素无关。ESR1基因表达的下调因疾病发展而增强。此外,GPX1和ESR1基因表达在恶性乳腺组织中相互依赖,需要进一步研究以确定这种关系的潜在机制。