1. A case-control study of Metallothionein-1 expression in breast cancer and breast fibroadenoma.
- Author
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Sampaio FA, Martins LM, Dourado CSME, Revoredo CMS, Costa-Silva DR, Oliveira VA, Alves-Ribeiro FA, and Silva BBD
- Subjects
- Adult, Biomarkers, Tumor analysis, Breast metabolism, Breast pathology, Breast Neoplasms pathology, Case-Control Studies, Cross-Sectional Studies, Female, Fibroadenoma pathology, Humans, Middle Aged, Young Adult, Breast Neoplasms metabolism, Fibroadenoma metabolism, Metallothionein metabolism
- Abstract
The overexpression of Metallothionein-1 (MT-1) may play an important role in breast cancer; however, few studies have compared MT-1 expression between breast cancer and fibroadenoma. A cross-sectional controlled study was performed in 66 premenopausal women, aged 20-49 years, who had been histologically diagnosed with breast fibroadenoma or breast cancer. The patients were divided into two groups: group A, control (fibroadenoma, n = 36) and group B, study (breast cancer, n = 30). Immunohistochemistry was performed on tissue samples of fibroadenoma and breast cancer patients to evaluate the expression of metallothionein using an anti-MT-1 polyclonal antibody (rabbit polyclonal anti-metallothionein-Catalog Number biorbyt-orb11042) at a dilution of 1:100. The data were analyzed using NOVA (p < 0.05). Microscopic analysis showed a higher concentration of anti-MT-1-stained nuclei in breast cancer tissues than in fibroadenoma tissues. The mean proportion of cells with anti-MT-1-stained nuclei was 26.93% and 9.10%, respectively, in the study and control groups (p < 0.001). Histological grade 3 tumors showed a significantly higher MT-1 expression than hitological grade 1 (p < 0.05), while breast tumors negative for estrogen-, progesterone- and HER2- receptors had a significantly higher MT-1 expression than positive breast tumors positive for these parameters (p < 0.05). MT-1 protein in women of reproductive age was significantly higher in breast cancer than in fibroadenoma in this study. Furthermore, there was higher MT-1 immunoreactivity in more aggressive tumors.
- Published
- 2019
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