Methylmercury promotes breast cancer cell proliferation

• Published in: Toxicology reports Vol. 5; pp. 579 - 584
• Main Authors: Gaudet, Hilary M., Christensen, Emily, Conn, Brandon, Morrow, Sara, Cressey, Lauren, Benoit, Janina
• Format: Journal Article
• Language: English
• Published: Ireland Elsevier B.V 01.01.2018; Elsevier
• Subjects: Breast cancer; Mercury; Metalloestrogen; Methylmercury; Breast cancer; Mercury; Metalloestrogen; Methylmercury
• ISSN: 2214-7500; 2214-7500
• DOI: 10.1016/j.toxrep.2018.05.002

[Display omitted] •More mercury is retained in cell supernatant when exposed in full versus minimal media.•More mercury associates with cells exposed in minimal media compared to full media.•Less mercury promotes breast cancer cell proliferation when exposed in minimal media. Metalloestrogens are small ionic metals that activate the estrogen receptor (ER). Studies have shown that when metalloestrogens bind to the ER, there is an increase in transcription and expression of estrogen-regulated genes, which induces proliferation of estrogen-dependent breast cancer. Methylmercury (MeHg), a metalloestrogen, is present in the environment and is toxic at moderate to high concentrations. However, at lower concentrations MeHg may promote the proliferation of ER-positive breast cancers and protect cells against pro-apoptotic signals. To investigate the effects of MeHg treatment on breast cancer cells in vitro. MCF7 breast cancer cells were treated with concentrations of MeHg ranging from 1 nM to 100 mM. Hg analysis was used to quantify intracellular mercury concentrations. Cell proliferation and apoptosis were determined by cell counting and Annexin-V staining, respectively. We defined a protocol that maximizes cellular exposure to mercury. Treatment of human ER-positive breast cancer cells with 1 nM MeHg promoted proliferation, while treatment with a concentration of 100 nM induced apoptosis. Clarifying the effects of MeHg on breast cancer will improve our understanding of how environmental toxins affect tumor progression and may lead to the development of future therapeutic strategies.