Polybrominated diphenyl ethers BDE-47 and BDE-99 modulate murine melanoma cell phenotype in vitro
Autor: | Gisleine Jarenko Steil, Francisco Filipak Neto, João Luiz Aldinucci Buzzo, Ciro Alberto de Oliveira Ribeiro |
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Rok vydání: | 2021 |
Předmět: |
Chemistry
Health Toxicology and Mutagenesis Melanoma Multidrug resistance-associated protein 2 Polybrominated Biphenyls Cancer Cell migration General Medicine Tissue inhibitor of metalloproteinase medicine.disease Pollution Mice Phenotype Polybrominated diphenyl ethers Downregulation and upregulation Halogenated Diphenyl Ethers medicine Cancer research Animals Matrix Metalloproteinase 2 Environmental Chemistry Viability assay Flame Retardants |
Zdroj: | Environmental Science and Pollution Research. 29:11291-11303 |
ISSN: | 1614-7499 0944-1344 |
DOI: | 10.1007/s11356-021-16455-0 |
Popis: | Cancer is one of the leading causes of mortality worldwide. Even with the advances of pharmaceutical industry and treatments, the mortality rate for various types of cancer remains high. In particular, phenotypic alterations of tumor cells concerning drug efflux, migratory and invasive capabilities may represent a hurdle for cancer treatment and contribute to poor prognosis. In the present study, we investigated the effects of polybrominated diphenyl ethers (PBDEs) used as flame retardants on phenotypic features of melanoma cells that are important for cancer. Murine melanoma B16-F1 (less metastatic) and B16-F10 (more metastatic) cells were exposed to 0.01-1.0 nM of BDE-47 (2,2',4,4'-tetrabromodiphenyl ether), BDE-99 (2,2',4,4',5-pentabromodiphenyl ether), and the mixture of both (at 0.01 nM) for 24 h (acute exposure) and 15 days (chronic exposure). The polybrominated diphenyl ethers (PBDEs) did not affect cell viability but led to increased drug efflux transporter activity, cell migration, and colony formation, as well as overexpression of Abcc2 (ATP-binding cassette subfamily C member 2), Mmp-2 (matrix metalloproteinase-2), Mmp-9 (matrix metalloproteinase-9), and Tp53 (tumor protein p53) genes and downregulation of Timp-3 (tissue inhibitor of metalloproteinase 3) gene in B16-F10 cells. These effects are consistent with increased aggressiveness and malignancy of tumors due to exposure to the flame retardants and raise some concerns on the effects such chemicals may have on melanoma treatment and cancer prognosis. |
Databáze: | OpenAIRE |
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