Ouabain Effects on Human Anaplastic Thyroid Carcinoma 8505C Cells

Author:

Teixeira Mariana Pires,Haddad Natalia Ferreira,Passos Eliza Freitas,Andrade Marcelle Novaes,Campos Maria Luisa Arantes,da Silva Joyle Moreira Carvalho,de Figueiredo Camila SaggioroORCID,Giestal-de-Araujo Elizabeth,de Carvalho Denise PiresORCID,Miranda-Alves LeandroORCID,de Paiva Luciana Souza

Abstract

Anaplastic thyroid carcinoma (ATC) is a rare, but aggressive, carcinoma derived from follicular cells. While conventional treatments may improve patients’ survival, the lethality remains high. Therefore, there is an urgent need for more effective ATC treatments. Cardiotonic steroids, such as ouabain, have been shown to have therapeutic potential in cancer treatment. Thus, we aimed to evaluate ouabain’s effects in human anaplastic thyroid cells. For this, 8505C cells were cultured in the presence or absence of ouabain. Viability, cell death, cell cycle, colony formation and migratory ability were evaluated in ouabain-treated and control 8505C cells. The expression of differentiation and epithelial-to-mesenchymal transition (EMT) markers, as well as IL-6, TGFb1 and their respective receptors were also quantified in these same cells. Our results showed that ouabain in vitro decreased the number of viable 8505C cells, possibly due to an inhibition of proliferation. A reduction in migration was also observed in ouabain-treated 8505C cells. In contrast, decreased mRNA levels of PAX8 and TTF1 differentiation markers and increased levels of the N-cadherin EMT marker, as well as IL-6 and TGFb1, were found in ouabain-treated 8505C cells. In short, ouabain may have anti-proliferative and anti-migratory effect on 8505C cells, but maintains an aggressive and undifferentiated profile.

Funder

Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Pró-Reitoria de Pesquisa, Pós-Graduação e Inovação, Universidade Federal Fluminense

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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