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Autor(es):
Cordeiro, Helon Guimaraes ; de Sousa Faria, Alessandra Valeria ; Ferreira-Halder, Carmen Verissima
Número total de Autores: 3
Tipo de documento: Artigo Científico
Fonte: Biological Chemistry; v. 401, n. 9, p. 7-pg., 2020-08-01.
Resumo

Colorectal Cancer (CRC) therapy confronts challenges as chemoresistance and side effects. Therefore, drugs with antitumor properties that downmodulate aggressiveness mediators are required. Studies have shown the relevance of Low Molecular Weight Protein Tyrosine Phosphatase (LMWPTP), Protein Tyrosine Phosphatase 1B (PTP1B), and Transforming Growth Factor ss (TGF ss) in mediating proliferation, chemoresistance, and metastasis. In this study, we aimed to investigate the responsiveness of colorectal cancer lines (HT29 and HCT116) towards Vemurafenib and whether this treatment could modulate these aggressiveness mediators. Cytotoxicity Assays (MTT and Trypan Exclusion Test) were performed to evaluate the viability of HT29 and HCT116 cells treated with Vemurafenib. Western blotting was performed to analyze the amount and/or the activity of mediators (LMWPTP, PTP1B, TGF ss, SMAD3), and the immunoprecipitation was performed to evaluate LMWPTP activity. This study brought up novel aspects of Vemurafenib action in colorectal cancer, which can decrease the activity of protein tyrosine phosphatases (LMWPTP and PTP1B) and the TGF ss pathway, making them important in the CRC aggressiveness. By downmodulating colorectal cancer hallmarks, Vemurafenib appears as an interesting candidate for CRC therapeutic protocols. (AU)

Processo FAPESP: 15/20412-7 - Proteína tirosina fosfatase de baixo peso molecular em câncer de cólon retal: da bancada à geração de produto
Beneficiário:Carmen Veríssima Ferreira
Modalidade de apoio: Auxílio à Pesquisa - Temático
Processo FAPESP: 17/08119-8 - Primeira etapa da disseminação hematogênica de células de câncer de cólon retal: influência da LMWPTP e do 3-bromopiruvato
Beneficiário:Alessandra Valéria de Sousa Faria
Modalidade de apoio: Bolsas no Brasil - Doutorado