Oral squamous cell carcinoma cancer stem cells have different drug sensitive to pharmacological NFκB and histone deacetylation inhibition

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Citações na Scopus
Tipo de produção
article
Data de publicação
2023
Título da Revista
ISSN da Revista
Título do Volume
Editora
E-CENTURY PUBLISHING CORP
Autores
SILVA, Luan Cesar
LEITE, Amanda Almeida
BORGATO, Gabriell Bonifacio
WAGNER, Vivian Petersen
MARTINS, Manoela Domingues
LOUREIRO, Felippe Jose Almeida
LOPES, Marcio Ajudarte
SANTOS-SILVA, Alan Roger
SPERANDIO, Marcelo
Citação
AMERICAN JOURNAL OF CANCER RESEARCH, v.13, n.12, p.6038-6050, 2023
Projetos de Pesquisa
Unidades Organizacionais
Fascículo
Resumo
Despite many progresses in the development of new systemic therapies for oral squamous cell carcinoma (OSCC), the five-year survival rate of OSCC is low. The traditional chemotherapies approach (cisplatin - CDDP) shows some limitations like drug toxicity, limited efficacy, and drug resistance. Promising studies suggested OSCC cancer stem cells (CSC) presented resistance to CDDP. We have previously studied many targets, and we extensively showed the efficacy of the NF kappa B signaling and the role of histones acetylation, on different malignant tumors, including adenoid cystic carcinoma and mucoepidermoid carcinoma, but until then the effects of the NFkB inhibitor and histone deacetylase (HDAC) inhibitor on the biology of OSCC were not evaluated. Here we assessed the pharmacological inhibitor of NF kappa B emetine and HDAC inhibitor SAHA on the behavior of CSC derived from OSCC. Our data suggested that CDDP administration resulted in reduced viability of bulk OSCC cells and increased CSC. A single and isolated shot of emetine and SAHA were able to disrupt CSC by inhibiting the NF kappa B pathway and increasing the histone acetylation levels, respectively. Further, the combined administration of emetine and SAHA presented the same CSC disruption as seen in emetine alone.
Palavras-chave
Head and neck tumors, oral squamous cell carcinoma, chemotherapy, target therapy, cancer stem cell
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