Use este identificador para citar ou linkar para este item: http://hdl.handle.net/1843/77365
Tipo: Artigo de Periódico
Título: Inhibition of GATA3, ABCB1, and TYR by gallic acid: a real-world approach to uncovering a preventive agent against oral squamous cell carcinoma development
Autor(es): Osvaldo Sena Guimarães
Lílian Mendes Borburema Cangussu
Lorena dos Reis Pereira Queiroz
Eliane Macedo Sobrinho Santos
Marcela Gonçalves de Souza
Alfredo Maurício Batista de Paula
Lucyana Conceição Farias
Sérgio Henrique Sousa Santos
Marcos Flávio Silveira Vasconcelos D'Angelo
André Luiz Sena Guimarães
Resumo: Objective: this study aimed to the efficacy of gallic acid (GA) as a prospective prophylactic agent against the onset of oral squamous cell carcinoma (OSCC). Methods: we conducted bioinformatic analyses to identify the molecular targets of GA. Subsequently, we employed the 4NQO-induced animal model to evaluate the therapeutic potential of GA in OSCC. Results: our analysis unveiled that only three genes, ABCB1, GATA3, and SERPINE1, were associated with survival outcomes in OSCC patients. Reduced expressions of ABCB1 and GATA3 correlated with hazard ratios of 1.53 and 2.06, respectively, for mortality, while elevated SERPINE1 expression carried a 1.42-fold increased risk of death in OSCC patients. Molecular docking simulations underscored the robust affinity between GA and these genes, revealing binding energies of −6.0 kcal/mol for ABCB1, − 6.1 kcal/mol for GATA3, and −5.9 kcal/mol for SERPINE1. Furthermore, GA treatment demonstrated statistically significant reductions in the histopathological grade of 4NQO-induced lesions (p = 0.006) and mitigated liver (p < 0.001) and kidney (p < 0.001) toxicity associated with 4NQO exposure. Conclusion: the current study highlights GA as a promising contender for OSCC prevention. Mainly, GA targets critical genes such as ABCB1, GATA3, and SERPINE1, substantially impacting patient survival. Furthermore, GA administration mitigates 4NQO-induced toxicity, indicating its potential to improve animal survival by reducing lesion severity. These findings carry significant implications for OSCC research and potential clinical applications.
Assunto: Cabeça - Câncer
Pescoço - Câncer
Carcinoma de células escamosas
Ácido gálico
Polifenóis
Bioinformática
Idioma: eng
País: Brasil
Editor: Universidade Federal de Minas Gerais
Sigla da Instituição: UFMG
Departamento: ICA - INSTITUTO DE CIÊNCIAS AGRÁRIAS
Tipo de Acesso: Acesso Restrito
Identificador DOI: https://doi.org/10.1016/j.genrep.2023.101840
URI: http://hdl.handle.net/1843/77365
Data do documento: Dez-2023
metadata.dc.url.externa: https://www.sciencedirect.com/science/article/pii/S2452014423001024
metadata.dc.relation.ispartof: Gene Reports
Aparece nas coleções:Artigo de Periódico

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