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Molecular Dereplication and In Vitro and In Silico Pharmacological Evaluation of Coriandrum sativum against Neuroblastoma Cells.
Marcucci, Maria Cristina; Oliveira, Carlos Rocha; Spindola, Daniel; Antunes, Alyne A; Santana, Leila Y K; Cavalaro, Victor; Costa, Isabelle B; de Carvalho, Ana C; Veiga, Thiago A M; Medeiros, Livia S; Dos Santos Zamarioli, Lucas; Gonçalves, Carolina P; Santos, Milena F; Grecco, Simone S; Suzuki, Vanessa Y; Ferreira, Lydia Masako; Garcia, Daniel M.
Afiliação
  • Marcucci MC; Instituto de Ciência e Tecnologia, Universidade Estadual Paulista-UNESP, São José dos Campos 12231-280, SP, Brazil.
  • Oliveira CR; Grupo de Fitocomplexos e Sinalização Celular, Escola de Ciências da Saúde, Universidade Anhembi Morumbi, São Paulo 09972-270, SP, Brazil.
  • Spindola D; GAP Biotech, São José dos Campos 12231-280, SP, Brazil.
  • Antunes AA; Programa de Pós Graduação em Engenharia Biomédica, Universidade Federal de São Paulo, São José dos Campos 12231-280, SP, Brazil.
  • Santana LYK; Grupo de Fitocomplexos e Sinalização Celular, Escola de Ciências da Saúde, Universidade Anhembi Morumbi, São Paulo 09972-270, SP, Brazil.
  • Cavalaro V; Grupo de Fitocomplexos e Sinalização Celular, Escola de Ciências da Saúde, Universidade Anhembi Morumbi, São Paulo 09972-270, SP, Brazil.
  • Costa IB; Grupo de Fitocomplexos e Sinalização Celular, Escola de Ciências da Saúde, Universidade Anhembi Morumbi, São Paulo 09972-270, SP, Brazil.
  • de Carvalho AC; Grupo de Fitocomplexos e Sinalização Celular, Escola de Ciências da Saúde, Universidade Anhembi Morumbi, São Paulo 09972-270, SP, Brazil.
  • Veiga TAM; Grupo de Fitocomplexos e Sinalização Celular, Escola de Ciências da Saúde, Universidade Anhembi Morumbi, São Paulo 09972-270, SP, Brazil.
  • Medeiros LS; Departamento de Química, Universidade Federal de São Paulo, Diadema 09920-000, SP, Brazil.
  • Dos Santos Zamarioli L; Departamento de Química, Universidade Federal de São Paulo, Diadema 09920-000, SP, Brazil.
  • Gonçalves CP; Departamento de Química, Universidade Federal de São Paulo, Diadema 09920-000, SP, Brazil.
  • Santos MF; Grupo de Fitocomplexos e Sinalização Celular, Escola de Ciências da Saúde, Universidade Anhembi Morumbi, São Paulo 09972-270, SP, Brazil.
  • Grecco SS; Mestrado Profissional em Farmácia, Universidade Anhanguera de São Paulo, São Paulo 09972-270, SP, Brazil.
  • Suzuki VY; Mestrado Profissional em Farmácia, Universidade Anhanguera de São Paulo, São Paulo 09972-270, SP, Brazil.
  • Ferreira LM; Triplet Biotechnology Solutions, Bauru 17033-360, SP, Brazil.
  • Garcia DM; Programa de Pós Graduação em Cirurgia Translacional e Disciplina de Cirurgia Plástica, Escola Paulista de Medicina (EPM), Universidade Federal de São Paulo, São Paulo 09972-270, SP, Brazil.
Molecules ; 27(17)2022 Aug 24.
Article em En | MEDLINE | ID: mdl-36080159
The aim of this study was to investigate the cytotoxic activity of the Coriandrum sativum (C. sativum) ethanolic extract (CSEE) in neuroblastoma cells, chemically characterize the compounds present in the CSEE, and predict the molecular interactions and properties of ADME. Thus, after obtaining the CSEE and performing its chemical characterization through dereplication methods using UPLC/DAD-ESI/HRMS/MS, PM6 methods and the SwissADME drug design platform were used in order to predict molecular interactions and ADME properties. The CSEE was tested for 24 h in neuroblastoma cells to the establishment of the IC50 dose. Then, the cell death was evaluated, using annexin-PI, as well as the activity of the effector caspase 3, and the protein and mRNA levels of Bax and Bcl-2 were analyzed by ELISA and RT-PCR, respectively. By UHPLC/DAD/HRMS-MS/MS analysis, the CSEE showed a high content of isocoumarins-dihydrocoriandrin, coriandrin, and coriandrones A and B, as well as nitrogenated compounds (adenine, adenosine, and tryptophan). Flavonoids (apigenin, hyperoside, and rutin), phospholipids (PAF C-16 and LysoPC (16:0)), and acylglicerol were also identified in lower amount as important compounds with antioxidant activity. The in silico approach results showed that the compounds 1 to 6, which are found mostly in the C. sativum extract, obey the "Five Rules" of Lipinski, suggesting a good pharmacokinetic activity of these compounds when administered orally. The IC50 dose of CSEE (20 µg/mL) inhibited cell proliferation and promoted cell death by the accumulation of cleaved caspase-3 and the externalization of phosphatidylserine. Furthermore, CSEE decreased Bcl-2 and increased Bax, both protein and mRNA levels, suggesting an apoptotic mechanism. CSEE presents cytotoxic effects, promoting cell death. In addition to the promising results predicted through the in silico approach for all compounds, the compound 6 showed the best results in relation to stability due to its GAP value.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Coriandrum / Neuroblastoma Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Coriandrum / Neuroblastoma Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article