Your browser doesn't support javascript.
loading
Cytotoxic effects of neolignans from Saururus cernuus (Saururaceae) against prostate cancer cells.
Toneto, Nicholas Pietro Agulha; de Brito, Juliana Ribeiro; Sartorelli, Patricia; Uemi, Miriam; Gonçalves, Marina de Monroe; de Rubio, Ileana Gabriela Sánchez; Lago, João Henrique Ghilardi; Tamura, Rodrigo Esaki.
Afiliação
  • Toneto NPA; Laboratório de Biologia Molecular do Câncer, Universidade Federal de São Paulo, São Paulo, Brazil.
  • de Brito JR; Instituto de Ciências Ambientais, Químicas e Farmacêuticas, Universidade Federal de São Paulo, Diadema, Brazil.
  • Sartorelli P; Instituto de Ciências Ambientais, Químicas e Farmacêuticas, Universidade Federal de São Paulo, Diadema, Brazil.
  • Uemi M; Instituto de Ciências Ambientais, Químicas e Farmacêuticas, Universidade Federal de São Paulo, Diadema, Brazil.
  • Gonçalves MM; Instituto de Ciências Ambientais, Químicas e Farmacêuticas, Universidade Federal de São Paulo, Diadema, Brazil.
  • de Rubio IGS; Centro de Ciências Naturais e Humanas, Universidade Federal do ABC, Santo Andre, Brazil.
  • Lago JHG; Laboratório de Biologia Molecular do Câncer, Universidade Federal de São Paulo, São Paulo, Brazil.
  • Tamura RE; Instituto de Ciências Ambientais, Químicas e Farmacêuticas, Universidade Federal de São Paulo, Diadema, Brazil.
Chem Biol Drug Des ; 101(6): 1299-1306, 2023 06.
Article em En | MEDLINE | ID: mdl-36752700
ABSTRACT
In this study, five neolignans were isolated from Saururus cernuus-threo-dihydroguaiaretic acid (1), threo-austrobailignan-6 (2), threo-austrobailignan-5 (3), verrucosin (4), and saucernetin (5)-and have their cytotoxic effects evaluated in prostate cancer cell lines (PC3 and DU145). Initially, using an in silico approach, tested compounds were predicted to be absorbed by the gastrointestinal tract, be able to permeate the blood-brain barrier and did not show any alert in PAINS (pan-assay structures interference). In vitro assays showed that compounds 2, 4, and 5 reduced cell viability of DU145 cell line at 100 µmol/L after 48 h while compounds 1 and 3 showed to be inactive at the same conditions. Furthermore, compounds 4 and 5 reduced cell number as early as in 24 h at 50 µmol/L and compound 2 showed effects at 100 µmol/L in 24 h against both cancer cell lines PC3 and DU145. Studies using flow cytometry were conducted and indicated that compound 4 induced strong necrosis and apoptosis whereas compound 5 induced strong necrosis. Otherwise, less active compound 2 did not show evidence of induction of apoptosis or necrosis, suggesting that its mechanism of action involves inhibition of cell proliferation. In conclusion, compounds 4 and 5 have been shown to be promising cytotoxic agents against prostate cancer cell lines and can be used as a starting point for the development of new drugs for the treatment of prostate cancer.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Lignanas / Saururaceae / Antineoplásicos Limite: Humans / Male Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Lignanas / Saururaceae / Antineoplásicos Limite: Humans / Male Idioma: En Ano de publicação: 2023 Tipo de documento: Article