Cytotoxic effects of neolignans from Saururus cernuus (Saururaceae) against prostate cancer cells

被引:0
|
作者
Toneto, Nicholas Pietro Agulha [1 ,2 ]
de Brito, Juliana Ribeiro [2 ]
Sartorelli, Patricia [2 ]
Uemi, Miriam [2 ]
Goncalves, Marina de Monroe
de Rubio, Ileana Gabriela Sanchez [1 ,2 ]
Lago, Joao Henrique Ghilardi [3 ]
Tamura, Rodrigo Esaki [1 ,2 ]
机构
[1] Univ Fed Sao Paulo, Lab Biol Mol Canc, Sao Paulo, Brazil
[2] Univ Fed Sao Paulo, Inst Ciencias Ambientais Quim & Farmaceut, Diadema, Brazil
[3] Univ Fed ABC, Ctr Ciencias Nat & Humanas, Santo Andre, Brazil
基金
巴西圣保罗研究基金会;
关键词
apoptosis; natural products; necrosis; neolignans; prostate cancer; Saururus cernuus; SAUCERNETIN-7; LIGNANS; CONSTITUENTS; APOPTOSIS;
D O I
10.1111/cbdd.14213
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 mu mol/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 mu mol/L and compound 2 showed effects at 100 mu mol/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.
引用
收藏
页码:1299 / 1306
页数:8
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