Phytochemical study and evaluation of cytotoxic and genotoxic properties of extracts from Clusia latipes leaves

被引:7
作者
Bailon-Moscoso, Natalia [1 ,2 ]
Romero-Benavides, Juan C. [3 ,4 ]
Sordo, Monserrat [1 ]
Villacis, Javier [2 ]
Silva, Ronald [4 ]
Celi, Luisa [2 ]
Martinez-Vazquez, Mariano [3 ]
Ostrosky-Wegman, Patricia [1 ]
机构
[1] Univ Nacl Autonoma Mexico, Dept Med Genom & Toxicol Ambiental, Inst Invest Biomed, Mexico City 04510, DF, Mexico
[2] Univ Tecn Particular Loja, Dept Ciencias Salud, Secc Genet Humana Microbiol & Bioquim Clin, Loja, Ecuador
[3] Univ Nacl Autonoma Mexico, Inst Quim, Mexico City 04510, DF, Mexico
[4] Univ Tecn Particular Loja, Dept Quim, Secc Quim Basica & Aplicada, Loja, Ecuador
来源
REVISTA BRASILEIRA DE FARMACOGNOSIA-BRAZILIAN JOURNAL OF PHARMACOGNOSY | 2016年 / 26卷 / 01期
关键词
Anti-cancer phytometabolites; Clusia latipes; Cytotoxicity; Genotoxicity; Comet assay; HESPERIDIN; CELLS; FRIEDELIN; BIPHENYL; PLANTS; MICE; SKIN;
D O I
10.1016/j.bjp.2015.08.014
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Some species of the Clusia genus have been shown to have important biomedical properties, including the ability to inhibit tumor growth in vitro and the usefulness for skin care. In this study, we examined the cytotoxic effect of hexane, ethyl acetate and methanol extracts from Clusia latipes Planch. & Triana, Clusiaceae, leaves on survival of human prostate cancer cells (PC-3), colon cancer cells (RKO), astrocytoma cells (D-384), and breast cancer cells (MCF-7). The ethyl acetate extract displayed the most substantial cytotoxic effect. However, using a Comet assay, we observed that the hexane extract induced a genotoxic effect (DNA damage) on human lymphocytes in an in vitro model. Chromatographic purification of the C. latipes hexane extract led to the isolation and identification of friedelin, friedolan-3-ol, and hesperidin as active cytotoxic compounds in hexane extract, while beta-amyrine was identified as an active cytotoxic compound in the ethyl acetate extract of C. latipes, thereby supporting further studies of the molecular mechanisms underlying the effect of these secondary metabolites on cancer cell survival. (C) 2015 Sociedade Brasileira de Farmacognosia. Published by Elsevier Editora Ltda. All rights reserved.
引用
收藏
页码:44 / 49
页数:6
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