Apoptosis inducing activity of benzophenanthridine-type alkaloids and 2-arylbenzofuran neolignans in HCT116 colon carcinoma cells

被引:39
作者
Mansoor, Tayyab A. [1 ,2 ]
Borralho, Pedro M. [1 ,3 ]
Luo, Xuan [1 ,2 ]
Mulhovo, Silva [4 ]
Rodrigues, Cecilia M. P. [1 ,3 ]
Ferreira, Maria-Jose U. [1 ,2 ]
机构
[1] Univ Lisbon, Fac Pharm, Res Inst Med & Pharmaceut Sci IMed UL, P-1649003 Lisbon, Portugal
[2] Univ Lisbon, Fac Pharm, Dept Pharmaceut & Med Chem, P-1649003 Lisbon, Portugal
[3] Univ Lisbon, Fac Pharm, Dept Biochem & Human Biol, P-1649003 Lisbon, Portugal
[4] Univ Pedag, Ctr Estudos Mocambicanos & Etnociencias, Maputo 21402161, Mozambique
关键词
Apoptosis; Cytotoxicity; HCT116 colon carcinoma cells; Benzophenanthridine alkaloids; Arylbenzofuran neolignans; Zanthoxylum capense; MULTIDRUG-RESISTANCE; CANCER-CELLS; INDUCTION; LIGNANS; PRODUCTS; INDUCERS; PLANTS;
D O I
10.1016/j.phymed.2013.03.026
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Thirteen compounds belonging to different classes of alkaloids (1-9) and lignans (10-13), isolated from the methanol extract of roots of the African medicinal plant Zanthoxylum capense, were assayed for their ability as apoptosis inducers in HCT116 colon carcinoma cells. The cytotoxicity of these compounds was evaluated in HCT116 colon carcinoma cells by the MTS assay. Out of the tested compounds, three benzophenanthridine alkaloids (1,4, and 7), a dibenzyl butyrolactone lignan (10), and two 2-arylbenzofuran neolignans (12 and 13) displayed significant cytotoxicity to HCT116 cells, confirmed by the Guava Via-Count viability assay. The selected compounds (1, 4, 7, 10, 12, and 13) were further tested for apoptosis induction activity in HCT116 cells, by evaluation of nuclear morphology following Hoechst staining, and by caspase-3 like activity assays. Morphologic evaluation of HCT116 nuclei following Hoechst staining and fluorescence microscopy revealed that compounds 1,4, 7,10, 12, and 13 induced apoptosis in HCT116 colon carcinoma cells, producing similar, or higher, apoptosis levels when compared with 5-fluorouracil (5-FU), the cornerstone cytotoxic used in colon cancer treatment for several decades. In fact, HCT116 cells developed morphological changes characteristic of apoptosis, including chromatin condensation, nuclear fragmentation and formation of apoptotic bodies. Importantly, compounds 4 and 13 at 20 mu M were the most promising in this study, inducing respectively similar to 11- and 7-fold increases in apoptotic cells as compared to vehicle control, whereas 5-FU increased apoptosis by similar to 2-fold. Apoptosis induction for compounds 4 and 13 was further confirmed by caspase-3-like activity assays, which showed respectively similar to 2- and 1.5-fold increases in caspase-3-like activity compared to vehicle control. These results suggested that specific benzophenanthridine alkaloids and 2-arylbenzofuran neolignans isolated from Zanthoxylum capense show strong anticancer activity in HCT116 colon carcinoma cells. (C) 2013 Elsevier GmbH. All rights reserved.
引用
收藏
页码:923 / 929
页数:7
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