Design, Synthesis, and Anticancer Activity of Natural Product Hybrids With Paclitaxel Side Chain Inducing Apoptosis in Human Colon Cancer Cells

被引:4
|
作者
Zheng, Ling-Li [1 ]
Wen, Guan [2 ]
Yao, Yun-Xin [2 ]
Li, Xiao-Huan [2 ]
Gao, Feng [2 ]
机构
[1] Chengdu Med Coll, Afflicted Hosp 1, Dept Pharm, 278 Baoguang Rd, Chengdu 610500, Xindu Region, Peoples R China
[2] Southwest Jiaotong Univ, Sch Life Sci & Engn, Chengdu 610031, Peoples R China
基金
中国国家自然科学基金;
关键词
hybrid; paclitaxel; side chain; apoptosis; human colon cancer cells; NOVO CYTOTOXIC ALKALOIDS; BIOLOGICAL EVALUATION; BETA-TUBULIN; TAXOL; CONFORMATION; MIMICKING; MECHANISM; QUEST;
D O I
10.1177/1934578X20917298
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Based on the strong activity dependence of paclitaxel (PTX; Taxol) or docetaxel (Taxotere) on the C-13 side chain, a small library of dehydroepiandrosterone, cholesterol, vitamin D2, and alkaloids talatisamine and songorine-PTX hybrids have been synthesized and evaluated for in vitro anticancer activity by MTT assay against human breast (MCF-7), colon (HCT116), lung carcinoma (A549), and renal adenocarcinoma (786-0) cancer cell lines. Most hybrids (11b, 12b, 13b, 15b, and 18b) reduced the growth of MCF-7 and 786-0 cells with low PTX sensitivity in vitro. Among the synthesized compounds, hybrid 11b was better in inhibiting the growth of the 4 cells than PTX. A relatively low IC50 value of compound 11b (8.16 +/- 0.04 mu M) was also examined after exposure for 48 hours. Hybrid 11b showed a proapoptotic effect in HCT116 cells evaluated by Annexin V/propidium iodide binding assay. The level of hybrid 11b leading to protective cell death in HCT116 cells was detected using western blot and not easily observed in our basic examinations.
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页数:11
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