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.
引用
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页数:11
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