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来自鳄梨的新型抗癌烯内酯。

Novel anticancer alkene lactone from Persea americana.

机构信息

Institute of Chemistry, University of Rostock, 18059 Rostock, Germany.

出版信息

Pharm Biol. 2013 Jun;51(6):700-6. doi: 10.3109/13880209.2013.764326. Epub 2013 Apr 9.

DOI:10.3109/13880209.2013.764326
PMID:23570517
Abstract

CONTEXT

Persea americana Mill (Lauraceae) root bark is used in ethnomedicine for a variety of diseases including cancer.

OBJECTIVE

To isolate and characterize the chemical constituent in P. americana, and also to determine the anticancer property of a new alkene lactone from the root bark of P. americana.

MATERIALS AND METHODS

The MCF-7 cells were treated with different concentrations of the pure compound for 48 h. The percentage of cells in the various phases, online monitoring of metabolic changes and integrin receptor expression determined by flow cytometry.

RESULTS

One novel alkene lactone (4-hydroxy-5-methylene-3-undecyclidenedihydrofuran-2 (3H)-one) (1) was isolated and characterized using 1D-NMR, 2D-NMR, infrared, UV and MS. At a concentration of 10 µg/mL, significant reduction of proliferation of MCF-7 was induced while MCF-12 A cell was significantly stimulated by 10 µg/mL. The IC50 value for MCF-7 cells is 20.48 µg/mL. Lower concentration of 1 harbor no significant effect on either MCF-7 or MCF-12A. The apoptotic rates of MCF-7 cells were increased significantly. At the final concentration 10 µg/mL, up to 80% of all breast cancer cells were dead. On the non-tumorigenic cell line MCF-12A, the same concentrations (1 and 10 µg/mL) of compound 1 caused significant enhanced apoptotic rates. A total of 1 µg/mL of 1 caused a decrease of α4-, α6-, β1- and β3-integrin expression.

CONCLUSIONS

The compound caused a stimulatory effect on non-tumorigenic MCF-12A cells with respect to cell adhesion while tumorigenic MCF-7 cells detached continuously. This is the first report on the anticancer effects of this class of compound.

摘要

背景

鳄梨(樟科)根皮在传统医学中用于治疗多种疾病,包括癌症。

目的

从鳄梨根皮中分离和鉴定化学成分,并确定一种新的烯内酯的抗癌特性。

材料和方法

用不同浓度的纯化合物处理 MCF-7 细胞 48 小时。通过流式细胞术检测细胞在不同阶段的比例、在线监测代谢变化和整合素受体表达。

结果

用 1D-NMR、2D-NMR、红外、UV 和 MS 鉴定并描述了一种新的烯内酯(4-羟基-5-亚甲基-3-十一环二氢呋喃-2(3H)-酮)(1)。在 10μg/mL 浓度下,MCF-7 的增殖显著减少,而 MCF-12A 细胞则被 10μg/mL 显著刺激。MCF-7 细胞的 IC50 值为 20.48μg/mL。浓度低于 1 时,对 MCF-7 或 MCF-12A 均无明显影响。MCF-7 细胞的凋亡率显著增加。在终浓度为 10μg/mL 时,高达 80%的乳腺癌细胞死亡。在非致瘤细胞系 MCF-12A 中,相同浓度(1 和 10μg/mL)的化合物 1 导致凋亡率显著增加。1μg/mL 的化合物 1 导致α4、α6、β1 和β3 整合素表达降低。

结论

该化合物对非致瘤性 MCF-12A 细胞的细胞黏附具有刺激作用,而致瘤性 MCF-7 细胞则不断分离。这是该类化合物抗癌作用的首次报道。

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