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从 Oplopanax horridus 中鉴定潜在的抗癌化合物。

Identification of potential anticancer compounds from Oplopanax horridus.

机构信息

Tang Center for Herbal Medicine Research, and Department of Anesthesia & Critical Care, University of Chicago, Chicago, IL 60637, USA.

出版信息

Phytomedicine. 2013 Aug 15;20(11):999-1006. doi: 10.1016/j.phymed.2013.04.013. Epub 2013 Jun 5.

Abstract

Oplopanax horridus is a plant native to North America. Previous reports have demonstrated that this herb has antiproliferative effects on cancer cells but study mostly focused on its extract or fractions. Because there has been limited phytochemical study on this herb, its bioactive compounds are largely unknown. We recently isolated and identified 13 compounds, including six polyynes, three sesquiterpenes, two steroids, and two phenolic acids, of which five are novel compounds. In this study, we systemically evaluated the anticancer effects of compounds isolated from O. horridus. Their antiproliferative effects on a panel of human colorectal and breast cancer cells were determined using the MTS assay. Cell cycle distribution and apoptotic effects were analyzed by flow cytometry. The in vivo antitumor effect was examined using a xenograft tumor model. Among the 13 compounds, strong antiproliferative effects were observed from falcarindiol and a novel compound oplopantriol A. Falcarindiol showed the most potent antiproliferative effects, significantly inducing pro-apoptosis and cell cycle arrest in the S and G2/M phases. The anticancer potential of falcarindiol was further verified in vivo, significantly inhibiting HCT-116 tumor growth in an athymic nude mouse model at 15 mg/kg. We also analyzed the relationship between polyyne structures and their pharmacological activities. We observed that both the terminal hydroxyl group and double bond obviously affected their anticancer potential. Results from this study supplied valuable information for future semi-synthesis of polyyne derivatives to develop novel cancer chemopreventive agents.

摘要

杠柳是一种原产于北美的植物。先前的报告表明,这种草药对癌细胞具有抗增殖作用,但研究主要集中在其提取物或馏分上。由于对这种草药的植物化学研究有限,其生物活性化合物在很大程度上是未知的。我们最近从杠柳中分离并鉴定了 13 种化合物,包括 6 种聚炔、3 种倍半萜、2 种甾体和 2 种酚酸,其中 5 种是新化合物。在这项研究中,我们系统地评估了杠柳中分离得到的化合物的抗癌作用。采用 MTS 法测定它们对一系列人结直肠和乳腺癌细胞的增殖抑制作用。通过流式细胞术分析细胞周期分布和凋亡作用。采用异种移植肿瘤模型检测体内抗肿瘤作用。在这 13 种化合物中,发现法卡林二醇和一种新化合物杠柳萜醇 A 具有很强的抗增殖作用。法卡林二醇表现出最强的抗增殖作用,显著诱导 S 和 G2/M 期的促凋亡和细胞周期停滞。法卡林二醇在体内的抗癌潜力也得到了进一步验证,在 15mg/kg 剂量下显著抑制了裸鼠模型中 HCT-116 肿瘤的生长。我们还分析了聚炔结构与其药理活性之间的关系。我们观察到,末端羟基和双键都明显影响它们的抗癌潜力。这项研究的结果为未来聚炔衍生物的半合成提供了有价值的信息,以开发新型癌症化学预防剂。

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