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β-环糊精/甘草酸功能化量子点选择性进入肝细胞并诱导细胞凋亡。

β-Cyclodextrin/glycyrrhizic acid functionalised quantum dots selectively enter hepatic cells and induce apoptosis.

机构信息

MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, P.R. China.

出版信息

Chemistry. 2012 Feb 6;18(6):1650-8. doi: 10.1002/chem.201102795. Epub 2012 Jan 2.

Abstract

The use of active components from important medical herbs has proved effective in treating various cancers. Glycyrrhizic acid (GA) is one of the many interesting triterpenoic acids with anticancerogenic potential, and is known to trigger apoptosis in hepatocarcinoma cells. In this study we combined quantum dots (QDs) with GA in the presence of β-cyclodextrin (β-CD), and prepared β-CD/GA-functionalised QDs, which led to improved antitumor activity and induced apoptosis in hepatocarcinoma cells. These compounds showed a better selectivity for hepatic cells compared to HeLa and ECV-304 cells. Hoechst and annexin V-FITC staining and mitochondrial membrane potential (MMP) experiments proved an apoptotic effect of these compounds on HepG2 cells. At the same time, transmission electron microscopy (TEM) showed obvious features of apoptosis, for example, irregularities of nuclear shapes, mitochondria swelling, clumping and peripheral chromatin condensation, zeiosis or blebbing of the plasma membrane and formation of apoptotic bodies. It is notable that β-CD/GA-functionalised QDs showed effective cell growth inhibition by triggering G0/G1 phase arrest and inducing apoptosis through an reactive oxygen species mediated mitochondrial dysfunction pathway. β-CD/GA-functionalised QDs primarily induced apoptotic response in a time- and dose-dependent manner, but little apoptosis appeared with L-Cys-β-CD-functionalised QDs or GA alone. These studies suggest that β-CD/GA-functionalised QDs have therapeutic potential against cancer.

摘要

从重要药用草本植物中提取的活性成分已被证明可有效治疗各种癌症。甘草酸(GA)是具有抗癌潜力的众多有趣三萜烯酸之一,已知可引发肝癌细胞凋亡。在这项研究中,我们在β-环糊精(β-CD)存在的情况下将量子点(QDs)与 GA 结合,制备了β-CD/GA 功能化的 QDs,这导致抗肿瘤活性提高,并诱导肝癌细胞凋亡。与 HeLa 和 ECV-304 细胞相比,这些化合物对肝细胞显示出更好的选择性。Hoechst 和 Annexin V-FITC 染色和线粒体膜电位(MMP)实验证明了这些化合物对 HepG2 细胞的凋亡作用。同时,透射电子显微镜(TEM)显示了这些化合物诱导 HepG2 细胞凋亡的明显特征,例如核形状不规则、线粒体肿胀、聚集和外周染色质浓缩、质膜起泡和凋亡小体形成。值得注意的是,β-CD/GA 功能化的 QDs 通过触发 G0/G1 期阻滞并通过活性氧介导的线粒体功能障碍途径诱导细胞凋亡,有效抑制细胞生长。β-CD/GA 功能化的 QDs 主要以时间和剂量依赖的方式诱导凋亡反应,但单独使用 L-Cys-β-CD 功能化的 QDs 或 GA 时几乎没有出现凋亡。这些研究表明,β-CD/GA 功能化的 QDs 具有治疗癌症的潜力。

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