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甘草酸和甘草次酸对拓扑异构酶IIα的选择性作用以及与依托泊苷联合对三阴性乳腺癌MDA-MB-231细胞凋亡的影响

The selective effect of glycyrrhizin and glycyrrhetinic acid on topoisomerase IIα and apoptosis in combination with etoposide on triple negative breast cancer MDA-MB-231 cells.

作者信息

Cai Yun, Zhao Boxin, Liang Qianying, Zhang Yunqi, Cai Jieying, Li Guofeng

机构信息

Department of Pharmacy, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China; Rational Medication Evaluation and Drug Delivery Technology Lab, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.

Department of Pharmacy, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China; Rational Medication Evaluation and Drug Delivery Technology Lab, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China; Guangdong Key Laboratory of New Drug Screening, Southern Medical University, Guangzhou 510515, China.

出版信息

Eur J Pharmacol. 2017 Aug 15;809:87-97. doi: 10.1016/j.ejphar.2017.05.026. Epub 2017 May 12.

Abstract

Triple negative breast cancer(TNBC) has generated growing interests due to its aggressive biologic behavior and absence of targeted therapy approach. Glycyrrhizin(GL) from licorice root and its metabolite, glycyrrhetinic acid(GA) have shown extensive bioactivities in clinic. Here, we demonstrate that GL and GA have contrary anti-cancer effect on TNBC MDA-MB-231 cells. Beside its inhibition of cell proliferation, GA at non-cytotoxic concentration showed synergistic effect in combination with anti-cancer drug, etoposide(VP-16). Specifically, GA enhanced cytotoxicity through regulating topoisomerase IIα(TOPO 2A) targeted by etoposide. GA sensitized the cells to etoposide through elevating TOPO 2A with a 2.4 fold rate at 12h. From 12 to 48h, GA halved the expression of TOPO 2A and stimulated apoptosis, which exhibited its antineoplastic effect. Our experiments showed that GSH depletion, modulation of MAPK and AKT pathways accounted for the regulation of topoisomerase IIα and apoptosis. However, GL showed protection and detoxication by decreasing reactive oxygen species generation, maintaining GSH and differentially modulating apoptosis, AKT pathway, ERK and JNK of MAPK pathway. Collectively, our results demonstrate that GA, instead of GL, is a better candidate for TNBC treatment because of its anti-cancer effect and sensitization of topoisomerase IIα inhibitor.

摘要

三阴性乳腺癌(TNBC)因其侵袭性生物学行为以及缺乏靶向治疗方法而受到越来越多的关注。甘草根中的甘草酸(GL)及其代谢产物甘草次酸(GA)在临床上已显示出广泛的生物活性。在此,我们证明GL和GA对TNBC MDA-MB-231细胞具有相反的抗癌作用。除了抑制细胞增殖外,非细胞毒性浓度的GA与抗癌药物依托泊苷(VP-16)联合使用时显示出协同作用。具体而言,GA通过调节依托泊苷靶向的拓扑异构酶IIα(TOPO 2A)增强细胞毒性。GA在12小时时以2.4倍的速率升高TOPO 2A,从而使细胞对依托泊苷敏感。从12小时到48小时,GA使TOPO 2A的表达减半并刺激细胞凋亡,这显示了其抗肿瘤作用。我们的实验表明,谷胱甘肽耗竭、MAPK和AKT信号通路的调节是拓扑异构酶IIα和细胞凋亡调控的原因。然而,GL通过减少活性氧的产生、维持谷胱甘肽以及差异调节细胞凋亡、AKT信号通路、MAPK信号通路的ERK和JNK来发挥保护和解毒作用。总的来说,我们的结果表明,由于其抗癌作用和对拓扑异构酶IIα抑制剂的增敏作用,GA而非GL是TNBC治疗的更好候选药物。

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