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探讨软珊瑚源 13-乙酰基软珊瑚内酯的抗白血病作用:通过氧化应激诱导细胞凋亡,作为热休克蛋白 90 和拓扑异构酶 II 的有效抑制剂。

Exploration of anti-leukemic effect of soft coral-derived 13-acetoxysarcocrassolide: Induction of apoptosis via oxidative stress as a potent inhibitor of heat shock protein 90 and topoisomerase II.

机构信息

Department of Marine Biotechnology and Resources, National Sun Yat-Sen University, Kaohsiung, Taiwan.

Division of Cardiovascular Surgery, Department of Surgery, Kaohsiung Armed Forces General Hospital, Kaohsiung, Taiwan.

出版信息

Kaohsiung J Med Sci. 2023 Jul;39(7):718-731. doi: 10.1002/kjm2.12678. Epub 2023 Apr 13.

Abstract

13-Acetoxysarcocrassolide (13-AC) is a marine cembranoid derived from the aquaculture soft coral of Lobophytum crassum. The cytotoxic effect of 13-AC against leukemia cells was previously reported but its mechanism of action is still unexplored. In the current study, we showed that 13-AC induced apoptosis of human acute lymphoblastic leukemia Molt4 cells, as evidenced by the cleavage of PARP and caspases, phosphatidylserine externalization, as well as the disruption of mitochondrial membrane potential. The use of N-acetylcysteine (NAC), a reactive oxygen species (ROS) scavenger, attenuated the cytotoxic effect induced by 13-AC. Molecular docking and thermal shift assay indicated that the cytotoxic mechanism of action of 13-AC involved the inhibition of heat shock protein 90 (Hsp 90) activity by eliciting the level of Hsp 70 and topoisomerase IIα in Molt4 cells. 13-AC also exhibited potent antitumor activity by reducing the tumor volume (48.3%) and weight (72.5%) in the in vivo Molt4 xenograft mice model. Our findings suggested that the marine cembranoid, 13-AC, acted as a dual inhibitor of Hsp 90 and topoisomerase IIα, exerting more potent apoptotic activity via the enhancement of ROS generation.

摘要

13-乙酰基鲨烯内酯(13-AC)是一种来源于养殖软珊瑚 Lobophytum crassum 的海洋枞烷类化合物。先前已有报道称 13-AC 对白血病细胞具有细胞毒性作用,但作用机制尚不清楚。在本研究中,我们表明 13-AC 诱导人急性淋巴细胞白血病 Molt4 细胞凋亡,证据为 PARP 和半胱天冬酶的裂解、磷脂酰丝氨酸外翻以及线粒体膜电位的破坏。使用 N-乙酰半胱氨酸(NAC),一种活性氧(ROS)清除剂,可减弱 13-AC 诱导的细胞毒性作用。分子对接和热移位测定表明,13-AC 的细胞毒性作用机制涉及通过引发 Molt4 细胞中 HSP70 和拓扑异构酶 IIα 的水平来抑制热休克蛋白 90(Hsp90)的活性。13-AC 还通过减少体内 Molt4 异种移植小鼠模型中的肿瘤体积(48.3%)和重量(72.5%)表现出强大的抗肿瘤活性。我们的研究结果表明,海洋枞烷类化合物 13-AC 作为 Hsp90 和拓扑异构酶 IIα 的双重抑制剂,通过增强 ROS 的产生发挥更强的促凋亡活性。

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