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.

IF 2.7 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Hsien-Kuo Chin, Mei-Chin Lu, Kai-Cheng Hsu, Mohamed El-Shazly, Tsen-Ni Tsai, Tzu-Yung Lin, Shou-Ping Shih, Tony Eight Lin, Zhi-Hong Wen, Yu-Chen S H Yang, Yi-Chang Liu
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引用次数: 0

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.

软珊瑚衍生的13-乙酰氧基石蜡内酯抗白血病作用的探索: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。
13-Acetoxysarcocrassolide (13-AC)是一种从水产养殖软珊瑚loophytum crassum中提取的海洋类胶质。13-AC对白血病细胞的细胞毒作用已有报道,但其作用机制尚不清楚。在本研究中,我们发现13-AC诱导人急性淋巴细胞白血病Molt4细胞凋亡,表现为PARP和caspases的裂解、磷脂酰丝氨酸外化以及线粒体膜电位的破坏。使用活性氧(ROS)清除剂n -乙酰半胱氨酸(NAC)可减弱13-AC诱导的细胞毒作用。分子对接和热移实验表明,13-AC的细胞毒作用机制可能是通过诱导Molt4细胞中热休克蛋白90 (hsp90)和拓扑异构酶i α的水平来抑制热休克蛋白90 (hsp90)的活性。13-AC还显示出强大的抗肿瘤活性,在体内Molt4异种移植小鼠模型中,其肿瘤体积(48.3%)和重量(72.5%)均减少。我们的研究结果表明,海洋类膜13-AC作为hsp90和拓扑异构酶IIα的双重抑制剂,通过增强ROS的产生发挥更有效的凋亡活性。
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来源期刊
Kaohsiung Journal of Medical Sciences
Kaohsiung Journal of Medical Sciences 医学-医学:研究与实验
CiteScore
5.60
自引率
3.00%
发文量
139
审稿时长
4-8 weeks
期刊介绍: Kaohsiung Journal of Medical Sciences (KJMS), is the official peer-reviewed open access publication of Kaohsiung Medical University, Taiwan. The journal was launched in 1985 to promote clinical and scientific research in the medical sciences in Taiwan, and to disseminate this research to the international community. It is published monthly by Wiley. KJMS aims to publish original research and review papers in all fields of medicine and related disciplines that are of topical interest to the medical profession. Authors are welcome to submit Perspectives, reviews, original articles, short communications, Correspondence and letters to the editor for consideration.
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