新型蝎毒多肽 Androcin 18-1 通过诱导线粒体功能障碍对人类 U87 细胞显示出强大的抗肿瘤活性。

IF 3.2 2区 农林科学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Kai Wang , Tienthanh Nguyen , Yihan Gao , Ruiyin Guo , Chaofan Fan , Hang Liao , Jiali Li , Jinwei Chai , Xueqing Xu , Yuxin Gong , Xin Chen
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引用次数: 0

摘要

蝎毒具有多种抗癌成分,是开发抗肿瘤药物的有效天然来源。虽然已经从蝎毒 Androctonus bicolor 的转录组图谱中确定了 Androcin 18-1 的序列,但其生物活性仍不清楚。在这项研究中,我们描述了 Androcin 18-1 通过诱导人 U87 胶质母细胞瘤细胞膜破坏、ROS 积累和线粒体功能障碍来抑制细胞增殖和诱导细胞凋亡的抗肿瘤机制。此外,Androcin 18-1 还能通过细胞骨架紊乱和 MMPs/TIMPs 表达调控机制抑制细胞迁移。这项工作的发现凸显了 Androcin 18-1 在胶质母细胞瘤治疗药物开发中的潜在应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Androcin 18−1, a novel scorpion-venom peptide, shows a potent antitumor activity against human U87 cells via inducing mitochondrial dysfunction

Androcin 18−1, a novel scorpion-venom peptide, shows a potent antitumor activity against human U87 cells via inducing mitochondrial dysfunction

Androcin 18−1, a novel scorpion-venom peptide, shows a potent antitumor activity against human U87 cells via inducing mitochondrial dysfunction

Scorpion venom is a potent natural source for antitumor drug development due to the multiple action modes of anticancer components. Although the sequence of Androcin 18−1 has been identified from the transcriptome profile of the scorpion venom Androctonus bicolor, its bioactivity remains unclear. In this study, we described the antitumor mechanism whereby Androcin 18−1 inhibits the proliferation and induces apoptosis by inducing cell membrane disruption, ROS accumulation, and mitochondrial dysfunction in human U87 glioblastoma cells. Moreover, Androcin 18−1 could suppress cell migration via the mechanisms associated with cytoskeleton disorganization and MMPs/TIMPs expression regulation. The discovery of this work highlights the potential application of Androcin 18−1 in drug development for glioblastoma treatment.

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来源期刊
CiteScore
7.40
自引率
5.30%
发文量
105
审稿时长
40 days
期刊介绍: This international journal publishes original contributions and mini-reviews in the fields of insect biochemistry and insect molecular biology. Main areas of interest are neurochemistry, hormone and pheromone biochemistry, enzymes and metabolism, hormone action and gene regulation, gene characterization and structure, pharmacology, immunology and cell and tissue culture. Papers on the biochemistry and molecular biology of other groups of arthropods are published if of general interest to the readership. Technique papers will be considered for publication if they significantly advance the field of insect biochemistry and molecular biology in the opinion of the Editors and Editorial Board.
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