芫花酮阻断线粒体自噬,促进mtDNA通过BAX-BAK1孔渗漏,抑制肝癌细胞增殖。

IF 4.4 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Frontiers in Pharmacology Pub Date : 2024-12-11 eCollection Date: 2024-01-01 DOI:10.3389/fphar.2024.1509482
Yan Qin, Ying Gao, Dan Wu, Qing-Qing Liu, Chang Su, Guan Liu, Le Yang, Ming-Gao Zhao, Jing-Yue Yao
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引用次数: 0

摘要

导论:肝细胞癌(HCC)是全球第三大致死癌症,其发病率呈上升趋势。HCC细胞中的线粒体容易受到代谢应激和氧化应激的损伤,因此需要加强线粒体自噬以维持线粒体稳态和细胞存活。因此,抑制线粒体自噬是一种很有前途的HCC治疗方法。中药臭椿酮已被证实可促进线粒体功能障碍,抑制肝癌。然而,其潜在机制尚不清楚。方法:采用CCK8法检测细胞增殖。采用JC-1、MitoTracker红/绿染色和MitoSOX染色检测线粒体稳态。ELISA和WB法分析炎症因子。采用线粒体和细胞质分离、基因组提取和qPCR检测线粒体DNA (mtDNA)渗漏。透射电镜观察线粒体超微结构。WB和IHC实验检测蛋白表达。免疫沉淀和免疫荧光成像检测蛋白-蛋白相互作用。通过异种移植小鼠模型验证了其体内抗肿瘤作用。结果:在本研究中,我们证实了臭椿酮抗肝癌的有效作用,并揭示了其分子机制。体外研究表明,臭椿酮可有效抑制PINK1-PRKN介导的线粒体自噬,并通过抑制PRKN促进BAX-BAK1线粒体孔的形成。这一过程导致线粒体mtDNA渗漏到细胞质中,随后引发炎症因子的诱导。抑制线粒体自噬和激活炎症反应最终导致HCC增殖抑制。体内研究表明,臭椿酮比5-氟尿嘧啶(5-FU)具有更强的抗hcc活性,且对动物体重和重要器官的生理功能无明显不良影响。结论:本研究强调了臭椿酮抗肝癌的作用,并阐明了其潜在的分子机制,提示臭椿酮治疗肝癌具有广阔的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ailanthone blocks mitophagy to promote mtDNA leakage through BAX-BAK1 pores and suppress hepatocellular carcinoma cell proliferation.

Introduction: Hepatocellular carcinoma (HCC), the third leading cancer mortality worldwide, shows rising incidence. The mitochondria in HCC cells are prone to damage from metabolic stress and oxidative stress, necessitating heightened mitophagy for mitochondrial homeostasis and cell survival. Thus, mitophagy inhibition is a promising HCC therapy. The traditional Chinese medicinal herb ailanthone have proved promote mitochondrial dysfunction and inhibits HCC. However, the underlying mechanism remains unclear.

Methods: CCK8 assay was applied to detect the proliferation. JC-1, MitoTracker Red/Green and MitoSOX staining were applied to detect the mitochondrial homeostasis. Inflammatory factors were analysed via ELISA and WB assay. Mitochondria and cytoplasm separation, genome extraction and qPCR were used to detect mitochondrial DNA (mtDNA) leakage. Mitochondria ultrastructure was detected by transmission electron microscopy. WB and IHC experiments were applied to detect protein expression. Protein-protein interactions detected by immunoprecipitation and immunofluorescence imaging. The in vivo antitumor effect was validated by the xenograft mouse model.

Results: In this study, we demonstrated the potent anti-HCC properties of ailanthone and revealed its molecular mechanism. In vitro studies demonstrated that ailanthone effectively inhibited PINK1-PRKN mediated mitophagy and promoted BAX-BAK1 mitochondrial pores formation through PRKN inhibition. This process led to the mitochondrial mtDNA leakage into the cytoplasm, which subsequently triggered the induction of inflammatory factors. The inhibition of mitophagy and the activation of inflammatory response ultimately led to HCC proliferation inhibition. In vivo studies demonstrated that ailanthone exhibited stronger anti-HCC activity than 5-Fluorouracil (5-FU), with no significant adverse effects on animal body weight or the physiological functions of vital organs.

Conclusion: This study highlighted the efficacy of ailanthone against HCC and elucidated its underlying molecular mechanisms, suggesting the promising therapeutic potential of ailanthone for HCC.

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来源期刊
Frontiers in Pharmacology
Frontiers in Pharmacology PHARMACOLOGY & PHARMACY-
CiteScore
7.80
自引率
8.90%
发文量
5163
审稿时长
14 weeks
期刊介绍: Frontiers in Pharmacology is a leading journal in its field, publishing rigorously peer-reviewed research across disciplines, including basic and clinical pharmacology, medicinal chemistry, pharmacy and toxicology. Field Chief Editor Heike Wulff at UC Davis is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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