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线粒体阻滞剂-6导致的线粒体损伤抑制肝癌细胞增殖。

Mitochondrial Impairment by MitoBloCK-6 Inhibits Liver Cancer Cell Proliferation.

作者信息

Kabiri Yaschar, Fuhrmann Anna, Becker Anna, Jedermann Luisa, Eberhagen Carola, König Ann-Christine, Silva Tiago Barros, Borges Fernanda, Hauck Stefanie M, Michalke Bernhard, Knolle Percy, Zischka Hans

机构信息

Institute of Toxicology and Environmental Hygiene, School of Medicine, Technical University of Munich, Munich, Germany.

Institute of Molecular Toxicology and Pharmacology, Helmholtz Center Munich, German Research Center for Environmental Health, Neuherberg, Germany.

出版信息

Front Cell Dev Biol. 2021 Sep 20;9:725474. doi: 10.3389/fcell.2021.725474. eCollection 2021.

Abstract

Augmenter of liver regeneration (ALR) is a critical multi-isoform protein with its longer isoform, located in the mitochondrial intermembrane space, being part of the mitochondrial disulfide relay system (DRS). Upregulation of was observed in multiple forms of cancer, among them hepatocellular carcinoma (HCC). To shed light into ALR function in HCC, we used MitoBloCK-6 to pharmacologically inhibit ALR, resulting in profound mitochondrial impairment and cancer cell proliferation deficits. These effects were mostly reversed by supplementation with bioavailable hemin b, linking ALR function to mitochondrial iron homeostasis. Since many tumor cells are known for their increased iron demand and since increased iron levels in cancer are associated with poor clinical outcome, these results help to further advance the intricate relation between iron and mitochondrial homeostasis in liver cancer.

摘要

肝脏再生增强因子(ALR)是一种关键的多异构体蛋白,其较长的异构体位于线粒体内膜间隙,是线粒体二硫键中继系统(DRS)的一部分。在多种癌症中均观察到ALR的上调,其中包括肝细胞癌(HCC)。为了阐明ALR在肝癌中的功能,我们使用MitoBloCK-6从药理学上抑制ALR,导致严重的线粒体损伤和癌细胞增殖缺陷。补充生物可利用的血红素b大多可逆转这些效应,将ALR的功能与线粒体铁稳态联系起来。由于许多肿瘤细胞以其增加的铁需求而闻名,并且由于癌症中铁水平的升高与不良临床结果相关,这些结果有助于进一步推进肝癌中铁与线粒体稳态之间的复杂关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac0c/8488156/29f7e1c783ca/fcell-09-725474-g001.jpg

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