Brain Tumour Research Centre, Institute of Biological and Biomedical Sciences, School of Pharmacy and Biomedical Sciences, University of Portsmouth, Portsmouth PO1 2DT, UK.
Centre for Enzyme Innovation, Institute of Biological and Biomedical Sciences, School of Biological Sciences, University of Portsmouth, Portsmouth PO1 2DY, UK.
Int J Mol Sci. 2019 Jul 9;20(13):3364. doi: 10.3390/ijms20133364.
Glioblastoma is the most common and malignant primary brain tumour in adults, with a dismal prognosis. This is partly due to considerable inter- and intra-tumour heterogeneity. Changes in the cellular energy-producing mitochondrial respiratory chain complex (MRC) activities are a hallmark of glioblastoma relative to the normal brain, and associate with differential survival outcomes. Targeting MRC complexes with drugs can also facilitate anti-glioblastoma activity. Whether mutations in the mitochondrial DNA (mtDNA) that encode several components of the MRC contribute to these phenomena remains underexplored. We identified a germ-line mtDNA mutation (m. 14798T > C), enriched in glioblastoma relative to healthy controls, that causes an amino acid substitution F18L within the core mtDNA-encoded cytochrome b subunit of MRC complex III. F18L is predicted to alter corresponding complex III activity, and sensitivity to complex III-targeting drugs. This could in turn alter reactive oxygen species (ROS) production, cell behaviour and, consequently, patient outcomes. Here we show that, despite a heterogeneous mitochondrial background in adult glioblastoma patient biopsy-derived cell cultures, the F18L substitution associates with alterations in individual MRC complex activities, in particular a 75% increase in MRC complex II_III activity, and a 34% reduction in CoQ10, the natural substrate for MRC complex III, levels. Downstream characterisation of an F18L-carrier revealed an 87% increase in intra-cellular ROS, an altered cellular distribution of mitochondrial-specific ROS, and a 64% increased sensitivity to clomipramine, a repurposed MRC complex III-targeting drug. In patients, F18L-carriers that received the current standard of care treatment had a poorer prognosis than non-carriers (373 days vs. 415 days, respectively). Single germ-line mitochondrial mutations could predispose individuals to differential prognoses, and sensitivity to mitochondrial targeted drugs. Thus, F18L, which is present in blood could serve as a useful non-invasive biomarker for the stratification of patients into prognostically relevant groups, one of which requires a lower dose of clomipramine to achieve clinical effect, thus minimising side-effects.
胶质母细胞瘤是成人中最常见和最恶性的原发性脑肿瘤,预后较差。这在一定程度上是由于肿瘤内和肿瘤间存在相当大的异质性。与正常大脑相比,细胞能量产生的线粒体呼吸链复合物(MRC)活性的变化是胶质母细胞瘤的一个标志,并与不同的生存结果相关。用药物靶向 MRC 复合物也可以促进抗胶质母细胞瘤的活性。线粒体 DNA(mtDNA)中的突变是否会导致 MRC 的几个成分发生这种现象仍未得到充分探索。我们发现了一种种系 mtDNA 突变(m.14798T>C),它在胶质母细胞瘤中相对于健康对照富集,导致 MRC 复合物 III 中线粒体编码细胞色素 b 亚基的核心 mtDNA 编码的 F18L 氨基酸取代。F18L 预计会改变相应的复合物 III 活性和对复合物 III 靶向药物的敏感性。这反过来又会改变活性氧(ROS)的产生、细胞行为,进而改变患者的预后。在这里,我们表明,尽管在成人胶质母细胞瘤患者活检衍生细胞培养物中有一个异质性的线粒体背景,但 F18L 取代与个别 MRC 复合物活性的改变有关,特别是 MRC 复合物 II_III 活性增加了 75%,而 MRC 复合物 III 的天然底物 CoQ10 水平降低了 34%。对 F18L 携带者的下游特征分析显示,细胞内 ROS 增加了 87%,线粒体特异性 ROS 的细胞分布发生改变,对氯米帕明的敏感性增加了 64%,氯米帕明是一种重新定位的 MRC 复合物 III 靶向药物。在患者中,接受当前标准治疗的 F18L 携带者的预后比非携带者差(分别为 373 天和 415 天)。单一的种系线粒体突变可能使个体易患不同的预后,并对线粒体靶向药物敏感。因此,存在于血液中的 F18L 可以作为一种有用的非侵入性生物标志物,用于将患者分层为具有预后相关性的组,其中一组需要较低剂量的氯米帕明才能达到临床效果,从而最大程度地减少副作用。