Cowman Sophie, Pizer Barry, Sée Violaine
Institute of Systems, Molecular and Integrative Biology, Department of Molecular Physiology and Cell Signalling, University of Liverpool, Liverpool, Merseyside, United Kingdom.
Department of Pharmacology and Toxicology, College of Pharmacy, University of Utah, Salt-Lake-City, Utah, United States.
PeerJ. 2021 Apr 30;9:e11275. doi: 10.7717/peerj.11275. eCollection 2021.
Glioblastoma, a grade IV astrocytoma, has a poor survival rate in part due to ineffective treatment options available. These tumours are heterogeneous with areas of low oxygen levels, termed hypoxic regions. Many intra-cellular signalling pathways, including DNA repair, can be altered by hypoxia. Since DNA damage induction and subsequent activation of DNA repair mechanisms is the cornerstone of glioblastoma treatment, alterations to DNA repair mechanisms could have a direct influence on treatment success. Our aim was to elucidate the impact of chronic hypoxia on DNA repair gene expression in a range of glioblastoma cell lines. We adopted a NanoString transcriptomic approach to examine the expression of 180 DNA repair-related genes in four classical glioblastoma cell lines (U87-MG, U251-MG, D566-MG, T98G) exposed to 5 days of normoxia (21% O), moderate (1% O) or severe (0.1% O) hypoxia. We observed altered gene expression in several DNA repair pathways including homologous recombination repair, non-homologous end-joining and mismatch repair, with hypoxia primarily resulting in downregulation of gene expression. The extent of gene expression changes was dependent on hypoxic severity. Some, but not all, of these downregulations were directly under the control of HIF activity. For example, the downregulation of , a key component of non-homologous end-joining, was reversed upon inhibition of the hypoxia-inducible factor (HIF). In contrast, the downregulation of the mismatch repair gene, , was not affected by HIF inhibition. This suggests that numerous molecular mechanisms lead to hypoxia-induced reprogramming of the transcriptional landscape of DNA repair. Whilst the global impact of hypoxia on DNA repair gene expression is likely to lead to genomic instability, tumorigenesis and reduced sensitivity to anti-cancer treatment, treatment re-sensitising might require additional approaches to a simple HIF inhibition.
胶质母细胞瘤是一种IV级星形细胞瘤,其生存率较低,部分原因是可用的治疗方案效果不佳。这些肿瘤具有异质性,存在低氧区域,称为缺氧区域。许多细胞内信号通路,包括DNA修复,都可能因缺氧而改变。由于DNA损伤诱导和随后DNA修复机制的激活是胶质母细胞瘤治疗的基石,DNA修复机制的改变可能直接影响治疗效果。我们的目的是阐明慢性缺氧对一系列胶质母细胞瘤细胞系中DNA修复基因表达的影响。我们采用NanoString转录组学方法,检测了四种经典胶质母细胞瘤细胞系(U87-MG、U251-MG、D566-MG、T98G)在常氧(21% O₂)、中度(1% O₂)或重度(0.1% O₂)缺氧条件下暴露5天后180个DNA修复相关基因的表达。我们观察到包括同源重组修复、非同源末端连接和错配修复在内的几种DNA修复途径中的基因表达发生了改变,缺氧主要导致基因表达下调。基因表达变化的程度取决于缺氧的严重程度。其中一些(但不是全部)下调直接受缺氧诱导因子(HIF)活性的控制。例如,非同源末端连接的关键成分 的下调在缺氧诱导因子(HIF)受到抑制后得到逆转。相比之下,错配修复基因 的下调不受HIF抑制的影响。这表明多种分子机制导致缺氧诱导的DNA修复转录图谱重编程。虽然缺氧对DNA修复基因表达的整体影响可能导致基因组不稳定、肿瘤发生和对抗癌治疗的敏感性降低,但治疗再敏化可能需要除简单抑制HIF之外的其他方法。