Kim Hyejeong Rosemary, Santhakumar Kirankumar, Markham Eleanor, Baldera Davide, Greenald David, Bryant Helen E, El-Khamisy Sherif F, van Eeden Fredericus J
Bateson Centre/BMS, Firth Court, University of Sheffield, Sheffield S10 2TN, UK.
Department of Genetic Engineering, SRM Institute of Science and Technology, Kattankulathur 603203, India.
Oncotarget. 2020 Mar 31;11(13):1109-1130. doi: 10.18632/oncotarget.27521.
pVHL is a tumor suppressor. The lack of its function leads to various tumors, among which ccRCC (clear cell renal cell carcinoma) has the most serious outcome due to its resistance to chemotherapies and radiotherapies. Although HIF promotes the progression of ccRCC, the precise mechanism by which the loss of VHL leads to tumor initiation remains unclear. We exploited two zebrafish mutants, and , and fish to identify crucial functions of Vhl in tumor initiation. Through the mutant analysis, we found that the role of pVHL in DNA repair is conserved in zebrafish Vll. Interestingly, we also discovered that Hif activation strongly suppressed genotoxic stress induced DNA repair defects and apoptosis in and mutants and in embryos lacking ATM activity. These results suggest the potential of HIF as a clinical modulator that can protect cells from accumulating DNA damage and apoptosis which can lead to cancers and neurodegenerative disorders.
pVHL是一种肿瘤抑制因子。其功能缺失会导致多种肿瘤,其中透明细胞肾细胞癌(ccRCC)由于对化疗和放疗具有抗性,后果最为严重。尽管缺氧诱导因子(HIF)促进ccRCC的进展,但VHL缺失导致肿瘤起始的确切机制仍不清楚。我们利用两种斑马鱼突变体以及野生型斑马鱼来确定Vhl在肿瘤起始中的关键功能。通过突变体分析,我们发现pVHL在DNA修复中的作用在斑马鱼Vll中是保守的。有趣的是,我们还发现Hif激活强烈抑制了基因毒性应激诱导的DNA修复缺陷以及在两种突变体和缺乏ATM活性的胚胎中的细胞凋亡。这些结果表明HIF作为一种临床调节剂的潜力,它可以保护细胞免受可能导致癌症和神经退行性疾病的DNA损伤积累和细胞凋亡。