Centre for Medicines Discovery, Nuffield Department of Medicine, University of Oxford, Oxford, OX3 7DQ, UK.
Cancer Research UK and Medical Research Council Oxford Institute for Radiation Oncology, Department of Oncology, University of Oxford, Oxford, OX3 7DQ, UK.
Cell Death Differ. 2022 Oct;29(10):1955-1969. doi: 10.1038/s41418-022-00983-4. Epub 2022 Apr 4.
Medulloblastoma is the most common malignant brain tumour in children. Genomic studies have identified distinct disease subgroups: wnt/wingless (WNT), sonic hedgehog (SHH), and non-WNT/non-SHH, comprising group 3 and group 4. Alterations in WNT and SHH signalling form the pathogenetic basis for their subgroups, whereas those for non-WNT/non-SHH tumours remain largely elusive. Recent analyses have revealed recurrent in-frame insertions in the E3 ubiquitin ligase adaptor Kelch Repeat and BTB Domain Containing 4 (KBTBD4) in cases of group 3/4 medulloblastoma. Critically, group 3/4 tumours with KBTBD4 mutations typically lack other gene-specific alterations, such as MYC amplification, indicating KBTBD4 insertion mutations as the primary genetic driver. Delineating the role of KBTBD4 mutations thus offers significant opportunities to understand tumour pathogenesis and to exploit the underpinning mechanisms therapeutically. Here, we show a novel mechanism in cancer pathogenesis whereby indel mutations in KBTBD4 drive its recognition of neo-substrates for degradation. We observe that KBTBD4 mutants promote the recruitment and ubiquitylation of the REST Corepressor (CoREST), which forms a complex to modulate chromatin accessibility and transcriptional programmes. The degradation of CoREST promoted by KBTBD4 mutation diverts epigenetic programmes inducing significant alterations in transcription to promote increased stemness of cancer cells. Transcriptional analysis of >200 human group 3 and 4 medulloblastomas by RNA-seq, highlights the presence of CoREST and stem-like signatures in tumours with KBTBD4 mutations, which extend to a further sub-set of non-mutant tumours, suggesting CoREST alterations as a novel pathogenetic mechanism of wide relevance in groups 3 and 4. Our findings uncover KBTBD4 mutation as a novel driver of epigenetic reprogramming in non-WNT/non-SHH medulloblastoma, establish a novel mode of tumorigenesis through gain-of-function mutations in ubiquitin ligases (neo-substrate recruitment) and identify both mutant KBTBD4 and CoREST complexes as new druggable targets for improved tumour-specific therapies.
髓母细胞瘤是儿童中最常见的恶性脑肿瘤。基因组研究已经确定了不同的疾病亚组:wnt/wingless(WNT)、sonic hedgehog(SHH)和非 WNT/非 SHH,包括第 3 组和第 4 组。WNT 和 SHH 信号通路的改变构成了它们亚组的发病基础,而对于非 WNT/非 SHH 肿瘤的改变在很大程度上仍然难以捉摸。最近的分析显示,在第 3/4 组髓母细胞瘤中,E3 泛素连接酶接头 Kelch Repeat 和 BTB 结构域包含 4(KBTBD4)中存在反复的框内插入。关键的是,具有 KBTBD4 突变的第 3/4 组肿瘤通常缺乏其他基因特异性改变,如 MYC 扩增,表明 KBTBD4 插入突变是主要的遗传驱动因素。因此,阐明 KBTBD4 突变的作用为理解肿瘤发病机制和利用潜在机制提供了重要机会。在这里,我们展示了一种新的癌症发病机制机制,其中 KBTBD4 的插入突变驱动其识别新的降解底物。我们观察到 KBTBD4 突变体促进 REST 核心抑制因子(CoREST)的募集和泛素化,该复合物形成复合物以调节染色质可及性和转录程序。KBTBD4 突变导致的 CoREST 降解会改变表观遗传程序,导致癌细胞的干性增加。通过 RNA-seq 对超过 200 个人类第 3 组和 4 组髓母细胞瘤进行的转录分析,突出了 KBTBD4 突变肿瘤中存在 CoREST 和干细胞样特征,这些特征扩展到进一步的非突变肿瘤亚组,提示 CoREST 改变作为第 3 组和第 4 组广泛相关的新发病机制机制。我们的发现揭示了 KBTBD4 突变是非 WNT/非 SHH 髓母细胞瘤中表观遗传重编程的新驱动因素,通过泛素连接酶的功能获得性突变(新底物募集)建立了一种新的肿瘤发生模式,并确定了突变的 KBTBD4 和 CoREST 复合物作为新的可药物靶标,以提高肿瘤特异性治疗效果。