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靶向 FACT 的库尔沙因药物 CBL0137 有效抑制 MYC 扩增型 3 组髓母细胞瘤。

Effective inhibition of MYC-amplified group 3 medulloblastoma by FACT-targeted curaxin drug CBL0137.

机构信息

Department of Pediatric Neurosurgery, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, People's Republic of China.

Key Laboratory of Cell Differentiation and Apoptosis of National Ministry of Education, Department of Pathophysiology, Shanghai Jiao Tong University School of Medicine, Shanghai, People's Republic of China.

出版信息

Cell Death Dis. 2020 Dec 2;11(12):1029. doi: 10.1038/s41419-020-03201-6.

Abstract

Medulloblastoma (MB) is the most common malignant pediatric brain tumor that can be categorized into four major molecular subgroups. Group 3 MB with MYC amplification (MYCamp-G3-MB) has been shown to be highly aggressive and exhibited worst prognosis, indicating the need for novel effective therapy most urgently. A few epigenetic targeted therapeutic strategies have recently been proven to effectively treat preclinical models of MYCamp-G3-MB, including BET inhibition, HDAC inhibition and SETD8 inhibition, unveiling a promising direction for further investigation. In this study, we carried out systemic bioinformatic analyses of public-available MB datasets as well as functional genomic screening datasets of primary MYCamp-G3-MB lines to search for other potential therapeutic targets within epigenetic modulators. We identified SSRP1, a subunit of histone-chaperone FACT complex, to be the top drug target candidate as it is highly cancer-dependent in whole-genome CRISPR-Cas9 screening across multiple MYCamp-G3-MB lines; significantly upregulated in MYCamp-G3-MB compared to normal cerebellum and most of the rest MB subtypes; its higher expression is correlated with worse prognosis; and it has a blood-brain-barrier penetrable targeted drug that has entered early phase human clinical trials already. Then we utilized RNA-interference approach to verify the cancer-dependency of SSRP1 in multiple MYCamp-G3-MB lines and further confirmed the therapeutic efficacy of FACT-targeted curaxin drug CBL0137 on treating preclinical models of MYCamp-G3-MB in vitro and in vivo, including an orthotopic intracranial xenograft model. Mechanistically, transcriptome analyses showed CBL0137 preferentially suppressed cell-cycle and DNA-repair related biological processes. Moreover, it selectively disrupted transcription of MYC and NEUROD1, two critical oncogenic transcription factors of MYCamp-G3-MB, via depleting FACT complex from their promoter regions. In summary, our study demonstrates FACT-targeted CBL0137 works effectively on treating MYCamp-G3-MB, presenting another promising epigenetic-targeted therapeutic strategy against the most devastating form of MB.

摘要

髓母细胞瘤(MB)是最常见的小儿恶性脑肿瘤,可分为四个主要分子亚群。MYC 扩增的组 3 MB(MYCamp-G3-MB)已被证明具有高度侵袭性和最差的预后,这表明最迫切需要新的有效治疗方法。最近,一些表观遗传靶向治疗策略已被证明可有效治疗 MYCamp-G3-MB 的临床前模型,包括 BET 抑制、HDAC 抑制和 SETD8 抑制,为进一步研究开辟了有希望的方向。在这项研究中,我们对公共可用的 MB 数据集以及原发性 MYCamp-G3-MB 系的功能基因组筛选数据集进行了系统的生物信息学分析,以在表观遗传调节剂中寻找其他潜在的治疗靶点。我们确定 SSRP1 是组蛋白伴侣 FACT 复合物的一个亚基,作为顶级药物靶点候选物,因为它在多个 MYCamp-G3-MB 系的全基因组 CRISPR-Cas9 筛选中高度依赖于癌症;与正常小脑和大多数其他 MB 亚型相比,在 MYCamp-G3-MB 中显著上调;其较高的表达与预后较差相关;并且已经有一种可穿透血脑屏障的靶向药物进入了早期人体临床试验。然后,我们利用 RNA 干扰方法在多个 MYCamp-G3-MB 系中验证了 SSRP1 的癌症依赖性,并进一步证实了靶向 FACT 的 curaxin 药物 CBL0137 在体外和体内治疗 MYCamp-G3-MB 临床前模型的疗效,包括原位颅内异种移植模型。从机制上讲,转录组分析表明 CBL0137 优先抑制细胞周期和 DNA 修复相关的生物学过程。此外,它通过从其启动子区域耗尽 FACT 复合物,选择性地抑制 MYC 和 NEUROD1(MYCamp-G3-MB 的两个关键致癌转录因子)的转录。总之,我们的研究表明,靶向 FACT 的 CBL0137 可有效治疗 MYCamp-G3-MB,为治疗最具破坏性形式的 MB 提供了另一种有前途的表观遗传靶向治疗策略。

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