Koeniger Anke, Polo Pierfrancesco, Brichkina Anna, Finkernagel Florian, Visekruna Alexander, Nist Andrea, Stiewe Thorsten, Daude Michael, Diederich Wibke E, Gress Thomas M, Adhikary Till, Lauth Matthias
Philipps University Marburg, Dept. of Gastroenterology, Endocrinology and Metabolism, Center for Tumor- and Immune Biology, 35043 Marburg, Germany.
Philipps University Marburg, Bioinformatics Core Facility, Center for Tumor- and Immune Biology, 35043 Marburg, Germany.
NAR Cancer. 2023 Feb 6;5(1):zcad007. doi: 10.1093/narcan/zcad007. eCollection 2023 Mar.
Transcriptional cancer subtypes which correlate with traits such as tumor growth, drug sensitivity or the chances of relapse and metastasis, have been described for several malignancies. The core regulatory circuits (CRCs) defining these subtypes are established by chromatin super enhancers (SEs) driving key transcription factors (TFs) specific for the particular cell state. In neuroblastoma (NB), one of the most frequent solid pediatric cancer entities, two major SE-directed molecular subtypes have been described: A more lineage-committed adrenergic (ADRN) and a mesenchymal (MES) subtype. Here, we found that a small isoxazole molecule (ISX), a frequently used pro-neural drug, reprogrammed SE activity and switched NB cells from an ADRN subtype towards a growth-retarded MES-like state. The MES-like state shared strong transcriptional overlap with ganglioneuroma (GN), a benign and highly differentiated tumor of the neural crest. Mechanistically, ISX suppressed chromatin binding of N-MYC, a CRC-amplifying transcription factor, resulting in loss of key ADRN subtype-enriched components such as N-MYC itself, PHOX2B and ALK, while concomitently, MES subtype markers were induced. Globally, ISX treatment installed a chromatin accessibility landscape typically associated with low risk NB. In summary, we provide evidence that CRCs and cancer subtype reprogramming might be amenable to future therapeutic targeting.
转录性癌症亚型与肿瘤生长、药物敏感性或复发及转移几率等特征相关,已在多种恶性肿瘤中有所描述。定义这些亚型的核心调控回路(CRC)由染色质超级增强子(SE)建立,SE驱动特定细胞状态所特有的关键转录因子(TF)。在神经母细胞瘤(NB)中,这是最常见的儿童实体瘤之一,已描述了两种主要的由SE指导的分子亚型:一种是更具谱系特异性的肾上腺素能(ADRN)亚型,另一种是间充质(MES)亚型。在此,我们发现一种常用的促神经药物——小异恶唑分子(ISX),可重新编程SE活性,并将NB细胞从ADRN亚型转变为生长迟缓的MES样状态。MES样状态与神经节神经瘤(GN)有很强的转录重叠,神经节神经瘤是一种神经嵴的良性且高度分化的肿瘤。从机制上讲,ISX抑制了N-MYC(一种CRC扩增转录因子)与染色质的结合,导致关键的ADRN亚型富集成分如N-MYC本身、PHOX2B和ALK丢失,同时诱导了MES亚型标志物。总体而言,ISX处理建立了一种通常与低风险NB相关的染色质可及性景观。总之,我们提供的证据表明,CRC和癌症亚型重编程可能适用于未来的治疗靶点。