UOC Pediatric Oncology, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Rome, Italy.
Department of Pathology, Fondazione Policlinico Universitario A. Gemelli IRCCS, Catholic University of Sacred Heart, 00168 Rome, Italy.
Int J Mol Sci. 2021 Feb 13;22(4):1877. doi: 10.3390/ijms22041877.
Childhood ependymomas are heterogenous chemoresistant neoplasms arising from aberrant stem-like cells. Epigenome deregulation plays a pivotal role in ependymoma pathogenesis, suggesting that epigenetic modifiers hold therapeutic promise against this disease. Bromodomain and extraterminal domain (BET) proteins are epigenome readers of acetylated signals in histones and coactivators for oncogenic and stemness-related transcriptional networks, including MYC/MYCN (Proto-Oncogene, BHLH Transcritpion Factor)-regulated genes. We explored BET inhibition as an anticancer strategy in a panel of pediatric patient-derived ependymoma stem cell models by OTX015-mediated suppression of BET/acetylated histone binding. We found that ependymoma tissues and lines express BET proteins and their targets MYC and MYCN. In vitro, OTX015 reduced cell proliferation by inducing G0/G1-phase accumulation and apoptosis at clinically tolerable doses. Mechanistically, inhibitory p21 and p27 increased in a p53-independent manner, whereas the proliferative driver, phospho-signal transducer and activator of transcription 3 (STAT3), decreased. Upregulation of apoptosis-related proteins and survivin downregulation were correlated with cell line drug sensitivity. Minor alterations of MYC/MYCN expression were reported. In vivo, OTX015 significantly improved survival in 2/3 orthotopic ependymoma models. BET proteins represent promising targets for pharmaceutical intervention with OTX015 against ependymoma. The identification of predictive determinants of sensitivity may help identify ependymoma molecular subsets more likely to benefit from BET inhibitor therapies.
儿童室管膜瘤是一种异质性、耐药性的肿瘤,起源于异常的干细胞样细胞。表观基因组失调在室管膜瘤发病机制中起关键作用,这表明表观遗传修饰剂有望成为治疗这种疾病的方法。溴结构域和末端结构域(BET)蛋白是组蛋白乙酰化信号的表观基因组阅读器,也是致癌和干性相关转录网络的共激活因子,包括 MYC/MYCN(原癌基因,碱性螺旋-环-螺旋转录因子)调节基因。我们通过 OTX015 抑制 BET/乙酰化组蛋白结合,在一系列儿科患者来源的室管膜瘤干细胞模型中探索 BET 抑制作为一种抗癌策略。我们发现室管膜瘤组织和系表达 BET 蛋白及其靶标 MYC 和 MYCN。在体外,OTX015 在临床可耐受的剂量下通过诱导 G0/G1 期积累和细胞凋亡来减少细胞增殖。从机制上讲,抑制性 p21 和 p27 以不依赖 p53 的方式增加,而增殖驱动因子磷酸信号转导和转录激活因子 3(STAT3)减少。凋亡相关蛋白的上调和存活素的下调与细胞系药物敏感性相关。报道了 MYC/MYCN 表达的微小改变。在体内,OTX015 显著改善了 2/3 种原位室管膜瘤模型的存活率。BET 蛋白代表了使用 OTX015 针对室管膜瘤进行药物干预的有前途的靶点。预测敏感性的决定因素的确定可能有助于确定更有可能受益于 BET 抑制剂治疗的室管膜瘤分子亚群。