Department of Genetics, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, SP, Brazil.
Department of Pediatrics, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, SP, Brazil.
Cancer Gene Ther. 2020 Jun;27(6):509-512. doi: 10.1038/s41417-019-0122-x. Epub 2019 Jul 16.
RELA-fused supratentorial (ST) ependymoma (EPN) is an aggressive subgroup with poor prognosis. Considering the putative role of Notch signaling in the maintenance of the cancer stem cells (CSC) phenotype in RELA-fused EPN, we investigated the expression of Notch pathway and its target genes in this subgroup. We also evaluated the effects of two Notch inhibitors (DAPT and RO4929097) on cell proliferation, apoptosis, colony formation, and CSCs markers gene expression on EPN cell line of the RELA-fused subgroup (BXD-1425). In addition, in silico signatures of the Notch genes and CSCs markers were analyzed on a large clinical dataset from GSE64415 study. We found that among the ST-EPN subgroups the Notch signaling (NOTCH1, JAG1, JAG2, and HES4) is specifically activated in the ST-EPN-RELA. Furthermore, treatment of the RELA-fused EPN cell line with the Notch inhibitors impaired the Notch signaling expression and revealed that Notch axis is not essential for cell proliferation and survival in this setting. NOTCH1 expression in ST-EPN was correlated with the CSCs markers VEGFA and L1CAM overexpression and JAG1 expression was correlated with the CCND1 and CDK6 overexpression. In addition, in vitro treatment with Notch inhibitors induced downregulation of CSCs markers. These findings indicate that Notch signaling can be involved in the ST-EPN-RELA CSCs maintenance by modulating the expression of genes responsible for cell phenotype and cell fate.
RELA 融合型幕上室管膜瘤(EPN)是一种侵袭性亚组,预后不良。鉴于 Notch 信号通路在 RELA 融合型 EPN 中维持癌症干细胞(CSC)表型的假定作用,我们研究了该亚组中 Notch 通路及其靶基因的表达。我们还评估了两种 Notch 抑制剂(DAPT 和 RO4929097)对 RELA 融合型 EPN 细胞系(BXD-1425)细胞增殖、凋亡、集落形成和 CSCs 标记基因表达的影响。此外,我们还在 GSE64415 研究的大型临床数据集上分析了 Notch 基因和 CSCs 标记物的计算特征。我们发现,在 ST-EPN 亚组中,ST-EPN-RELA 中 Notch 信号(NOTCH1、JAG1、JAG2 和 HES4)特异性激活。此外,用 Notch 抑制剂处理 RELA 融合型 EPN 细胞系可削弱 Notch 信号表达,并表明在这种情况下 Notch 轴对于细胞增殖和存活不是必需的。ST-EPN 中的 NOTCH1 表达与 CSCs 标记物 VEGFA 和 L1CAM 的过表达相关,JAG1 表达与 CCND1 和 CDK6 的过表达相关。此外,体外用 Notch 抑制剂处理可诱导 CSCs 标记物下调。这些发现表明,Notch 信号通路可以通过调节负责细胞表型和细胞命运的基因的表达来参与 RELA 融合型 ST-EPN 的 CSCs 维持。