4.6 Article

Notch pathway in ependymoma RELA-fused subgroup: upregulation and association with cancer stem cells markers expression

Journal

CANCER GENE THERAPY
Volume 27, Issue 6, Pages 509-512

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41417-019-0122-x

Keywords

-

Funding

  1. Fundação de Amparo à Pesquisa do Estado de São Paulo (São Paulo Research Foundation) [2014/20341-0] Funding Source: Medline
  2. Ministry of Science, Technology and Innovation | Conselho Nacional de Desenvolvimento Científico e Tecnológico (National Council for Scientific and Technological Development) [457884/2014-2, 151760/2018-7] Funding Source: Medline
  3. Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (Brazilian Federal Agency for the Support and Evaluation of Graduate Education) [Finance Code 001] Funding Source: Medline

Ask authors/readers for more resources

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, andHES4) 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.NOTCH1expression in ST-EPN was correlated with the CSCs markersVEGFAandL1CAMoverexpression andJAG1expression was correlated with theCCND1andCDK6overexpression. 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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available