Results

RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/citations/28525978http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/28525978http://www.w3.org/2000/01/rdf-schema#comment"

Background

Neuroblastoma is the most common extracranial solid malignancy in childhood, responsible for 15% of all pediatric cancer deaths. It is an heterogeneous disease that does not always respond to classical therapy; so the identification of new and specific molecular targets to improve existing therapy is needed. We have previously demonstrated the involvement of the Notch pathway in the onset and progression of neuroblastoma. In this study we further investigated the role of Notch signaling and identified Delta-like 1 (DLL1) as a novel molecular target in neuroblastoma cells with a high degree of MYCN amplification, which is a major oncogenic driver in neuroblastoma. The possibility to act on DLL1 expression levels by using microRNAs (miRNAs) was assessed.

Methods

DLL1 mRNA and protein expression levels were measured in three different neuroblastoma cell lines using quantitative real-time PCR and Western Blot analysis, respectively. Activation of the Notch pathway as a result of increased levels of DLL1 was analyzed by Immunofluorescence and Western Blot methods. In silico tools revealed the possibility to act on DLL1 expression levels with miRNAs, in particular with the miRNA-34 family. Neuroblastoma cells were transfected with miRNA-34 family members, and the effect of miRNAs transfection on DLL1 mRNA expression levels, on cell differentiation, proliferation and apoptosis was measured.

Results

In this study, the DLL1 ligand was identified as the Notch pathway component highly expressed in neuroblastoma cells with MYCN amplification. In silico analysis demonstrated that DLL1 is one of the targets of miRNA-34 family members that maps on chromosome regions that are frequently deregulated or deleted in neuroblastoma. We studied the possibility to use miRNAs to target DLL1. Among all miRNA-34 family members, miRNA-34b is able to significantly downregulate DLL1 mRNA expression levels, to arrest cell proliferation and to induce neuronal differentiation in malignant neuroblastoma cells.

Conclusions

Targeted therapies have emerged as new strategies for cancer treatment. This study identified the Notch ligand DLL1 as a novel and attractive molecular target in childhood neuroblastoma and its results could help to devise a targeted therapy using miRNAs."xsd:string
http://purl.uniprot.org/citations/28525978http://purl.org/dc/terms/identifier"doi:10.1186/s12885-017-3340-3"xsd:string
http://purl.uniprot.org/citations/28525978http://purl.uniprot.org/core/author"Memo M."xsd:string
http://purl.uniprot.org/citations/28525978http://purl.uniprot.org/core/author"Bettinsoli P."xsd:string
http://purl.uniprot.org/citations/28525978http://purl.uniprot.org/core/author"Bonini S.A."xsd:string
http://purl.uniprot.org/citations/28525978http://purl.uniprot.org/core/author"Ferrari-Toninelli G."xsd:string
http://purl.uniprot.org/citations/28525978http://purl.uniprot.org/core/author"Prandelli C."xsd:string
http://purl.uniprot.org/citations/28525978http://purl.uniprot.org/core/date"2017"xsd:gYear
http://purl.uniprot.org/citations/28525978http://purl.uniprot.org/core/name"BMC Cancer"xsd:string
http://purl.uniprot.org/citations/28525978http://purl.uniprot.org/core/pages"352"xsd:string
http://purl.uniprot.org/citations/28525978http://purl.uniprot.org/core/title"Notch ligand Delta-like 1 as a novel molecular target in childhood neuroblastoma."xsd:string
http://purl.uniprot.org/citations/28525978http://purl.uniprot.org/core/volume"17"xsd:string
http://purl.uniprot.org/citations/28525978http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/28525978
http://purl.uniprot.org/citations/28525978http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/28525978
http://purl.uniprot.org/uniprot/#_A0A384P5C6-mappedCitation-28525978http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/28525978
http://purl.uniprot.org/uniprot/#_O00548-mappedCitation-28525978http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/28525978
http://purl.uniprot.org/uniprot/A0A384P5C6http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/28525978
http://purl.uniprot.org/uniprot/O00548http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/28525978