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Arsenic trioxide inhibits Hedgehog, Notch and stem cell properties in glioblastoma neurospheres
- Source :
- Acta Neuropathologica Communications
- Publisher :
- Springer Nature
-
Abstract
- Background Notch and Hedgehog signaling have been implicated in the pathogenesis and stem-like characteristics of glioblastomas, and inhibitors of the pathways have been suggested as new therapies for these aggressive tumors. It has also been reported that targeting both pathways simultaneously can be advantageous in treating glioblastoma neurospheres, but this is difficult to achieve in vivo using multiple agents. Since arsenic trioxide has been shown to inhibit both Notch and Hedgehog in some solid tumors, we examined its effects on these pathways and on stem cell phenotype in glioblastoma. Results We found that arsenic trioxide suppresses proliferation and promotes apoptosis in three stem-like glioblastoma neurospheres lines, while inhibiting Notch and Hedgehog target genes. Importantly, arsenic trioxide markedly reduced clonogenic capacity of the tumor neurospheres, and the stem-like CD133-positive fraction was also diminished along with expression of the stem cell markers SOX2 and CD133. Conclusions Our results suggest that arsenic trioxide may be effective in targeting stem-like glioblastoma cells in patients by inhibiting Notch and Hedgehog activity.
- Subjects :
- Antineoplastic Agents
Apoptosis
Cell Growth Processes
Biology
Stem cell marker
Arsenicals
Pathology and Forensic Medicine
Colony-Forming Units Assay
Cellular and Molecular Neuroscience
chemistry.chemical_compound
Arsenic Trioxide
SOX2
Cell Line, Tumor
Neurosphere
Glial Fibrillary Acidic Protein
Humans
Hedgehog Proteins
Arsenic trioxide
Clonogenic assay
Hedgehog
neoplasms
Cell Proliferation
Dose-Response Relationship, Drug
Receptors, Notch
Research
Cell Cycle
Oxides
Flow Cytometry
Hedgehog signaling pathway
Cell biology
Gene Expression Regulation, Neoplastic
chemistry
embryonic structures
Neoplastic Stem Cells
Neurology (clinical)
Stem cell
Glioblastoma
Signal Transduction
Subjects
Details
- Language :
- English
- ISSN :
- 20515960
- Volume :
- 2
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Acta Neuropathologica Communications
- Accession number :
- edsair.doi.dedup.....e19a32dbedc9cd6cbc2a16940c316aad
- Full Text :
- https://doi.org/10.1186/2051-5960-2-31