Back to Search
Start Over
Identification of genes involved in the biology of atypical teratoid/rhabdoid tumours using Drosophila melanogaster.
- Source :
-
Nature communications [Nat Commun] 2014 Jun 03; Vol. 5, pp. 4005. Date of Electronic Publication: 2014 Jun 03. - Publication Year :
- 2014
-
Abstract
- Atypical teratoid/rhabdoid tumours (AT/RT) are malignant brain tumours. Unlike most other human brain tumours, AT/RT are characterized by inactivation of one single gene, SMARCB1. SMARCB1 is a member of the evolutionarily conserved SWI/SNF chromatin remodelling complex, which has an important role in the control of cell differentiation and proliferation. Little is known, however, about the pathways involved in the oncogenic effects of SMARCB1 inactivation, which might also represent targets for treatment. Here we report a comprehensive genetic screen in the fruit fly that revealed several genes not yet associated with loss of snr1, the Drosophila homologue of SMARCB1. We confirm the functional role of identified genes (including merlin, kibra and expanded, known to regulate hippo signalling pathway activity) in human rhabdoid tumour cell lines and AT/RT tumour samples. These results demonstrate that fly models can be employed for the identification of clinically relevant pathways in human cancer.
- Subjects :
- Animals
Chromosomal Proteins, Non-Histone genetics
DNA-Binding Proteins genetics
Drosophila melanogaster
Gene Knockdown Techniques
Humans
Intracellular Signaling Peptides and Proteins genetics
Membrane Proteins genetics
Neurofibromin 2 genetics
Protein Serine-Threonine Kinases genetics
SMARCB1 Protein
Signal Transduction
Tumor Suppressor Proteins genetics
Brain Neoplasms genetics
Drosophila Proteins genetics
Rhabdoid Tumor genetics
Teratoma genetics
Transcription Factors genetics
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 5
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 24892285
- Full Text :
- https://doi.org/10.1038/ncomms5005