Development of Ewing's sarcoma from primary bone marrow-derived mesenchymal progenitor cells.

Détails

ID Serval
serval:BIB_15B9430DD60D
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Development of Ewing's sarcoma from primary bone marrow-derived mesenchymal progenitor cells.
Périodique
Cancer research
Auteur⸱e⸱s
Riggi N., Cironi L., Provero P., Suvà M.L., Kaloulis K., Garcia-Echeverria C., Hoffmann F., Trumpp A., Stamenkovic I.
ISSN
0008-5472
Statut éditorial
Publié
Date de publication
2005
Peer-reviewed
Oui
Volume
65
Numéro
24
Pages
11459-68
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't - Publication Status: ppublish
Résumé
Ewing's sarcoma is a member of Ewing's family tumors (EFTs) and the second most common solid bone and soft tissue malignancy of children and young adults. It is associated in 85% of cases with the t(11;22)(q24:q12) chromosomal translocation that generates fusion of the 5' segment of the EWS gene with the 3' segment of the ETS family gene FLI-1. The EWS-FLI-1 fusion protein behaves as an aberrant transcriptional activator and is believed to contribute to EFT development. However, EWS-FLI-1 induces growth arrest and apoptosis in normal fibroblasts, and primary cells that are permissive for its putative oncogenic properties have not been discovered, hampering basic understanding of EFT biology. Here, we show that EWS-FLI-1 alone can transform primary bone marrow-derived mesenchymal progenitor cells and generate tumors that display hallmarks of Ewing's sarcoma, including a small round cell phenotype, expression of EFT-associated markers, insulin like growth factor-I dependence, and induction or repression of numerous EWS-FLI-1 target genes. These observations provide the first identification of candidate primary cells from which EFTs originate and suggest that EWS-FLI-1 expression may constitute the initiating event in EFT pathogenesis.
Mots-clé
Animals, Bone Marrow Cells, Cell Transformation, Neoplastic, Cyclin-Dependent Kinase Inhibitor p19, Fibroblasts, Gene Expression Profiling, Humans, Insulin-Like Growth Factor I, Mesenchymal Stem Cells, Mice, Mice, Inbred BALB C, Mice, SCID, Oligonucleotide Array Sequence Analysis, Oncogene Proteins, Fusion, Phenotype, Proto-Oncogene Protein c-fli-1, Sarcoma, Ewing's, Stem Cells, Tumor Markers, Biological, Tumor Suppressor Protein p53
Pubmed
Web of science
Open Access
Oui
Création de la notice
29/01/2008 18:34
Dernière modification de la notice
20/08/2019 12:44
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