Aim: to investigate the events involved in the progression of myxoid liposarcoma (MLS). Gene expression profiling and immunohistochemical/biochemical analyses were applied to specimens representative of the opposite ends of the MLS spectrum: pure myxoid (ML) and pure round cell (RC) liposarcomas. The analyses revealed the involvement of both coding and non coding RNAs (SNORDs located in DLK1-DIO3 region) and support a model of stepwise progression mainly driven by epigenetic changes involving tumour vascular supply and tumoral cellular component. In this model, a switch in the vascular landscape from a normal to a pro-angiogenic signature and the silencing of DLK1-DIO3 region mark the progression from ML to RC in concert with the acquisition by the latter of the overexpression of YY1/C-MYC/HDAC2, together with over-expression of genes involved in cell proliferation and stemness: MKNK2, MSX1 and TRIM71. Taken together, these findings strongly suggest that to progress from ML to RC liposarcoma the cells have to overcome the epigenetic silencing restriction point in order to reset their new stem-like differentiation signature. Our findings provide a first attempt at identifying the missing links between ML and RC liposarcomas, that may also have broader applications in other clinico-pathological settings characterised by a spectrum of progression.
Identification of a gene expression driven progression pathway in Myxoid liposarcoma / L. De Cecco, T. Negri, S. Brich, V. Mauro, F. Bozzi, G. Dagrada, V. Disciglio, R. Sanfilippo, A. Gronchi, N. Maurizio D'Incalci, P.G. Casali, S. Canevari, M.A. Pierotti, S. Pilotti. - In: ONCOTARGET. - ISSN 1949-2553. - 5:15(2014), pp. 5965-5977.
|Titolo:||Identification of a gene expression driven progression pathway in Myxoid liposarcoma|
|Parole Chiave:||myxoid liposarcoma; progression to round cell; gene expression array; epigenetic deregulation; stemness related genes; fast cell cycle related genes|
|Settore Scientifico Disciplinare:||Settore MED/06 - Oncologia Medica|
|Data di pubblicazione:||2014|
|Digital Object Identifier (DOI):||http://dx.doi.org/10.18632/oncotarget.2023|
|Appare nelle tipologie:||01 - Articolo su periodico|