Anno2015
AutoriConigliaro A.; Costa V.; Lo Dico A.; Saieva L.; Buccheri S.; Dieli F.; Manno M.; Raccosta S.; Mancone C.; Tripodi M.; De Leo G.; Alessandro R.
AbstractBackground: CD90+ liver cancer cells have been described as cancer stem-cell-like (CSC), displaying aggressive and metastatic phenotype. Using two different in vitro models, already described as CD90+ liver cancer stem cells, our aim was to study their interaction with endothelial cells mediated by the release of exosomes. Methods: Exosomes were isolated and characterized from both liver CD90+ cells and hepatoma cell lines. Endothelial cells were treated with exosomes, as well as transfected with a plasmid containing the full length sequence of the long non-coding RNA (lncRNA) H19. Molecular and functional analyses were done to characterize the endothelial phenotype after treatments. Results: Exosomes released by CD90+ cancer cells, but not by parental hepatoma cells, modulated endothelial cells, promoting angiogenic phenotype and cell-to-cell adhesion. LncRNA profiling revealed that CD90+ cells were enriched in lncRNA H19, and released this through exosomes. Experiments of gain and loss of function of H19 showed that this LncRNA plays an important role in the exosome-mediated phenotype of endothelial cells. Conclusions: Our data indicate a new exosome-mediated mechanism by which CSC-like CD90+ cells could influence their tumor microenvironment by promoting angiogenesis. Moreover, we suggest the lncRNA H19 as a putative therapeutic target in hepatocellular carcinoma.
RivistaMolecular Cancer
ISSN1476-4598
Impact factor0
Volume14
Pagina inizio
Pagina fine
Autori IBFMauro MANNO, Samuele RACCOSTA
Linee di Ricerca IBFMD.P01.002.001
Sedi IBFIBF.PA