Epithelial splicing regulatory protein 1 (ESRP1) is an epithelial cell-specific RNA binding protein that controls several key cellular processes, like alternative splicing and translation. Previous studies have demonstrated a tumor suppressor role for this protein. Recently, however, a pro-metastatic function of ESRP1 has been reported. We thus aimed at clarifying the role of ESRP1 in Colorectal Cancer (CRC) by performing loss- and gain-of-function studies, and evaluating tumorigenesis and malignancy with in vitro and in vivo approaches. We found that ESRP1 plays a role in anchorage-independent growth of CRC cells. ESRP1-overexpressing cells grown in suspension showed enhanced fibroblast growth factor receptor (FGFR1/2) signalling, Akt activation, and Snail upregulation. Moreover, ESRP1 promoted the ability of CRC cells to generate macrometastases in mice livers. High ESRP1 expression may thus stimulate growth of cancer epithelial cells and promote colorectal cancer progression. Our findings provide mechanistic insights into a previously unreported, pro-oncogenic role for ESRP1 in CRC, and suggest that fine-tuning the level of this RNA-binding protein could be relevant in modulating tumor growth in a subset of CRC patients.

The RNA-binding protein ESRP1 promotes human colorectal cancer progression

FAGOONEE, SHARMILA;PICCO, GABRIELE;ORSO, FRANCESCA;LONGO, DARIO LIVIO;SCARFO', IRENE;CASSENTI, ADELE;PIVA, Roberto;CASSONI, Paola;SILENGO, Lorenzo;TOLOSANO, Emanuela;AIME, Silvio;TAVERNA, Daniela;PANDOLFI DE RINALDIS, Pier Paolo;BRANCACCIO, Mara;MEDICO, Enzo;ALTRUDA, Fiorella
Last
2017-01-01

Abstract

Epithelial splicing regulatory protein 1 (ESRP1) is an epithelial cell-specific RNA binding protein that controls several key cellular processes, like alternative splicing and translation. Previous studies have demonstrated a tumor suppressor role for this protein. Recently, however, a pro-metastatic function of ESRP1 has been reported. We thus aimed at clarifying the role of ESRP1 in Colorectal Cancer (CRC) by performing loss- and gain-of-function studies, and evaluating tumorigenesis and malignancy with in vitro and in vivo approaches. We found that ESRP1 plays a role in anchorage-independent growth of CRC cells. ESRP1-overexpressing cells grown in suspension showed enhanced fibroblast growth factor receptor (FGFR1/2) signalling, Akt activation, and Snail upregulation. Moreover, ESRP1 promoted the ability of CRC cells to generate macrometastases in mice livers. High ESRP1 expression may thus stimulate growth of cancer epithelial cells and promote colorectal cancer progression. Our findings provide mechanistic insights into a previously unreported, pro-oncogenic role for ESRP1 in CRC, and suggest that fine-tuning the level of this RNA-binding protein could be relevant in modulating tumor growth in a subset of CRC patients.
2017
8
6
10007
10024
http://www.impactjournals.com/oncotarget/index.php?journal=oncotarget&page=article&op=download&path%5B%5D=14318&path%5B%5D=45670
ESRP1; Human colorectal cancer; Proto-oncogene; RNA binding protein; Oncology
Fagoonee, Sharmila; Picco, Gabriele; Orso, Francesca; Arrigoni, Arrigo; Longo, Dario L.; Forni, Marco; Scarfò, Irene; Cassenti, Adele; Piva, Roberto; Cassoni, Paola; Silengo, Lorenzo; Tolosano, Emanuela; Aime, Silvio; Taverna, Daniela; Pandolfi, Pier Paolo; Brancaccio, Mara; Medico, Enzo; Altruda, Fiorella
File in questo prodotto:
File Dimensione Formato  
Fagonee.pdf

Accesso aperto

Descrizione: ARTICOLO PRINCIPALE
Tipo di file: PDF EDITORIALE
Dimensione 5.13 MB
Formato Adobe PDF
5.13 MB Adobe PDF Visualizza/Apri
5_fagoonee.pdf

Accesso riservato

Tipo di file: PDF EDITORIALE
Dimensione 933.13 kB
Formato Adobe PDF
933.13 kB Adobe PDF   Visualizza/Apri   Richiedi una copia

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1633280
Citazioni
  • ???jsp.display-item.citation.pmc??? 37
  • Scopus 52
  • ???jsp.display-item.citation.isi??? 50
social impact