Human glioblastoma is the most frequent and aggressive form of brain tumour in the adult population. Proteolytic turnover of tumour suppressors by the ubiquitin-proteasome system is a mechanism that tumour cells can adopt to sustain their growth and invasiveness. However, the identity of ubiquitin-proteasome targets and regulators in glioblastoma are still unknown. Here we report that the RING ligase praja2 ubiquitylates and degrades Mob, a core component of NDR/LATS kinase and a positive regulator of the tumour-suppressor Hippo cascade. Degradation of Mob through the ubiquitin-proteasome system attenuates the Hippo cascade and sustains glioblastoma growth in vivo. Accordingly, accumulation of praja2 during the transition from low- to high-grade glioma is associated with significant downregulation of the Hippo pathway. These findings identify praja2 as a novel upstream regulator of the Hippo cascade, linking the ubiquitin proteasome system to deregulated glioblastoma growth.

Proteolysis of MOB1 by the ubiquitin ligase praja2 attenuates Hippo signalling and supports glioblastoma growth / Lignitto, L; Arcella, A; Sepe, M; Rinaldi, Laura; DELLE DONNE, Rossella; Gallo, A; Stefan, E; Bachmann, Va; Oliva, Ma; Tiziana Storlazzi, C; L'Abbate, A; Brunetti, Arturo; Gargiulo, Sara; Gramanzini, M; Insabato, Luigi; Garbi, Corrado; Gottesman, Me; Feliciello, Antonio. - In: NATURE COMMUNICATIONS. - ISSN 2041-1723. - 4:1822(2013), pp. 1-13. [10.1038/ncomms2791]

Proteolysis of MOB1 by the ubiquitin ligase praja2 attenuates Hippo signalling and supports glioblastoma growth.

RINALDI, LAURA;DELLE DONNE, ROSSELLA;BRUNETTI, ARTURO;GARGIULO, SARA;INSABATO, LUIGI;GARBI, CORRADO;FELICIELLO, ANTONIO
2013

Abstract

Human glioblastoma is the most frequent and aggressive form of brain tumour in the adult population. Proteolytic turnover of tumour suppressors by the ubiquitin-proteasome system is a mechanism that tumour cells can adopt to sustain their growth and invasiveness. However, the identity of ubiquitin-proteasome targets and regulators in glioblastoma are still unknown. Here we report that the RING ligase praja2 ubiquitylates and degrades Mob, a core component of NDR/LATS kinase and a positive regulator of the tumour-suppressor Hippo cascade. Degradation of Mob through the ubiquitin-proteasome system attenuates the Hippo cascade and sustains glioblastoma growth in vivo. Accordingly, accumulation of praja2 during the transition from low- to high-grade glioma is associated with significant downregulation of the Hippo pathway. These findings identify praja2 as a novel upstream regulator of the Hippo cascade, linking the ubiquitin proteasome system to deregulated glioblastoma growth.
2013
Proteolysis of MOB1 by the ubiquitin ligase praja2 attenuates Hippo signalling and supports glioblastoma growth / Lignitto, L; Arcella, A; Sepe, M; Rinaldi, Laura; DELLE DONNE, Rossella; Gallo, A; Stefan, E; Bachmann, Va; Oliva, Ma; Tiziana Storlazzi, C; L'Abbate, A; Brunetti, Arturo; Gargiulo, Sara; Gramanzini, M; Insabato, Luigi; Garbi, Corrado; Gottesman, Me; Feliciello, Antonio. - In: NATURE COMMUNICATIONS. - ISSN 2041-1723. - 4:1822(2013), pp. 1-13. [10.1038/ncomms2791]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/574236
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