{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Vera J"],"funding":["Agence Nationale de la Recherche","Fondation pour la Recherche Médicale","Ligue Nationale Contre le Cancer"],"pagination":["e10115"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC4733044"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["4"],"pubmed_abstract":["The PP2A phosphatase is often inactivated in cancer and is considered as a tumour suppressor. A new pathway controlling PP2A activity in mitosis has been recently described. This pathway includes the Greatwall (GWL) kinase and its substrates endosulfines. At mitotic entry, GWL is activated and phosphorylates endosulfines that then bind and inhibit PP2A. We analysed whether GWL overexpression could participate in cancer development. We show that GWL overexpression promotes cell transformation and increases invasive capacities of cells through hyperphosphorylation of the oncogenic kinase AKT. Interestingly, AKT hyperphosphorylation induced by GWL is independent of endosulfines. Rather, GWL induces GSK3 kinase dephosphorylation in its inhibitory sites and subsequent SCF-dependent degradation "],"journal":["eLife"],"pubmed_title":["Greatwall promotes cell transformation by hyperactivating AKT in human malignancies."],"pmcid":["PMC4733044"],"funding_grant_id":["SPF20111223514","ANR-10-BLAN-1207","LNCC LORCA 2014"],"pubmed_authors":["Soubeyran I","Vigneron S","Lartigue L","Del Rio M","Lorca T","Gadea G","Vera J","Castro A","Gire V","Chibon F"],"additional_accession":[]},"is_claimable":false,"name":"Greatwall promotes cell transformation by hyperactivating AKT in human malignancies.","description":"The PP2A phosphatase is often inactivated in cancer and is considered as a tumour suppressor. A new pathway controlling PP2A activity in mitosis has been recently described. This pathway includes the Greatwall (GWL) kinase and its substrates endosulfines. At mitotic entry, GWL is activated and phosphorylates endosulfines that then bind and inhibit PP2A. We analysed whether GWL overexpression could participate in cancer development. We show that GWL overexpression promotes cell transformation and increases invasive capacities of cells through hyperphosphorylation of the oncogenic kinase AKT. Interestingly, AKT hyperphosphorylation induced by GWL is independent of endosulfines. Rather, GWL induces GSK3 kinase dephosphorylation in its inhibitory sites and subsequent SCF-dependent degradation ","dates":{"release":"2015-01-01T00:00:00Z","publication":"2015 Nov","modification":"2025-04-19T20:30:53.006Z","creation":"2019-03-27T02:07:52Z"},"accession":"S-EPMC4733044","cross_references":{"pubmed":["26613407"],"doi":["10.7554/eLife.10115"]}}