English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/219358
Share/Impact:
Statistics
logo share SHARE logo core CORE   Add this article to your Mendeley library MendeleyBASE

Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL
Exportar a otros formatos:

Title

Downregulation of specific FBXW7 isoforms with differential effects in T-cell lymphoblastic lymphoma

AuthorsVázquez-Domínguez, Irene; González-Sánchez, Laura ; López-Nieva, Pilar ; Fernandez-Navarro, Pablo; Villa-Morales, María ; Cobos-Fernández, María A.; Sastre, Isabel ; Fraga, Mario F.; Fernandez, Agustín F; Malumbres, Marcos; Salazar-Roa, María; Graña-Castro, Osvaldo; Santos, Javier ; Llamas, Pilar; López-Lorenzo, José L.; Fernández-Piqueras, José
Issue Date11-Feb-2019
CitationOncogene (2019)
AbstractFBXW7 is a driver gene in T-cell lymphoblastic neoplasia acting through proteasome degradation of key proto-oncogenes. FBXW7 encodes three isoforms, α, β and γ, which differ only in the N-terminus. In this work, massive sequencing revealed significant downregulation of FBXW7 in a panel of primary T-cell lymphoblastic lymphomas characterised by the absence of mutations in its sequence. We observed that decreased expression mainly affected the FBXW7β isoform and to a lesser extent FBXW7α and may be attributed to the combined effect of epigenetic changes, alteration of upstream factors and upregulation of miRNAs. Transient transfections with miRNA mimics in selected cell lines resulted in a significant decrease of total FBXW7 expression and its different isoforms separately, with the consequent increment of critical substrates and the stimulation of cell proliferation. Transient inhibition of endogenous miRNAs in a T-cell lymphoblastic-derived cell line (SUP-T1) was capable of reversing these proliferative effects. Finally, we show how FBXW7 isoforms display different roles within the cell. Simultaneous downregulation of the α and γ isoforms modulates the amount of CCNE1, whilst the β-isoform alone was found to have a prominent role in modulating the amount of c-MYC. Our data also revealed that downregulation of all isoforms is a sine qua non condition to induce a proliferative pattern in our cell model system. Taking these data into account, potential new treatments to reverse downregulation of all or a specific FBXW7 isoform may be an effective strategy to counteract the proliferative capacity of these tumour cells.
Publisher version (URL)http://dx.doi.org/10.1038/s41388-019-0746-1
URIhttp://hdl.handle.net/10261/219358
Identifiersdoi: 10.1038/s41388-019-0746-1
issn: 1476-5594
Appears in Collections:(CBM) Artículos
Files in This Item:
File Description SizeFormat 
Fernández-PiquerasJ_DownregulationofSpecificFBXW7.pdf5,2 MBAdobe PDFThumbnail
View/Open
Show full item record
Review this work
 

Related articles:


WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.