Descrizione del progetto
Dissezione delle caratteristiche del cancro per il trattamento
La transizione epiteliale-mesenchimale (EMT, Epithelial-to-Mesenchymal Transition) è un processo in base al quale le cellule epiteliali vengono trasformate in cellule mesenchimali, acquisendo la capacità di staccarsi dal tessuto originale e migrare verso altri siti. Oltre al normale sviluppo, l’EMT è attiva anche nel cancro dove guida la dissociazione e la metastasi delle cellule tumorali, oltre a dotare le cellule tumorali di proprietà delle cellule staminali e resistenza ai farmaci. Il progetto NetriCan, finanziato dall’UE, studierà in quale modo una proteina extracellulare, nota per il suo ruolo nella migrazione cellulare durante lo sviluppo, regola l’EMT nelle cellule tumorali. I risultati del progetto confermeranno il potenziale terapeutico di una strategia volta a colpire questa proteina e aiuteranno a sviluppare nuovi approcci terapeutici promettenti per i pazienti con tumori solidi avanzati.
Obiettivo
Recent data coming from both basic research and clinical trials converge toward the importance of the epithelial/mesenchymal status of a tumor to respond to conventional chemotherapies and immune-checkpoint inhibitors. These observations set the Epithelial-to-Mesenchymal Transition (EMT) program at the centre of cancer biology. Besides its multiple roles in development and during adulthood, EMT is activated during tumor progression not only to allow metastatic dissemination of cancer cells, which is responsible for the vast majority of patients’ death, but also to provide cells with stem-like properties and resistance mechanisms to survive chemotherapy. It is now widely accepted that future therapies will have to target and/or block the EMT process and allow conventional therapies to efficiently kill the differentiated, epithelial cells to treat patients with advanced solid tumors. NetriCan will analyse for the first time the implication of netrin-1 and its dependence receptor UNC5B in the regulation of EMT, either directly or via its cell death-related function. Moreover, the re-epithelialization effect of the anti-netrin-1 monoclonal antibody observed in tumors in vivo and in a preliminary cohort of patients shows that netrin-1/UNC5B may not only be involved in the direct regulation of maintenance of EMT but also serve as a survival mechanism for metastatic tumor cells. To achieve this, Netrican will first analyse how the upregulation of netrin-1 and UNC5B is regulated during EMT. It will then investigate the role of the netrin-1/UNC5B axis in the establishment and maintenance of the EMT program needed for cell dissemination and metastasis. Finally, this project will elucidate the therapeutic potential of the anti-netrin-1 strategy for both triggering primary tumor re-epithelialization and killing mesenchymal tumor cells. In summary, NetriCan will provide innovative findings to develop novel promising therapeutic approach for patients with advanced solid tumors.
Campo scientifico
Programma(i)
Argomento(i)
Meccanismo di finanziamento
MSCA-IF - Marie Skłodowska-Curie Individual Fellowships (IF)Coordinatore
69622 Villeurbanne Cedex
Francia