Projektbeschreibung
Analyse von Krebsmerkmalen für die Behandlung
Die epithelial-mesenchymale Transition (EMT) ist ein Vorgang, bei dem Epithelzellen in Mesenchymzellen umgewandelt werden, um sich vom Ursprungsgewebe zu lösen und andere Stellen zu besiedeln. Neben der normalen Entwicklung ist die epithelial-mesenchymale Transition bei der den Krebs vorantreibenden Dissoziation von Tumorzellen aktiv und fördert die Metastasierung von Tumorzellen. Außerdem verleiht sie Krebszellen Stammzelleigenschaften sowie Arzneimittelresistenz. Das EU-finanzierte Projekt NetriCan wird untersuchen, wie ein extrazelluläres Protein, das für seine Rolle bei der Zellmigration während der Entwicklung bekannt ist, die epithelial-mesenchymale Transition in Krebszellen reguliert. Die Ergebnisse des Projekts werden das therapeutische Potenzial einer Strategie zur Bekämpfung dieses Proteins untermauern und zur Entwicklung von neuen, vielversprechenden Therapieansätzen für Betroffene mit fortgeschrittenen soliden Tumoren beitragen.
Ziel
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.
Wissenschaftliches Gebiet
Schlüsselbegriffe
Programm/Programme
Thema/Themen
Aufforderung zur Vorschlagseinreichung
Andere Projekte für diesen Aufruf anzeigenFinanzierungsplan
MSCA-IF - Marie Skłodowska-Curie Individual Fellowships (IF)Koordinator
69622 Villeurbanne Cedex
Frankreich