NECESSITY · New prECision thErapieS for uveal melanoma (targeting the Gαq/GNAQ oncogenic Signaling cIrcuiTrY)
Horizon 2020 — Marie Skłodowska-Curie Actions
- Duration
- 2022-01-01 → 2024-12-31
- EU contribution
- €269,003
- Participants
- 2
- Scheme
- MSCA-IF
Lines connect the coordinator with its partners.
Results in brief
New prECision thErapieS for uveal melanoma (targeting the Gαq/GNAQ oncogenic Signaling cIrcuiTrY)
Uveal melanoma, the most common primary eye cancer in adults, has a high risk of metastasis to the liver within 5-10 years after diagnosis. Large tumors or relapses increase this risk. Despite dormancy in the liver after primary tumor treatment, once active, metastatic uveal melanoma is resistant to current therapies, resulting in rapid patient death within a year. Current treatments are ineffective, highlighting an urgent need for new strategies to address the significant threat of metastatic uveal melanoma and develop therapies for those facing a short life expectancy. Our studies have identified a promising approach to overcoming drug resistance in metastatic uveal melanoma. Specifically, we discovered that venetoclax, an approved BCL2 inhibitor, works synergistically with FAK/MEK blockade to restore treatment effectiveness. This suggests that resistance to FAK/MEK inhibitors in uveal melanoma cells may result from an adaptive increase in Bcl2, an anti-apoptotic protein. Targeting this pathway with BCL2 inhibitors could significantly enhance therapeutic responses, offering a more effective treatment strategy for patients facing limited options
Data: CORDIS, © European Union
Project objective
G protein-coupled receptors (GPCRs) represent the largest family of cell surface proteins involved in signal transmission. Nearly 30% of human cancers harbor mutations in GPCRs/G proteins. Activating mutations in GNAQ and GNA11 have been discovered in 90% of Uveal Melanoma (UM).UM is the most common primary cancer of the eye in adults and to date there are no effective treatments. 50% of UM patients develop metastatic disease, which is refractory to current chemotherapies leading to patient death within a year. Prolonged Gaq signaling leads to the activation of YAP, a transcriptional co-activator regulated, necessary for UM growth. GNAQ stimulates YAP through FAK. Inhibition of FAK reduces UM growth,leading FAK to be a potential therapeutic target for UM. In UM, the particular Gαq–regulated pathways that when overactive can render FAK inhibitor(FAKi) ineffective, as well as what feedback mechanisms should be targeted to optimize therapeutic responses to FAKi are still unknown. I will use a panel of GNAQ-driven UM cells and perform a genetic screen using the Cancer Signaling Toolkit to discover molecular determinants of sensitivity or resistance to FAK inhibition. Signaling candidates and screening hits discovered will be prioritized and their biological impact in UM growth and FAKi sensitivity will be evaluated. To increase FAKi activity and reduce therapy resistance, I will also investigate whether co-targeting candidate GNAQ-effector and FAKi resistance pathways will synergize with FAKi, resulting in UM cell death. Finally,I will explore the mechanism of UM cell death by co-targeting. My studies will reveal new targeted(precision) strategies for multiple Gαq-driven pathological conditions in cancer The project will be supervised by Dr. Gutikind and Dr.Martini two experts in GPRC/G proteins. Through this work, I aim to broaden my scientific expertise (including technical and transferable skills) and to establish myself as an independent researcher in cancer biology
Original text from CORDIS.
Participants
- UNIVERSITA DI PISA · PisaCoordinatorItaly
- THE REGENTS OF THE UNIVERSITY OF CALIFORNIA · OaklandUnited States
Links
Data: CORDIS, © European Union