Research

Projects

Our vision is to create a smart digital pathology scanner that builds patient-specific tumour digital twins and simulates drug treatments. Using pancreatic cancer models, the project will integrate multi-omics, clinical data, AI and hardware design to help doctors personalize therapy.
SeleCStem aims to target the cancer stem cells responsible for therapy resistance and relapse. It will harness ALDH activity to deliver drugs selectively and inhibit tumours using light.
This project aims to transfer new guidelines for appropriate stone pine management, including the use of semiochemicals for the management of Leptoglossus occidentalis.
2G_PROVEIL aims to develop, scale up and commercialise a new generation of PROVEIL masks, based on a virucidal nanofibre technology, reaching the PPF3 level and incorporating a sensor to inform the user about the correct fit.
BubblyBots4BC develops a novel bladder cancer immunotherapy based on enzyme-powered iron oxide nanobots capable of accumulating in tumor tissue and generating laser-induced vapor nanobubbles. These nanobubbles seek to induce immunogenic cell death and promote in situ vaccination that stimulates antitumor immune responses.
We propose an innovative strategy based on photopharmacology to address various therapeutic needs, including cardiovascular diseases. This approach would enable precise and reversible regulation of cardiac activity, with potential to temporarily improve its function and help stabilize rhythm disturbances in critical situations.
This project investigates how the CERT protein contributes to chemotherapy resistance in aggressive breast cancer, including interactions with cancer-associated fibroblasts (CAFs), and explores whether reducing CERT can improve the response to treatment. To achieve this, the researchers have developed new PROTAC-based molecules that directly degrade CERT via the proteasome, with the aim of enhancing cancer cell death and validating CERT as a therapeutic target.
Proteins are modified through the covalent attachment of a wide variety of lipids, and these modifications regulate their localisation, interactions and function. This project aims to identify and quantify protein-bound lipids and generate modified proteins using chemical synthesis or semisynthesis methods.
This project studies the use of atmospheric non-thermal plasmas as a sustainable seed treatment to improve germination and initial growth under drought conditions. The work focuses on Mediterranean crops of agronomic and social interest, such as cereals, tomatoes, and alfalfa, in collaboration with partners from Spain, Tunisia, and Mauritania.
We are developing autophagy inhibitors that are activated by external light to selectively eliminate cancer stem cells. We follow two approaches based on photoswitches and photocages.
The DEEPPEST project develops a faster and more economical way to find naturally occurring chemical compounds to control insect pests, without having to resort to conventional pesticides, by combining artificial intelligence and computational chemistry with insect biology. The approach is tested on the Moroccan locust as a proof of concept that could subsequently be applied to other invasive species.
Current treatments for chronic and acute pain, such as opioids, act systemically and often cause severe side effects. Within the framework of this project, we are exploring the use of light-activatable drugs to achieve more precise, localized, and safer pain control.
The project seeks to generate robust environmental evidence for antimicrobial polymeric materials based on biodegradable cationic amphiphiles as a sustainable alternative to QACs. Functionalized PLA polymers and zein nanoparticles will be evaluated through standardized biodegradability and ecotoxicity assays.
Rare diseases present major therapeutic challenges and Myotonic Dystrophy remains without effective treatment due to its genetic complexity and the low efficacy of antisense oligonucleotides (ASO) tested. ENTRY DM trains 14 doctoral candidates in ASO, advanced models, and clinical preparation, strengthening European leadership and accelerating future trials.
The project studies how alternative translation initiation (ATI) can generate protein diversity without genetic changes, challenging the classical view of the Central Dogma of Biology. It proposes that ATI acts as a driver of molecular innovation and seeks to understand its mechanisms, its role in evolution, and its applications in synthetic biology.