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Exploiting the activity of the ALDH enzyme to develop highly selective drugs for cancer stem cells

Descrizione del progetto

Un approccio innovativo per intervenire sulle cellule staminali del cancro

Prove sempre più numerose rafforzano la teoria secondo cui il cancro viene sviluppato e mantenuto da una sottopopolazione di cellule tumorali con le proprietà delle cellule staminali. Queste cellule staminali tumorali (CSC) in genere si trovano in uno stato di quiescenza, che le rende resistenti alle terapie standard e responsabili della ricaduta della malattia. Il progetto SeleCStem, finanziato dal CER, si propone di sviluppare strategie innovative per colpire efficacemente le CSC sfruttando l’enzima aldeide deidrogenasi (ALDH), che è sovraespresso nelle CSC in vari tipi di cancro. Il team di ricerca sfrutterà l’attività dell’enzima per rilasciare selettivamente i farmaci nelle CSC e la combinerà con l’inibizione dell’ALDH mediata dalla luce nei tumori.

Obiettivo

Despite huge advances in cancer treatment, resistance to chemotherapy is still common. It is now well established that a small population of cells named cancer stem cells (CSCs) have high tumorigenicity and are able to initiate and maintain a tumour. CSCs usually remain in a quiescent state that is not affected by standard chemotherapy; thus, they are often responsible for treatment resistance and relapse. There is a clear need to find effective treatments against CSCs to fully eradicate the tumour. However, the close similarities of CSCs to healthy stem cells hinders the identification of selective drugs.
In the last years, new drug modalities are emerging to provide therapeutic options for challenging targets and diseases, expanding the drug discovery landscape. In line with these trends, SeleCStem aims to develop innovative chemical biology strategies to target CSCs in a safe and effective manner. It will exploit the activity of the enzyme ALDH, which is overexpressed in CSCs of many cancer types, to obtain selective drugs using three orthogonal strategies: we will use the oxidoreductase activity of ALDH to trigger the selective (1) accumulation or (2) release of drugs inside CSCs and (3) use external light to inhibit ALDH only in the tumour area. Successful strategies will be combined at the end of the project to overcome potential limitations of the individual approaches, hence massively increasing the drugs’ selectivity and efficacy. We will design these molecules with the aid of docking studies, synthesise them, and assess their ALDH- or light-triggered activation in purified enzyme assays and in CSC spheres.
Overall, we will develop the proof of concept of unprecedented approaches to eliminate CSCs with outstanding precision, thus overcoming some of the limitations of conventional small molecules going beyond state-of-the-art chemical biology. Our ultimate goal is to contribute to improve cancer treatment and increase complete remission rates.

Campo scientifico (EuroSciVoc)

Parole chiave

Programma(i)

Argomento(i)

Meccanismo di finanziamento

HORIZON-ERC - HORIZON ERC Grants

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(si apre in una nuova finestra) ERC-2024-STG

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Istituzione ospitante

AGENCIA ESTATAL CONSEJO SUPERIOR DE INVESTIGACIONES CIENTIFICAS
Contributo netto dell'UE
€ 1 499 948,00
Indirizzo
CALLE SERRANO 117
28006 Madrid
Spagna
Regione
Comunidad de Madrid Comunidad de Madrid Madrid
Tipo di attività
Research Organisations
Collegamenti
Costo totale
€ 1 499 948,00

Beneficiari (1)