Skip to main content
Go to the home page of the European Commission (opens in new window)
English en
CORDIS - EU research results
CORDIS

Deciphering the COMPASS that guides cancer

Project description

Targeting cancer through epigenetics

New therapies for cancer depend on understanding the genes that control cell behaviour. However, many mechanisms remain hidden. Mutations in KMT2D, KMT2C and KDM6A – key members of the COMPASS-like complex – are frequent in cancers and aged epithelial cells, affecting differentiation, tissue homeostasis and tumour progression. With this in mind, the ERC-funded COMPASS project will use single-cell lineage tracing, genomics, epigenomics, CRISPR-based gene editing and pharmacologic interventions to study how these mutations influence cell states, tumour initiation, heterogeneity and metastasis in skin and bladder cancers. Genome-wide CRISPR screens will identify synthetic lethal genes, revealing new vulnerabilities in cancer cells. The project’s goal is to guide the development of targeted therapies and deepen our understanding of tumour biology.

Objective

Epigenetic features are commonly dysregulated in cancer and one of the surprising findings from the sequencing of cancer genomes is the high rate of alterations in many epigenetic regulators. KMT2D/MLL4, KMT2C/MLL3 and KDM6A/UTX are among the most frequently mutated genes in a wide range of cancers and in normal aged epithelial cells. Interestingly, these three genes are components of the same complex, COMPASS-like complex that regulate enhancer activity and regulate gene expression in a lineage specific manner. The deletion of members of the COMPASS-like complex has been associated with altered differentiation, aging and tumorigenesis. However, the precise mechanisms by which mutations in these genes impact cell states during tissue homeostasis, tumour initiation, tumour heterogeneity and metastasis, remain poorly understood. To address these important questions, we will use multidisciplinary approaches that will combine in vivo single cell lineage tracing, single-cell genomics, epigenomics and transcriptomics, in vivo CRISPR-based gene editing, together with genetic and pharmacologic perturbations, to define in a comprehensive and integrated manner the impact of Kmt2d, Kmt2c and Kdm6a deletion on cell state dynamics during homeostasis, regeneration, early steps of tumour initiation, tumour heterogeneity and metastasis in skin squamous cell carcinoma and bladder cancer. Moreover, we will perform genome wide CRISPR-Cas9 screen to identify the synthetically lethal genes in KMT2D, KMT2C and KDM6A mutated cancer cells to uncover new tumour vulnerabilities that can be pharmacologically targeted.

Fields of science (EuroSciVoc)

Keywords

Programme(s)

Topic(s)

Funding Scheme

HORIZON-ERC - HORIZON ERC Grants

See all projects funded under this funding scheme

Call for proposal

(opens in new window) ERC-2025-STG

See all projects funded under this call

Host institution

UNIVERSITE LIBRE DE BRUXELLES
Net EU contribution
€ 2 000 000,00
Address
AVENUE FRANKLIN ROOSEVELT 50
1050 BRUXELLES
Belgium
Region
Région de Bruxelles-Capitale/Brussels Hoofdstedelijk Gewest Région de Bruxelles-Capitale/ Brussels Hoofdstedelijk Gewest Arr. de Bruxelles-Capitale/Arr. Brussel-Hoofdstad
Activity type
Higher or Secondary Education Establishments
Links
Total cost
€ 2 000 000,00

Beneficiaries (1)