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

Targeted Re-engineering of the Tumor Matrix to Advance Immunotherapy

Project description

Rearranging the tumour matrix for enhanced immunotherapy

Tumour cells are surrounded and supported by an underlying connective tissue known as fibrotic stroma. This stroma comprises various components, including cancer-associated fibroblasts (CAFs) that produce extracellular matrix (ECM), influencing tumour biology, behaviour and response to therapy. The ERC-funded OpenMatrix project aims to address the negative impact of fibrotic stroma on immune cell recruitment and activation. The research team will identify and target this stroma-driving loop to normalise the perturbed ECM and enhance tumour accessibility for immune cells. By delineating CAF-ECM interactions, it will be possible to train tumour myeloid cells to alter the tumour ECM, reactivate the immune function and improve immunotherapy outcomes.

Objective

Immunotherapy can prolong lives of cancer patient subgroups, but fails in solid tumors with dense fibrotic stroma, such as pancreatic cancer. Fibrotic stroma prevents the recruitment and activation of immune effector cells, and, thereby dampens the efficacy of immunotherapy. Mechanistically, cancer-associated fibroblasts (CAFs) initiate extracellular matrix (ECM) production, which aggravates fibrosis by reciprocal mechanoactivation and crosstalk with tumor-associated myeloid cells, forming a self-sustainable “pro-fibrotic loop”. However, the central pathways initiating this vicious cycle and signaling compensation maintaining fibrosis under therapeutic conditions remain unclear. Consequently, clinical solutions to disrupt this pro-fibrotic loop are lacking.

I hypothesize that identifying and targeting the multi-step pro-fibrotic loop can be exploited to re-engineer and normalize the perturbed ECM and increase tumor accessibility for immune effector cells and immunotherapy.

To disrupt the pro-fibrotic loop, I will exploit an engineered modular peptido-/nanobio-mimetic toolbox, comprising nature-inspired targeting systems based on in silico design and experimental validation. The peptidomimetics and nano-biomimetics will target cellular interaction mechanisms to (1) inhibit CAF–ECM interactions driving tissue stiffening and fibrosis, and (2) train tumor myeloid cells towards matrix-degrading effectors to restructure fibrotic ECM. These biomimetics will be examined in advanced 3D in vitro and in vivo pancreatic tumor models. The combined effects of biomimetics on the matrisome, matrix architecture and single-cell transcriptomics will be integrated using machine learning to identify ECM fingerprints. OpenMatrix will 1) deliver mechanistic insights into endogenous fibrosis drivers and antagonists, 2) engage these cell-intrinsic mechanisms to revert fibrosis and, thereby, 3) reactivate immune effector function and advance immunotherapy.

Fields of science (EuroSciVoc)

CORDIS classifies projects with EuroSciVoc, a multilingual taxonomy of fields of science, through a semi-automatic process based on NLP techniques. See: The European Science Vocabulary.

You need to log in or register to use this function

Keywords

Project’s keywords as indicated by the project coordinator. Not to be confused with the EuroSciVoc taxonomy (Fields of science)

Programme(s)

Multi-annual funding programmes that define the EU’s priorities for research and innovation.

Topic(s)

Calls for proposals are divided into topics. A topic defines a specific subject or area for which applicants can submit proposals. The description of a topic comprises its specific scope and the expected impact of the funded project.

Funding Scheme

Funding scheme (or “Type of Action”) inside a programme with common features. It specifies: the scope of what is funded; the reimbursement rate; specific evaluation criteria to qualify for funding; and the use of simplified forms of costs like lump sums.

HORIZON-ERC - HORIZON ERC Grants

See all projects funded under this funding scheme

Call for proposal

Procedure for inviting applicants to submit project proposals, with the aim of receiving EU funding.

(opens in new window) ERC-2023-ADG

See all projects funded under this call

Host institution

UNIVERSITEIT TWENTE
Net EU contribution

Net EU financial contribution. The sum of money that the participant receives, deducted by the EU contribution to its linked third party. It considers the distribution of the EU financial contribution between direct beneficiaries of the project and other types of participants, like third-party participants.

€ 2 231 250,00
Address
DRIENERLOLAAN 5
7522 NB Enschede
Netherlands

See on map

Region
Oost-Nederland Overijssel Twente
Activity type
Higher or Secondary Education Establishments
Links
Total cost

The total costs incurred by this organisation to participate in the project, including direct and indirect costs. This amount is a subset of the overall project budget.

€ 2 231 250,00

Beneficiaries (2)

My booklet 0 0