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Tissue-engineering the tumour microenvironment to improve treatment of pancreatic cancer

Project description

Patient-derived in vitro models of pancreatic cancer

Pancreatic cancer is associated with an extremely poor prognosis, necessitating the development of novel therapies. This requires patient-specific models that mimic the biology of the tumour and the interaction between cancer and cancer-supporting cells. To address this issue, the EU-funded CHIPIN project proposes to develop 3D cancer models using tissue engineering and bioprinting. The built platforms will consist of hydrogels, extracellular matrix molecules and patient-derived cells and will recreate the biomechanical characteristics of the pancreatic tumour microenvironment. This new approach will offer a clinically relevant platform for screening novel therapies.

Objective

My vision is to address a clinical problem with a novel and transformative approach. Using my unique expertise in cell biology, tissue engineering and translational research I will design technology platforms to test new treatments for human pancreatic cancer.

Pancreatic tumours are cancers of unmet medical need with 85% of patients dying within 9 months of diagnosis. To find better therapies, we need patient-specific models that mimic the biology of tumour tissues and target interactions between malignant and non-malignant cells. Biomimetic tissue engineering is a powerful approach to generate 3D cancer models, however, only a few scientists use these technologies. Most 3D cultures of human cells include reconstituted matrices that originate from murine tumours containing undefined amounts of extracellular matrix and growth factors. There is no tissue-engineered 3D model that allows control over patient-specific and biomechanical characteristics of the pancreatic tumour microenvironment.

I hypothesise that 3D approaches that replicate the native tissue composition and biomechanical properties will behave like real tumours to provide clinically predictive platforms and to test novel treatments that target both malignant and non-malignant cells.

To test my hypothesis, I will:
•3D-print matrix and cellular elements of the microenvironment of human pancreatic tumours
•Develop a cancer-on-a-chip model of liver metastasis
•Compare the crosstalk of malignant and other microenvironment components with the human disease
•Validate my new platforms with treatments in clinical trials and test novel combination treatments that slow down or reduce tumour growth.

In a multidisciplinary project, I will use:
•3D printing to build platforms composed of hydrogels, fibrous scaffolds and patient-derived cells
•Extracellular matrix molecules for chemical crosslinking into hydrogels
•Cancer-on-a-chip models to study tumour metastasis
•Imaging, biomechanical and multi-omics analyses.

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Keywords

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Programme(s)

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Topic(s)

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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.

ERC-COG - Consolidator Grant

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Call for proposal

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

(opens in new window) ERC-2019-COG

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Host institution

LEIBNIZ-INSTITUT FUR POLYMERFORSCHUNG DRESDEN EV
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.

€ 2 000 000,00
Address
HOHE STRASSE 6
01069 Dresden
Germany

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Region
Sachsen Dresden Dresden, Kreisfreie Stadt
Activity type
Research Organisations
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.

€ 2 000 000,00

Beneficiaries (1)

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