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Flow and Deformation of Cancer tumours near Yielding

Total Cost €


EC-Contrib. €






Project "FanCY" data sheet

The following table provides information about the project.


Organization address
address: STEVINWEG 1
city: DELFT
postcode: 2628 CN

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Netherlands [NL]
 Total cost 2˙000˙000 €
 EC max contribution 2˙000˙000 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-COG
 Funding Scheme ERC-COG
 Starting year 2019
 Duration (year-month-day) from 2019-04-01   to  2024-03-31


Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    TECHNISCHE UNIVERSITEIT DELFT NL (DELFT) coordinator 2˙000˙000.00


 Project objective

The aim of this proposal is to understand when, how and why metastatic tumour cells detach from a tumour.

Often, primary tumours do not kill patients, but secondary tumours do. These so-called metastatic tumour cells disassociate from a primary tumour and, ultimately, prove fatal. Currently, we do not understand the fundamentals of the biophysical pathways and mechanisms of the metastasis of cancer, hampering medical intervention. I propose a multidisciplinary approach, combining engineering, chemistry, biophysics and cell biology to identify the mechanical pathways for the creation of metastatic cancer cells.

Biological cells in tissue are very densely packed, which locks them in place relative to their neighbours, a state referred to as jammed. The collective system of cells can become fluidised locally and flow when pushed or deformed. Even greater forces can make the entire tissue fluid-like, referred to as yielding. The crucial open questions are: how does tissue yield, and what universal physics underlies yielding?

I will develop a novel fundamental and predictive description of yielding in jammed living tissue to show: 1. How and when jammed living cells are driven to fluid-like state. 2. How confinement tunes the migration mode of cancer cells. 3. How yielding is related to the structural evolution of detached cells. 4. How critical scaling controls deformation and flow of living cells near yielding.

I will demonstrate that the distance to yielding governs the mechanical response in collective cell motion inside a tumour, and that exploiting critical scaling allows predicting the dynamics of cell detachment near yielding. The outcomes will significantly aid the treatment of cancer in the near future by bridging the gap between chemical and mechanical pathways of cancer metastasis. I have the required multidisciplinary track record. Moreover, preliminary experiments show highly promising results.

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The information about "FANCY" are provided by the European Opendata Portal: CORDIS opendata.

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