Opendata, web and dolomites


The role of extra centrosomes on the tumour microenvironment

Total Cost €


EC-Contrib. €






Project "CentrosoTME" data sheet

The following table provides information about the project.


Organization address
address: 327 MILE END ROAD
city: LONDON
postcode: E1 4NS

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 United Kingdom [UK]
 Total cost 212˙933 €
 EC max contribution 212˙933 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2018
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2019
 Duration (year-month-day) from 2019-06-01   to  2021-05-31


Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    QUEEN MARY UNIVERSITY OF LONDON UK (LONDON) coordinator 212˙933.00


 Project objective

The centrosome, an organelle important for cell division, is frequently amplified in cancer, including breast cancer. In this fellowship I propose to investigate how cells with centrosome amplification change the tumour microenvironment (TME) to promote breast cancer development. Recent work has shown that having extra centrosomes drive tumour growth in vivo, indicating that centrosome amplification is not a bystander of cancer, but promotes tumorigenesis. Consistent with a direct role in cancer, we previously demonstrated that centrosome amplification leads to chromosome instability and cell invasion. In addition to the cell autonomous effects of centrosome amplification, our lab has recently found that cells containing extra centrosomes also have non-cell autonomous effects via secretion of proteins that induce a paracrine invasive phenotype in mammary organoids. We also found that cells with pancreatic cancer cells with extra centrosomes secrete small extracellular vesicles (sEVs) that induce activation of the fibroblast-like pancreatic stellate cells (PSCs). Moreover, using xenograft immunocompetent mouse models, we found that induction of centrosome amplification in SUM225 human breast cancer cells leads to a strong innate immune infiltration (e.g. macrophages and neutrophils) surrounding the tumours. Guided by our preliminary data we hypothesise that altered secretion in cells with centrosome amplification changes the TME. Currently there is no published link between centrosome amplification and TME. I aim to characterise TME changes induced by centrosome amplification in vivo and to identify factors secreted by cells with extra centrosomes responsible for such changes. This work will be the first in-depth characterisation of TME in tumours containing extra centrosomes. Importantly, this project will start an exciting and novel research avenue bridging the centrosome and the TME fields.

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "CENTROSOTME" project.

For instance: the website url (it has not provided by EU-opendata yet), the logo, a more detailed description of the project (in plain text as a rtf file or a word file), some pictures (as picture files, not embedded into any word file), twitter account, linkedin page, etc.

Send me an  email ( and I put them in your project's page as son as possible.

Thanks. And then put a link of this page into your project's website.

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

More projects from the same programme (H2020-EU.1.3.2.)

SIMIS (2020)

Strongly Interacting Mass Imbalanced Superfluid with ultracold fermions

Read More  

COLEX (2019)

Coopetition and Legislation in the Spanish Netherlands (1598-1665)

Read More  

NPsVLCD (2019)

Natural Product-Inspired Therapies for Leishmaniasis and Chagas Disease

Read More