#	Pagina
attuale pagina	/open-h2020/projects/210074/index.html

Opendata, web and dolomites

META-DORM SIGNED

Mechanobiology of METAstatic and DORMant cancer cells in bone marrow lesions

Total Cost €

EC-Contrib. €

Partnership

Views

Outcomes and
results

META-DORM project word cloud

Explore the words cloud of the META-DORM project. It provides you a very rough idea of what is the project "META-DORM" about.

stimulation bone chemical niche mechanisms resorption cancer warning primary chemosensing prevention mechanosensor prevent tumour cells explore time mechanical skeletal implicated resistant chemotherapy mechanobiological significantly homeostatic metastatic cell hijacking environment active remodelling therapeutic cycle normal while quiescent shed culturing remission interactions rates months sites usually light marrow poorly first will intriguingly plays form treatment cellular physical metastasis reactivate tumours observe fatal cilium dormant decreases dormancy once types persist roles signalling reside effect invaded lesions survival dramatically balance individual radiation mechanically suggests

Project "META-DORM" data sheet

The following table provides information about the project.

Coordinator	QUEEN MARY UNIVERSITY OF LONDON Organization address address: 327 MILE END ROAD city: LONDON postcode: E1 4NS website: http://www.qmul.ac.uk 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]
Project website	https://stefaanverbruggen.com/
Total cost	183˙792 €
EC max contribution	183˙792 € (100%)
Programme	1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
Code Call	H2020-MSCA-IF-2016
Funding Scheme	MSCA-IF-GF
Starting year	2018
Duration (year-month-day)	from 2018-01-01 to 2020-06-29

Partnership

Take a look of project's partnership.

#	participants	country	role	EC contrib. [€]
1	QUEEN MARY UNIVERSITY OF LONDON QUEEN MARY UNIVERSITY OF LONDON Organization address address: 327 MILE END ROAD city: LONDON postcode: E1 4NS website: http://www.qmul.ac.uk contact info title: n.a. name: n.a. surname: n.a. function: n.a. email: n.a. telephone: n.a. fax: n.a.	UK (LONDON)	coordinator	183˙792.00
2	TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK Organization address address: AMSTERDAM AVENUE 1210 ROOM city: NEW YORK postcode: 10027 7003 website: www.columbia.edu contact info title: n.a. name: n.a. surname: n.a. function: n.a. email: n.a. telephone: n.a. fax: n.a.	US (NEW YORK)	partner	0.00

Map

Project objective

While cancer survival rates have improved significantly in recent years, survival decreases dramatically after tumour metastasis. One of the most common sites for metastatic tumours to develop is bone. Intriguingly, evidence suggests that once they have invaded the bone marrow, individual metastatic cancer cells can persist for years in a quiescent or “dormant” state, and are resistant to both radiation and chemotherapy treatment. These dormant cells can reside for months or years while the cancer is in remission, and then “reactivate” without warning to form new, usually fatal, skeletal lesions. Tumour cells achieve this by “hijacking” the normal bone remodelling cycle, a homeostatic balance between bone formation and resorption, to form a metastatic niche within the marrow. However, the signalling mechanisms that cause metastasis and dormancy, particularly in such a mechanically active environment, are poorly understood. Therefore, the goal of this project is to investigate the chemical and physical interactions between bone and cancer cells, both during dormancy and mechanical stimulation, to provide new insight into bone metastatic lesions and explore novel therapeutic targets to prevent cancer metastasis. This will be achieved by culturing specific bone and cancer cell types together for the first time to observe changes in their signalling and behaviour. Dormancy will also be induced, to observe its effect on changes in signalling. Mechanical stimulation will be applied to investigate whether the complex mechanical environment of the bone marrow plays a role in cancer metastasis. Finally, a specific cellular mechanosensor, the primary cilium, which has been implicated in the development of cancer and is known to be involved in bone formation, will be investigated. This will shed new light on its chemosensing and mechanobiological roles in cancer metastasis, as well as explore its potential as a novel target for cancer treatment and prevention.

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "META-DORM" 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 (fabio@fabiodisconzi.com) 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 "META-DORM" are provided by the European Opendata Portal: CORDIS opendata.