Opendata, web and dolomites

HOLDING-HANDS SIGNED

Holding hands: cell-cell junctions in breast cancer metastasis and resistance to therapy

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 HOLDING-HANDS project word cloud

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

off    worldwide    patient    deposits    cellular    breast    driving    2014    cldn3    samples    disease    science    mechanism    predominant    dsg2    site    metastatic    models    fundamental    tjp2    highlight    distant    symptoms    times    unexpectedly    options    clinical    unappreciated    previously    cells    vivo    basic    junction    occurs    mechanisms    migratory    types    sites    al    questions    unequivocally    therapies    cross    junctions    notion    therapy    metastases    break    preliminary    unprecedented    critical    components    lesion    incurable    die    dominated    cancer    goals    largely    prevent    blood    500000    therapeutic    patients    single    block    form    mouse    desmosome    tumor    suggest    first    targetable    signaling    cell    disseminate    metastasis    primarily    ing    involvement    tight    women    desmosomes    data    groupings    primary    spread    agents    actively    aceto    class    boundaries    et    shown    ambition    deaths   

Project "HOLDING-HANDS" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITAT BASEL 

Organization address
address: PETERSPLATZ 1
city: BASEL
postcode: 4051
website: www.unibas.ch

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 Switzerland [CH]
 Project website http://www.cancermetastasislab.com/
 Total cost 1˙744˙921 €
 EC max contribution 1˙744˙921 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2015-STG
 Funding Scheme ERC-STG
 Starting year 2016
 Duration (year-month-day) from 2016-03-01   to  2021-02-28

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITAT BASEL CH (BASEL) coordinator 1˙744˙921.00

Map

 Project objective

Breast cancer is the most common cancer in women, resulting in as many as 500000 deaths per year worldwide. Patients with breast cancer die unequivocally because of the development of incurable distant metastases and not because of symptoms related to the primary site. Understanding the complex, yet fundamental mechanisms driving breast cancer metastasis is critical to develop therapies tailored to this disease. The current understanding of how metastasis occurs is derived primarily from mouse models and largely dominated by the notion that single migratory cancer cells within the primary tumor can actively disseminate to distant sites and develop as metastatic deposits. Unexpectedly, our very recent study on patient blood samples has shown that cancer cell groupings, held together through strong cell-cell junctions, can break off the primary tumor and form a metastatic lesion up to 50 times more efficiently than single migratory cancer cells (Aceto et al, Cell, 2014). These findings lead to new open questions, yet highlight a previously unappreciated and targetable mechanism of cancer dissemination. Our preliminary data suggest that, among all types of cell-cell junctions, desmosomes and tight junctions are involved in this process, and therefore represent unprecedented options for developing a metastasis-tailored therapy for breast cancer. The two predominant goals of this proposal are: first, to define the role of specific desmosome (DSG2) and tight junction (CLDN3 and TJP2) components in the development of metastasis. Second, to address their involvement in cellular signaling and response to therapy. These studies will not only use our first-of-a-kind in vivo models developed from patients with breast cancer metastases, but also cross the boundaries between basic science and clinical applications. Our research has the long-term ambition to lead to a novel class of therapeutic agents tailored to block cell-cell junctions and prevent metastatic spread of cancer.

 Publications

year authors and title journal last update
List of publications.
2019 Gkountela S, Castro-Giner F, Szczerba BM, Vetter M, Landin J, Scherrer R, Krol I, Scheidmann MC, Beisel C, Stirnimann CU, Kurzeder C, Heinzelmann-Schwarz V, Rochlitz C, Weber WP, Aceto N.
Circulating Tumor Cell Clustering Shapes DNA Methylation to Enable Metastasis Seeding
published pages: , ISSN: 0092-8674, DOI:
Cell 2019-10-08
2019 Szczerba BM, Castro-Giner F, Vetter M, Krol I, Gkountela S, Landin J, Scheidmann MC, Donato C, Scherrer R, Singer J, Beisel C, Kurzeder C, Heinzelmann-Schwarz V, Rochlitz C, Weber WP, Beerenwinkel N, Aceto N.
Neutrophils escort circulating tumour cells to enable cell cycle progression
published pages: , ISSN: 0028-0836, DOI:
Nature 2019-10-08

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "HOLDING-HANDS" 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 "HOLDING-HANDS" are provided by the European Opendata Portal: CORDIS opendata.

More projects from the same programme (H2020-EU.1.1.)

KineTic (2020)

New Reagents for Quantifying the Routing and Kinetics of T-cell Activation

Read More  

TechChange (2019)

Technological Change: New Sources, Consequences, and Impact Mitigation

Read More  

CARBYNE (2020)

New carbon reactivity rules for molecular editing

Read More