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HOLDING-HANDS SIGNED

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

Total Cost €

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EC-Contrib. €

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Partnership

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 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.

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

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.
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 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

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