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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.

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

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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