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SyLeNCe SIGNED

Synapses between Leukaemia and its Neighbouring Cells

Total Cost €

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EC-Contrib. €

0

Partnership

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 SyLeNCe project word cloud

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

tumor    our    hope    tissue    tri    sequencing    stem    appreciate    transformation    validate    progression    dimensional    relationships    interdisciplinary    biology    gathered    elegant    time    models    candidates    candidate    landscape    comprise    unravel    map    rna    niches    tissues    look    lineage    mouse    acute    vulnerabilities    input    complexity    assays    single    neoplastic    primary    complete    vitro    quality    stroma    transcriptional    description    constitute    life    homeostasis    survival    vivo    dissecting    experiments    myeloid    function    list    murine    layers    flow    treatment    cells    ecosystem    genetic    niche    perhaps    parametric    first    leukemia    organization    revealing    reductionist    intervention    fails    populations    microenvironment    therapeutically    heterotypic    gain    limited    samples    environment    cytometry    explored    tightly    human    unidirectional    exist    recognize    sylence    start    leukaemia    molecular    share    proven    nature    question    aml    bone    marrow    patients    disease    cellular    completion    cell    efficient    interactions    opportunity    fashion    therapeutic    hence   

Project "SyLeNCe" data sheet

The following table provides information about the project.

Coordinator
FUNDACION PARA LA INVESTIGACION MEDICA APLICADA FIMA 

Organization address
address: AVENIDA DE PIO XII 55
city: PAMPLONA
postcode: 31008
website: www.cima.es

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 Spain [ES]
 Total cost 160˙932 €
 EC max contribution 160˙932 € (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-RI
 Starting year 2020
 Duration (year-month-day) from 2020-07-01   to  2022-06-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    FUNDACION PARA LA INVESTIGACION MEDICA APLICADA FIMA ES (PAMPLONA) coordinator 160˙932.00

Map

 Project objective

Our understanding of the different layers of organization in tissues remains limited. Stem cell niches offer a tightly controlled environment and a unique opportunity to look into this question. Reductionist approaches have been proven highly efficient dissecting the complexity of stem cell niches in a unidirectional fashion. However, this approach fails to recognize the tri-dimensional complexity of tissue organization. Hence we propose a systems biology approach based on low input and single cell RNA sequencing of bone marrow niche populations in order to establish not only the molecular landscape of cells that comprise the stem cell niche in homeostasis and disease but also the lineage relationships that may exist between cells in the stroma. Using the mouse bone marrow niche during neoplastic transformation to acute myeloid leukemia (AML), we will first unravel the cellular and molecular interactions that constitute the tumor microenvironment during disease development and progression using multi parametric flow cytometry and RNA-sequencing. Information gathered from these experiments will also provide a list of molecular candidates for therapeutic intervention in AML. We will validate those candidate cell populations and genetic pathways by means of gain and loss-of-function assays in vitro and in vivo using murine models and primary human AML samples. Completion of our interdisciplinary project will provide, for the first time a complete transcriptional and cellular map of a tissue, revealing the heterotypic interactions that define the real nature of a tissue. Perhaps then we could start to appreciate the elegant complexity of the ecosystem that the stem cell and its niche share. I hope SyLeNCe will facilitate the description of novel vulnerabilities that could be explored therapeutically for the treatment of acute myeloid leukaemia having an impact on the quality of life and long-term survival of AML patients.

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

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