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MICRONEX SIGNED

Microbioreactor platforms as in vivo-like systems to probe the role of Neuroblastoma-derived Exosomes in cancer dissemination

Total Cost €

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EC-Contrib. €

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Partnership

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 MICRONEX project word cloud

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

laboratory    concentration    cancer    cure    limitation    language    fast    milieu    scenarios    limitations    malignant    unexplored    model    regulating    completely    microbioreactors    interactions    phenomena    discoveries    poorly    shedding    techniques    thought    experiments    conditioning    sciences    laws    env    tissues    engineers    tumors    difficulty    previously    culture    bodies    predicting    sound    tumor    parallelized    comfort    life    zones    physics    readouts    reconstructing    platforms    vitro    reconstruct    scientists    reside    biological    tools    standard    human    reshape    induce    function    prognosis    fate    felt    solid    leaders    progression    vivo    bridge    situation    edge    technologies    complexity    niches    multifactorial    neuroblastoma    gradients    exosomes    thermodynamics    pediatric    heterogeneous    brs    mathematics    engineering    organs    microenvironment    time    generate    principles    biologically    light    local    secreted    disease    actively    nb    space    difficult    ground    health    translate    distant    resolved    mu    lacking    performing    gap    cells    decoding    medical    hypothesize    dynamic    revolutionize    extremely    nbs    mechanisms    models   

Project "MICRONEX" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITA DEGLI STUDI DI PADOVA 

Organization address
address: VIA 8 FEBBRAIO 2
city: PADOVA
postcode: 35122
website: www.unipd.it

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 Italy [IT]
 Total cost 1˙446˙250 €
 EC max contribution 1˙446˙250 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2017-STG
 Funding Scheme ERC-STG
 Starting year 2017
 Duration (year-month-day) from 2017-12-01   to  2022-11-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITA DEGLI STUDI DI PADOVA IT (PADOVA) coordinator 1˙446˙250.00

Map

 Project objective

Engineers can actively contribute to fields thought to be out of their “comfort zones”. We can be leaders of discoveries that translate into advances in the understanding of disease and improving human health. Engineers might use different language and tools than Life Sciences Scientists but we find a common ground, as the laws of Thermodynamics, Physics, and Mathematics also apply to biological phenomena. The development of microbioreactors (μBRs) reconstructing biologically sound niches can revolutionize medical research. In our bodies cells reside in a complex milieu, the microenvironment (μEnv), regulating their fate and function. Most of this complexity is lacking in standard laboratory models, leading to readouts poorly predicting the in vivo situation. This is particularly felt in cancer research, as tumors are extremely heterogeneous and capable of conditioning both the local μEnv and distant organs. Neuroblastoma (NB) is the most common and difficult to cure pediatric malignant solid tumor. Secreted exosomes are means by which NBs reshape their μEnv and induce local and long-range changes in cells, regulating progression and prognosis. But the mechanisms involved are yet not completely understood. A major limitation is the difficulty to model in vitro the local in vivo dynamic μEnv. We hypothesize that μBRs exploiting classical engineering principles will solve the limitations of existing classical culture models. We propose to develop platforms and test their edge over classical approaches in decoding the role of exosomes and μEnv in NB. Our μBRs generate time and space-resolved concentration gradients, support fast dynamic changes and reconstruct complex interactions between cells and tissues while performing multifactorial and parallelized experiments. We expect that our technologies will bridge the gap between in vitro techniques and in vivo biological phenomena leading to significant and novel results, shedding light on previously unexplored scenarios.

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