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miRCaP SIGNED

Innovative nanoparticle formulation for a miR-133 based treatment of cardiac hypertrophy

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 miRCaP project word cloud

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

toxic    causes    population    identification    line    cardiac    contraction    players    candidates    outcome    found    capitalist    failing    pathological    heart    mir    strategic    microrna    50    worldwide    remarkable    individual    ca    therapeutic    functionalize    stress    nanoparticle    drug    generate    remodeling    cardiovascular    calcium    post    micrornas       paid    toxicity    phosphate    intellectual    attracted    innovative    formulation    venture    roles    preclinical    strategies    regulate    133    relies    hypertrophy    ing    genes    translation    inversely    proof    ischemic    biocompatible    levels    release    specificity    genetic    govern    germane    preventing    dysregulations    unveiled    structural    bioresorbable    efficient    np    strategy    multiple    etiologies    mir133    muscle    cell    business    treatment    defects    selective    inflammatory    diagnosis    nanoparticles    successful    diseases    mortality    cds    drugs    cap    efficiency    selectively    commercial    patient    pathogenesis    additional    nps    unexpected   

Project "miRCaP" data sheet

The following table provides information about the project.

Coordinator
HUMANITAS MIRASOLE SPA 

Organization address
address: VIA MANZONI 56
city: ROZZANO (MI)
postcode: 20100
website: www.humanitas.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 150˙000 €
 EC max contribution 150˙000 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2015-PoC
 Funding Scheme ERC-POC
 Starting year 2016
 Duration (year-month-day) from 2016-12-01   to  2018-05-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    HUMANITAS MIRASOLE SPA IT (ROZZANO (MI)) coordinator 150˙000.00

Map

 Project objective

Innovative nanoparticle formulation for a miR-133 based treatment of cardiac hypertrophy

Cardiovascular diseases (CDs) are growing problems worldwide, affecting as much as 1% of the population. The causes include ischemic, toxic, genetic, post-inflammatory and structural defects; often multiple etiologies are present within an individual patient germane to the contraction failing, resulting in a mortality of ca. 50% within 5 years from diagnosis. Unexpected roles have been unveiled for microRNAs, important key-players in such pathogenesis, able to regulate levels of genes that govern cell remodeling. In line with this, development of microRNA-based drugs aimed at preventing stress-induced dysregulations of microRNA levels has attracted remarkable attention as potential candidates for therapeutic applications. Particular attention is paid to the miR-133, a muscle-specific microRNA, which has been found inversely related to pathological cardiac hypertrophy. However, a key challenge of microRNA-based drugs relies on delivery efficiency, toxicity and specificity. Here, we propose to generate innovative and effective therapeutic strategies based on the development of novel biocompatible and bioresorbable calcium phosphate nanoparticles (CaP-NP) for carrying miR-133 selectively to the heart. Our aim is to functionalize CaP-NPs for a selective delivery of the therapeutic miR133 to the pathological heart. The development of a novel approach based on CaP-NPs might be an efficient cardiac drug-delivery system for a specific release of miR-133. The successful outcome of this proposal will provide a relevant preclinical proof-of-concept necessary for 1) the development of additional Intellectual Properties, 2) the translation into a commercial strategy and business case, and 3) the identification of strategic partners and venture capitalist.

 Publications

year authors and title journal last update
List of publications.
2018 Irene Salamon, Gloria Saccani Jotti, Gianluigi Condorelli
The long noncoding RNA landscape in cardiovascular disease
published pages: 1, ISSN: 0268-4705, DOI: 10.1097/HCO.0000000000000507
Current Opinion in Cardiology 2019-06-13
2018 Serge Masson, Sandor Batkai, Julia Beermann, Christian Bär, Angelika Pfanne, Sabrina Thum, Michela Magnoli, Giovanna Balconi, Gian Luigi Nicolosi, Luigi Tavazzi, Roberto Latini, Thomas Thum
Circulating microRNA-132 levels improve risk prediction for heart failure hospitalization in patients with chronic heart failure
published pages: 78-85, ISSN: 1388-9842, DOI: 10.1002/ejhf.961
European Journal of Heart Failure 20/1 2019-06-13
2017 Roberto Papait, Simone Serio, Christina Pagiatakis, Francesca Rusconi, Pierluigi Carullo, Marta Mazzola, Nicolò Salvarani, Michele Miragoli, Gianluigi Condorelli
Histone Methyltransferase G9a Is Required for Cardiomyocyte Homeostasis and Hypertrophy
published pages: 1233-1246, ISSN: 0009-7322, DOI: 10.1161/CIRCULATIONAHA.117.028561
Circulation 136/13 2019-06-13
2017 Veronica Larcher, Paolo Kunderfranco, Marco Vacchiano, Pierluigi Carullo, Marco Erreni, Irene Salamon, Federico Simone Colombo, Enrico Lugli, Marta Mazzola, Achille Anselmo, Gianluigi Condorelli
An autofluorescence-based method for the isolation of highly purified ventricular cardiomyocytes
published pages: 409-416, ISSN: 0008-6363, DOI: 10.1093/cvr/cvx239
Cardiovascular Research 114/3 2019-06-13
2018 Leonardo Elia, Paolo Kunderfranco, Pierluigi Carullo, Marco Vacchiano, Floriana Maria Farina, Ignacio Fernando Hall, Stefano Mantero, Cristina Panico, Roberto Papait, Gianluigi Condorelli, Manuela Quintavalle
UHRF1 epigenetically orchestrates smooth muscle cell plasticity in arterial disease
published pages: 2473-2486, ISSN: 0021-9738, DOI: 10.1172/JCI96121
Journal of Clinical Investigation 128/6 2019-06-13

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