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PRINT-CHEMO SIGNED

To develop 3D bioPRINTed osteoinductive constructs that deliver CHEMOtherapeutics within large bone defects that are surgically created when removing bone tumours.

Total Cost €

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EC-Contrib. €

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Partnership

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 PRINT-CHEMO project word cloud

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

chemo    progress    relatively    dose    body    disease    suppressive    radiation    diagnosis    understand    caused    osteosarcoma    heterogeneity    systemic    printing    tibia    aberration    outcome    tumour    cells    clones    chemotherapy    damaged    costly    patients    adolescents    assembled    gene    15    made    femur    predominantly    treatment    metaphysis    18    diagnosed    hypothesis    regenerate    aged    exercise    young    last    loaded    subset    resistant    first    tumours    evolutionary    treat    45    50    usa    bones       approximately    rate    61    nanoparticles    surviving    dendritic    tissue    age    24    pattern    print    standard    united    therapy    diseased    adjuvant    initial    chemotherapeutics    cues    proximal    self    localised    relapse    drug    wave    distal    time    trying    rates    molecular    3d    mir    initiates    gold    14    socioeconomic    billion    children    resection    survival    194    bone    humerus   

Project "PRINT-CHEMO" data sheet

The following table provides information about the project.

Coordinator
THE PROVOST, FELLOWS, FOUNDATION SCHOLARS & THE OTHER MEMBERS OF BOARD OF THE COLLEGE OF THE HOLY & UNDIVIDED TRINITY OF QUEEN ELIZABETH NEAR DUBLIN 

Organization address
address: College Green
city: DUBLIN
postcode: 2
website: www.tcd.ie

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 Ireland [IE]
 Total cost 257˙561 €
 EC max contribution 257˙561 € (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-GF
 Starting year 2019
 Duration (year-month-day) from 2019-07-01   to  2022-06-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    THE PROVOST, FELLOWS, FOUNDATION SCHOLARS & THE OTHER MEMBERS OF BOARD OF THE COLLEGE OF THE HOLY & UNDIVIDED TRINITY OF QUEEN ELIZABETH NEAR DUBLIN IE (DUBLIN) coordinator 257˙561.00
2    THE BRIGHAM AND WOMEN'S HOSPITAL INC US (BOSTON MA) partner 0.00

Map

 Project objective

Osteosarcoma is the most commonly diagnosed bone tumour with most of these cases being in children and adolescents. Each year over 4,000 new cases of osteosarcoma are diagnosed in the United States. Osteosarcoma predominantly initiates in the metaphysis of long bones, such as the distal femur, proximal tibia and proximal humerus. Over 50% of these tumours are relatively resistant to radiation therapy, due to the molecular aberration of the tumour. The current gold standard for treatment is tumour resection and adjuvant chemotherapy, with a 5-year survival rate of 61.6% in patients aged 0-24 years old. Approximately one-third of patients diagnosed with osteosarcoma are expected to have a relapse, with only 15% of these patients surviving the disease a second time. Therefore, due to the young age of initial diagnosis, the management of this disease is a challenging and costly exercise, which has a significant socioeconomic cost, estimated to be €14.7 billion in Europe and $45 billion in the USA in the last 18 years. While significant progress has been made in trying to understand the intra-tumour heterogeneity and the evolutionary pattern of a subset of clones within the tumour, thus far, no major changes in treatment and outcome have been achieved. The hypothesis of PRINT-CHEMO is that localised delivery of self-assembled dendritic nanoparticles used as a first wave of treatment to deliver miR-194, a tumour suppressive gene, to the cells along with the delivery of nanoparticles loaded with chemotherapeutics would lead to higher survival rates and less side effects than systemic delivery of a higher dose of drug. Furthermore, PRINT-CHEMO not only aims to treat the diseased tissue but using 3D printing provide the necessary cues to allow for the body to regenerate the damaged bone caused due to tumour resection.

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The information about "PRINT-CHEMO" are provided by the European Opendata Portal: CORDIS opendata.

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