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CuHypMECH SIGNED

New Nuclear Medicine Imaging Radiotracer 64Cu(II) for diagnosing Hypoxia Conditions Based on the Cellular Copper Cycle

Total Cost €

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EC-Contrib. €

0

Partnership

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 CuHypMECH project word cloud

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

ratio    examined    signal    fdg    proteins    hot    mapping    therapy    selectivity    diagnose    cardiology    ed    spect    sites    copper    unmet    controversial    approved    form    consume    medicine    oxidising    imaging    reports    proprietary    angiogenesis    biophysical    radiotracers    radiotracer    systematic    proliferation    complexes    neurology    microenvironment    biomarker    incorporated    binding    tracers    tracer    malignant    quality    consumption    selective    metabolism    ct    18f    routinely    labelled    radio    pet    stability    stable    cold    drives    environment    encountered    bio    selectively    background    cycle    vivo    assimilates    tumours    64cu    isotopes    metabolic    oncology    multidisciplinary    discovery    structural    emphasising    chemistry    tumour    clinically    body    until    nutritional    efforts    marker    biology    glucose    mechanism    transfer    disease    despite    visualisation    hypoxia    clinical    functional    specificity    cellular    limits    owing    nuclear    resistance    metal   

Project "CuHypMECH" data sheet

The following table provides information about the project.

Coordinator
BAR ILAN UNIVERSITY 

Organization address
address: BAR ILAN UNIVERSITY CAMPUS
city: RAMAT GAN
postcode: 52900
website: www.biu.ac.il

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 Israel [IL]
 Total cost 1˙499˙345 €
 EC max contribution 1˙499˙345 € (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 2017-09-01   to  2022-08-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    BAR ILAN UNIVERSITY IL (RAMAT GAN) coordinator 1˙499˙345.00

Map

 Project objective

Imaging of hypoxia is important in many disease states in oncology, cardiology, and neurology. Hypoxia is a common condition encountered within the tumour microenvironment that drives proliferation, angiogenesis, and resistance to therapy. Despite on-going efforts to identify hypoxia, until now there is no clinically approved imaging biomarker, due to both low tumour uptake, and a low signal to background (S/B) ratio that affects the imaging quality. Nuclear Medicine is using labelled radio-isotopes for PET/CT and SPECT imaging. These radio-tracers diagnose the metabolic processes in the body. Among these tracers, 18F-FDG is the most routinely used as a marker of glucose metabolism. However, not all tumours consume glucose, and glucose consumption is not specific only for malignant tumours, which limits its application. Copper is a nutritional metal, recently examined as a radiotracer for hypoxia, owing to its to the oxidising environment. Clinical and in-vivo studies on various 64Cu(II)-PET radiotracers resulted in controversial reports on the specificity of the current tracers for hypoxia imaging due to non-selective bio-distribution & low S/B ratio. This multidisciplinary proposal focuses on the discovery of comprehensive signal pathways of the cellular copper cycle using advanced biophysical methods and a proprietary design of 64Cu(II) radiotracer. This radiotracer will be incorporated in the cellular copper cycle, and will enable to selectively target the oxidising environment in tumours. The design of the new radiotracer is based on systematic structural & functional mapping of the copper binding sites to the various copper proteins and the visualisation of the transfer mechanism. This new copper tracer should increase the selectivity of tumour uptake, stability, and improve bio-distribution. This project assimilates cold and hot chemistry and biology, while emphasising the clinical unmet need in metal based radiotracer that form stable complexes.

 Publications

year authors and title journal last update
List of publications.
2019 Zena Qasem, Matic Pavlin, Ida Ritacco, Lada Gevorkyan-Airapetov, Alessandra Magistrato, Sharon Ruthstein
The pivotal role of MBD4–ATP7B in the human Cu( i ) excretion path as revealed by EPR experiments and all-atom simulations
published pages: 1288-1297, ISSN: 1756-5901, DOI: 10.1039/C9MT00067D
Metallomics 11/7 2020-04-24
2019 Pavlin, Qasem, Sameach, Gevorkyan-Airapetov, Ritacco, Ruthstein, Magistrato
Unraveling the Impact of Cysteine-to-Serine Mutations on the Structural and Functional Properties of Cu(I)-Binding Proteins
published pages: 3462, ISSN: 1422-0067, DOI: 10.3390/ijms20143462
International Journal of Molecular Sciences 20/14 2020-04-24
2019 Alessandra Magistrato, Matic Pavlin, Zena Qasem, Sharon Ruthstein
Copper trafficking in eukaryotic systems: current knowledge from experimental and computational efforts
published pages: 26-33, ISSN: 0959-440X, DOI: 10.1016/j.sbi.2019.05.002
Current Opinion in Structural Biology 58 2020-04-24
2018 Ruthstein, Sharon; Shenberger, Yulia
COPPER-CONTAINING COMPLEX AND USES THEREOF
published pages: , ISSN: , DOI: 10.5281/zenodo.3244872
PCT-IL 2 2020-04-24
2018 Yulia Shenberger, Ortal Marciano, Hugo E. Gottlieb, Sharon Ruthstein
Insights into the N-terminal Cu(II) and Cu(I) binding sites of the human copper transporter CTR1
published pages: 1985-2002, ISSN: 0095-8972, DOI: 10.1080/00958972.2018.1492717
Journal of Coordination Chemistry 71/11-13 2019-05-22

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

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