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20SInhibitor SIGNED

Selective 20S proteasome inhibition for multiple myeloma therapy

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 20SInhibitor project word cloud

Explore the words cloud of the 20SInhibitor project. It provides you a very rough idea of what is the project "20SInhibitor" about.

networks    designed    molecules    therapy    business    20    revealed    catalytic    later    mcl    blood    chymotrypsin    basis    inhibiting    mantle    structural    compounds    cancer    plasma    inhibit    risk    position    chance    motif    regulators    approval    ip    perspective    lower    intervention    equip    proteins    cell    receiving    reduce    light    pharmaceutical    strategy    contacts    myeloma    regimens    minimize    ccrs    peptides    switched    anticipate    26s    mainstay    protection    inhibitors    direction    toxicity    innovation    therapeutics    protein    industry    drugs    pis    preliminary    first    regulatory    cells    mm    core    therapeutic    drug    laboratory    treatment    peptide    proteasome    peptidomimetic    small    termed    sufficient    form    artificial    incurable    sequence    initial    deleterious    companies    multiple    50    attractive    proteasomes    family    synthetic    actions    lymphoma    revisit    specificity    carry    pose    selectively    selective    20s    commercialization    probability   

Project "20SInhibitor" data sheet

The following table provides information about the project.

Coordinator
WEIZMANN INSTITUTE OF SCIENCE 

Organization address
address: HERZL STREET 234
city: REHOVOT
postcode: 7610001
website: www.weizmann.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 150˙000 €
 EC max contribution 150˙000 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-PoC
 Funding Scheme ERC-POC
 Starting year 2019
 Duration (year-month-day) from 2019-04-01   to  2020-09-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    WEIZMANN INSTITUTE OF SCIENCE IL (REHOVOT) coordinator 150˙000.00

Map

 Project objective

Multiple myeloma (MM) is a cancer of plasma cells, that is incurable, and the second most common form of blood cancer. Proteasome inhibitors (PIs) are considered a mainstay in the treatment of MM and mantle cell lymphoma (MCL). Current drugs, based on PIs however, target the chymotrypsin-like activity of the 20S proteasome, and inhibit the activities of both the 20S and 26S proteasomes. Thus, it is possible that selective drug intervention specifically inhibiting only the 20S proteasomes will reduce toxicity, and minimize the deleterious side effects of the current therapeutic regimens.

Our preliminary work revealed a family of 20S proteasome inhibitors, which we termed Catalytic Core Regulators (CCRs) that selectively target the 20S proteasome rather than the 26S complex. Based on sequence motif and structural elements of the CCRs we have designed an artificial protein that is capable of inhibiting the 20S proteasome. We anticipate that these findings will lead to the design of synthetic proteins, peptides or peptidomimetic compounds targeting cancer cells more specifically. This specificity will pose the compounds in an attractive light for using them in various therapeutic applications.

What is exciting from the commercialization perspective, is that pharmaceutical research has switched to revisit the use of peptides as therapeutics. Pharmaceutical companies have seen the development of peptides as a promising direction to lower their risk position. Overall, peptide therapeutics have a 20% chance of receiving regulatory approval, a probability that is 50% higher than that for the approval of small molecules, which form the basis of so called traditional drugs.

In the project, we will carry out actions, which will equip us with the sufficient IP protection strategy, business strategy, industry networks and initial contacts for taking the innovation out from the laboratory to next phase in developing therapy first for MM and MCL later on.

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The information about "20SINHIBITOR" are provided by the European Opendata Portal: CORDIS opendata.

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