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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.

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

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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