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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.

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

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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