Evidence map›Paper›PMID 35204815›Full record

ArticleBiomolecules2022

Insulin-Degrading Enzyme Is a Non Proteasomal Target of Carfilzomib and Affects the 20S Proteasome Inhibition by the Drug.

Grazia Raffaella Tundo, Diego Sbardella, Francesco Oddone, Giuseppe Grasso, Stefano Marini, Maria Grazia Atzori, Anna Maria Santoro, Danilo Milardi, Francesco Bellia, Gabriele Macari and 5 more

Open access · goldAbstract read
In one paragraph

Article in Biomolecules, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 31% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 6 institutions in 1 country.

Grazia Raffaella TundoIRCCS-Fondazione BIETTI, 00198 Rome, Italy.ORCID 0000-0002-3866-3171
Diego SbardellaIRCCS-Fondazione BIETTI, 00198 Rome, Italy.
Francesco OddoneIRCCS-Fondazione BIETTI, 00198 Rome, Italy.
Giuseppe GrassoDepartment of Chemical Science, University of Catania, 95125 Catania, Italy.ORCID 0000-0002-7179-4835
Stefano MariniDepartment of Clinical Sciences and Translational Medicine, University of Roma Tor Vergata, 00133 Rome, Italy.
Maria Grazia AtzoriDepartment of Systems Medicine, University of Rome Tor Vergata, 00133 Rome, Italy.
Anna Maria SantoroInstitute of Crystallography, CNR, 95126 Catania, Italy.
Danilo MilardiInstitute of Crystallography, CNR, 95126 Catania, Italy.ORCID 0000-0003-3940-9439
Francesco BelliaInstitute of Crystallography, CNR, 95126 Catania, Italy.ORCID 0000-0002-9273-5949
Gabriele MacariDepartment of Sciences, Rome Tre University, 00146 Rome, Italy.ORCID 0000-0001-7519-4418
Grazia GrazianiDepartment of Systems Medicine, University of Rome Tor Vergata, 00133 Rome, Italy.ORCID 0000-0002-0221-768X
Fabio PolticelliDepartment of Sciences, Rome Tre University, 00146 Rome, Italy.ORCID 0000-0002-7657-2019
Paolo CascioDepartment of Veterinary Sciences, University of Turin, 10095 Grugliasco, Italy.
Mariacristina ParravanoIRCCS-Fondazione BIETTI, 00198 Rome, Italy.
Massimo ColettaIRCCS-Fondazione BIETTI, 00198 Rome, Italy.
Fondazione G.B. Bietti · ITInstitute of Crystallography · ITUniversity of Rome Tor Vergata · ITRoma Tre University · ITUniversity of Catania · ITUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Carfilzomib is a last generation proteasome inhibitor (PI) with proven clinical efficacy in the treatment of relapsed/refractory multiple myeloma. This drug is considered to be extremely specific in inhibiting the chymotrypsin-like activity of the 20S proteasome, encoded by the β5 subunit, overcoming some bortezomib limitations, the first PI approved for multiple myeloma therapy which is however burdened by a significant toxicity profile, due also to its off-target effects. Here, molecular approaches coupled with molecular docking studies have been used to unveil that the Insulin-Degrading Enzyme, a ubiquitous and highly conserved Zn

Indexed as

Antineoplastic AgentsInsulysinMultiple MyelomaHumansMolecular Docking SimulationOligopeptidesPharmaceutical PreparationsProteasome Endopeptidase ComplexProteasome InhibitorsAntineoplastic AgentscarfilzomibInsulysinOligopeptidesPharmaceutical PreparationsProteasome Endopeptidase ComplexProteasome Inhibitorscancercarfilzomibinsulin-degrading enzymeneurodegenerationproteasome

Identifiers

PMID35204815
PMCPMC8869475
OpenAlexW4212838430

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.