Evidence map›Paper›PMID 40243560›Full record

ReviewInternational journal of molecular sciences2025

Proteasome Inhibitors: Potential in Rheumatoid Arthritis Therapy?

Oktávia Tarjányi, Katalin Olasz, Fanni Rátky, György Sétáló, Ferenc Boldizsár

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Proteasome: Role in T Cell Function Regulation.International journal of biological sciences · 2025
    Review
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

5 authors.

Oktávia TarjányiDepartment of Medical Biology, Medical School, University of Pecs, H-7624 Pecs, Hungary.ORCID 0000-0003-4702-4096
Katalin OlaszDepartment of Immunology and Biotechnology, Medical School, University of Pecs, H-7624 Pecs, Hungary.
Fanni RátkyDepartment of Medical Biology, Medical School, University of Pecs, H-7624 Pecs, Hungary.
György SétálóDepartment of Medical Biology, Medical School, University of Pecs, H-7624 Pecs, Hungary.ORCID 0000-0002-2901-8541
Ferenc BoldizsárDepartment of Immunology and Biotechnology, Medical School, University of Pecs, H-7624 Pecs, Hungary.ORCID 0000-0001-7831-1018

Funding

Ministry of Culture and Innovation of Hungary from the National Research, Development and In-novation Fund TKP2021-EGA-10
6 · The paper itself

Abstract

Rheumatoid arthritis (RA) is a chronic autoimmune disease that leads to the destruction of peripheral joint cartilage and bone tissue. Despite the advent of biological therapies in the past decades, the complete remission of RA patients is still out of reach. Therefore, the search for novel therapeutic approaches is still open in the field of RA. Proteasome inhibitors (PIs) were originally designed to be used in hematological malignancies like multiple myeloma. However, evidence has shown that they are potent inhibitors of the NF-κB pathway, which plays a pivotal role in inflammatory processes and RA. Furthermore, inhibition of cell activation and induction of apoptosis was also reported about PIs. In the present review, we summarize the current knowledge about the potential effects of PIs in RA based on reports from animal and human studies. We believe that there is substantial potential in the use of PIs in RA therapy either alone or in combination with the medications already used.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidProteasome InhibitorsAnimalsApoptosisHumansNF-kappa BSignal TransductionAntirheumatic AgentsNF-kappa BProteasome Inhibitorsproteasome inhibitorsrheumatoid arthritis therapy

Identifiers

PMID40243560
PMCPMC11988683

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.