Evidence map›Paper›PMID 36771100›Full record

ReviewMolecules (Basel, Switzerland)2023

Natural Agents as Novel Potential Source of Proteasome Inhibitors with Anti-Tumor Activity: Focus on Multiple Myeloma.

Francesca Alessandra Ambrosio, Giosuè Costa, Maria Eugenia Gallo Cantafio, Roberta Torcasio, Francesco Trapasso, Stefano Alcaro, Giuseppe Viglietto, Nicola Amodio

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. 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

8 authors.

Francesca Alessandra AmbrosioDepartment of Experimental and Clinical Medicine, Campus "S. Venuta", University "Magna Græcia" of Catanzaro, Viale Europa, 88100 Catanzaro, Italy.ORCID 0000-0003-4874-2946
Giosuè CostaDepartment of Health Sciences, University "Magna Græcia" of Catanzaro, Campus "S. Venuta", Viale Europa, 88100 Catanzaro, Italy.ORCID 0000-0003-0947-9479
Maria Eugenia Gallo CantafioDepartment of Experimental and Clinical Medicine, Campus "S. Venuta", University "Magna Græcia" of Catanzaro, Viale Europa, 88100 Catanzaro, Italy.
Roberta TorcasioDepartment of Experimental and Clinical Medicine, Campus "S. Venuta", University "Magna Græcia" of Catanzaro, Viale Europa, 88100 Catanzaro, Italy.
Francesco TrapassoDepartment of Experimental and Clinical Medicine, Campus "S. Venuta", University "Magna Græcia" of Catanzaro, Viale Europa, 88100 Catanzaro, Italy.
Stefano AlcaroDepartment of Health Sciences, University "Magna Græcia" of Catanzaro, Campus "S. Venuta", Viale Europa, 88100 Catanzaro, Italy.
Giuseppe VigliettoDepartment of Experimental and Clinical Medicine, Campus "S. Venuta", University "Magna Græcia" of Catanzaro, Viale Europa, 88100 Catanzaro, Italy.
Nicola AmodioDepartment of Experimental and Clinical Medicine, Campus "S. Venuta", University "Magna Græcia" of Catanzaro, Viale Europa, 88100 Catanzaro, Italy.

Funding

Italian Association for Cancer Research IG24449Italian Ministry of Health GR-2016-02361523Ministry of Education, Universities and Research PRIN 2017 - 201744BN5T
6 · The paper itself

Abstract

Multiple myeloma (MM) is an aggressive and incurable disease for most patients, characterized by periods of treatment, remission and relapse. The introduction of new classes of drugs, such as proteasome inhibitors (PIs), has improved survival outcomes in these patient populations. The proteasome is the core of the ubiquitin-proteasome system (UPS), a complex and conserved pathway involved in the control of multiple cellular processes, including cell cycle control, transcription, DNA damage repair, protein quality control and antigen presentation. To date, PIs represent the gold standard for the treatment of MM. Bortezomib was the first PI approved by the FDA, followed by next generation of PIs, namely carfilzomib and ixazomib. Natural agents play an important role in anti-tumor drug discovery, and many of them have recently been reported to inhibit the proteasome, thus representing a new potential source of anti-MM drugs. Based on the pivotal biological role of the proteasome and on PIs' significance in the management of MM, in this review we aim to briefly summarize recent evidence on natural compounds capable of inhibiting the proteasome, thus triggering anti-MM activity.

Indexed as

Antineoplastic AgentsMultiple MyelomaBortezomibHumansProteasome Endopeptidase ComplexProteasome InhibitorsAntineoplastic AgentsBortezomibProteasome Endopeptidase ComplexProteasome Inhibitorsmultiple myelomanatural compoundsproteasomeproteasome inhibitors

Identifiers

PMID36771100
PMCPMC9919276

What OpenQuestion holds

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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.