Evidence map›Paper›PMID 34067602›Full record

ReviewCancers2021

Targeting Reactive Oxygen Species Metabolism to Induce Myeloma Cell Death.

Mélody Caillot, Hassan Dakik, Frédéric Mazurier, Brigitte Sola

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

30 citing papers in PubMed, 28 citations in OpenAlex.

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  10. Transmetalation in Cancer Pharmacology.International journal of molecular sciences · 2025
    Review
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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

4 authors at 2 institutions in 1 country.

Mélody CaillotNormandie University, INSERM, Université de Caen, F-14000 Caen, France.ORCID 0000-0001-7591-4665
Hassan DakikUniversité de Tours, GICC EA7501, CNRS, F-3700 Tours, France.ORCID 0000-0003-0270-8195
Frédéric MazurierUniversité de Tours, GICC EA7501, CNRS, F-3700 Tours, France.ORCID 0000-0002-6984-7096
Brigitte SolaNormandie University, INSERM, Université de Caen, F-14000 Caen, France.ORCID 0000-0001-7278-9651
Inserm · FRUniversité de Tours · FR

Funding

Fondation Française de Recherche sur le Myélome et le MGUS (FFRMG) ROSE-AO2018Ligue contre le Cancer CD76-AO2018
6 · The paper itself

Abstract

Multiple myeloma (MM) is a common hematological disease characterized by the accumulation of clonal malignant plasma cells in the bone marrow. Over the past two decades, new therapeutic strategies have significantly improved the treatment outcome and patients survival. Nevertheless, most MM patients relapse underlying the need of new therapeutic approaches. Plasma cells are prone to produce large amounts of immunoglobulins causing the production of intracellular ROS. Although adapted to high level of ROS, MM cells die when exposed to drugs increasing ROS production either directly or by inhibiting antioxidant enzymes. In this review, we discuss the efficacy of ROS-generating drugs for inducing MM cell death and counteracting acquired drug resistance specifically toward proteasome inhibitors.

Indexed as

antioxidant enzymemitochondriamultiple myelomaNOXOXPHOSproteasome inhibitorredox balanceROS

Identifiers

PMID34067602
PMCPMC8156203
OpenAlexW3162416679

What OpenQuestion holds

Textmetadata
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.