Evidence map›Paper›PMID 30925767›Full record

ArticleCancers2019

Antioxidant Defenses Confer Resistance to High Dose Melphalan in Multiple Myeloma Cells.

Claire Gourzones, Céline Bellanger, Sylvain Lamure, Ouissem Karmous Gadacha, Elvira Garcia De Paco, Laure Vincent, Guillaume Cartron, Bernard Klein, Jérôme Moreaux

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

17 citing papers in PubMed, 30 citations in OpenAlex.

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  14. Methods to Analyse Time-to-Event Data: The Kaplan-Meier Survival Curve.Oxidative medicine and cellular longevity · 2021
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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

9 authors at 2 institutions in 1 country.

Claire GourzonesIGH, CNRS, University of Montpellier, 34000 Montpellier, France. cgourzones@gmail.com.
Céline BellangerIGH, CNRS, University of Montpellier, 34000 Montpellier, France. Celine.Bellanger@univ-nantes.fr.
Sylvain LamureDepartment of Clinical Hematology, CHU Montpellier, 34395 Montpellier, France. s-lamure@chu-montpellier.fr.ORCID 0000-0001-5980-305X
Ouissem Karmous GadachaIGH, CNRS, University of Montpellier, 34000 Montpellier, France. ouissem.karmous-gadacha@igh.cnrs.fr.
Elvira Garcia De PacoIGH, CNRS, University of Montpellier, 34000 Montpellier, France. elvira.garcia-de-paco@igh.cnrs.fr.
Laure VincentDepartment of Clinical Hematology, CHU Montpellier, 34395 Montpellier, France. l-vincent@chu-montpellier.fr.ORCID 0000-0001-5904-1286
Guillaume CartronDepartment of Clinical Hematology, CHU Montpellier, 34395 Montpellier, France. g-cartron@chu-montpellier.fr.
Bernard KleinIGH, CNRS, University of Montpellier, 34000 Montpellier, France. bernard.klein@inserm.fr.
Jérôme MoreauxIGH, CNRS, University of Montpellier, 34000 Montpellier, France. jerome.moreaux@igh.cnrs.fr.ORCID 0000-0002-5717-3207
Centre National de la Recherche Scientifique · FRCentre Hospitalier Universitaire de Montpellier · FR

Funding

FP7 Health FP7-OVERMYRInstitut National Du Cancer INCa-DGOS-Inserm 6045Institut National Du Cancer MM&TTInstitut National Du Cancer PLBIO15-256
6 · The paper itself

Abstract

backgroundMultiple myeloma (MM) is the second most common hematological cancer after lymphoma. It is characterized by the accumulation of clonal malignant plasma cells within the bone marrow. The development of drug resistance remains a major problem for effective treatment of MM. Understand the mechanisms underlying drug resistance in MM is a focal point to improve MM treatment.

methodsIn the current study, we analyzed further the role of redox imbalance induction in melphalan-induced toxicity both in human myeloma cell lines (HMCLs) and primary myeloma cells from patients.

resultsWe developed an in-vitro model of short-term resistance to high-dose melphalan and identified that pretreatment with physiological concentration of GSH protects HMCLs from melphalan-induced cell cycle arrest and cytotoxicity. We validated these results using primary MM cells from patients co-cultured with their bone marrow microenvironment. GSH did not affect the ability of melphalan to induce DNA damages in MM cells. Interestingly, melphalan induced reactive oxygen species, a significant decrease in GSH concentration, protein and lipd oxydation together with NRF2 (NF-E2-related factor 2) pathway activation.

conclusionsOur data demonstrate that antioxidant defenses confers resistance to high dose melphalan in MM cells, supporting that redox status in MM cells could be determinant for patients' response to melphalan.

Indexed as

drug resistanceGSHmelphalanmultiple myelomaNRF2reactive oxygen species

Identifiers

PMID30925767
PMCPMC6521290
OpenAlexW2923914229

What OpenQuestion holds

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Registered trials

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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.