Evidence map›Paper›PMID 25669983›Full record

ArticleOncotarget2015

Drug metabolism and clearance system in tumor cells of patients with multiple myeloma.

Wafa Hassen, Alboukadel Kassambara, Thierry Reme, Surinder Sahota, Anja Seckinger, Laure Vincent, Guillaume Cartron, Jérôme Moreaux, Dirk Hose, Bernard Klein

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

20 citing papers in PubMed, 26 citations in OpenAlex.

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  10. Distribution pattern of tumor infiltrating lymphocytes and tumor microenvironment composition as prognostic indicators in anorectal malignant melanoma.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 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

10 authors at 5 institutions in 4 countries.

Wafa HassenInstitute of Human Genetics, CNRS-UPR1142, Montpellier, France.
Alboukadel KassambaraInstitute of Human Genetics, CNRS-UPR1142, Montpellier, France.
Thierry RemeInstitute of Human Genetics, CNRS-UPR1142, Montpellier, France.
Surinder SahotaCancer Sciences Unit, Faculty of Medicine, University of Southampton, UK.
Anja SeckingerMedizinische Klinik V, Universitätsklinikum Heidelberg, Heidelberg, Germany.
Laure VincentCHU Montpellier, Department of Clinical Hematology, Montpellier, France.
Guillaume CartronCHU Montpellier, Department of Clinical Hematology, Montpellier, France.
Jérôme MoreauxInstitute of Human Genetics, CNRS-UPR1142, Montpellier, France.
Dirk HoseMedizinische Klinik V, Universitätsklinikum Heidelberg, Heidelberg, Germany.
Bernard KleinInstitute of Human Genetics, CNRS-UPR1142, Montpellier, France.
Centre Hospitalier Universitaire de Montpellier · FRCentre National de la Recherche Scientifique · FRNational Center for Tumor Diseases · DEInstitut de Génétique Humaine · FRUniversity of Southampton · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Resistance to chemotherapy is a major limitation of cancer treatments with several molecular mechanisms involved, in particular altered local drug metabolism and detoxification process. The role of drug metabolism and clearance system has not been satisfactorily investigated in Multiple Myeloma (MM), a malignant plasma cell cancer for which a majority of patients escapes treatment. The expression of 350 genes encoding for uptake carriers, xenobiotic receptors, phase I and II Drug Metabolizing Enzymes (DMEs) and efflux transporters was interrogated in MM cells (MMCs) of newly-diagnosed patients in relation to their event free survival. MMCs of patients with a favourable outcome have an increased expression of genes coding for xenobiotic receptors (RXRα, LXR, CAR and FXR) and accordingly of their gene targets, influx transporters and phase I/II DMEs. On the contrary, MMCs of patients with unfavourable outcome displayed a global down regulation of genes coding for xenobiotic receptors and the downstream detoxification genes but had a high expression of genes coding for ARNT and Nrf2 pathways and ABC transporters. Altogether, these data suggests ARNT and Nrf2 pathways could be involved in MM primary resistance and that targeting RXRα, PXR, LXR and FXR through agonists could open new perspectives to alleviate or reverse MM drug resistance.

Indexed as

Antineoplastic AgentsCarrier ProteinsDrug Resistance, MultipleHumansMultiple MyelomaPrognosisAntineoplastic AgentsCarrier Proteinsdrug metabolism and clearancemultiple myelomaprognosis

Identifiers

PMID25669983
PMCPMC4467447
OpenAlexW2134178574

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.