Evidence map›Paper›PMID 27057635›Full record

ArticleOncotarget2016

Differential effects of lenalidomide during plasma cell differentiation.

Michel Jourdan, Maïlys Cren, Peter Schafer, Nicolas Robert, Christophe Duperray, Laure Vincent, Patrice Ceballos, Guillaume Cartron, Jean-François Rossi, Jérôme Moreaux and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. CD34International journal of hematology · 2022
    Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Molecular basis of clonal evolution in multiple myeloma.International journal of hematology · 2020
    Review
  12. Article
  13. Article
  14. Article
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

12 authors at 4 institutions in 1 country.

Michel JourdanINSERM, U1040, Montpellier, France.
Maïlys CrenINSERM, U1040, Montpellier, France.
Peter SchaferTranslational Development Department, Celgene Corporation, Summit, NJ, USA.
Nicolas RobertCHU Montpellier, Laboratory for Monitoring Innovative Therapies, Department of Biological Hematology, Montpellier, France.
Christophe DuperrayCytometry IRB, Montpellier Rio Imaging, Montpellier, France.
Laure VincentCHU Montpellier, Department of Clinical Hematology, Montpellier, France.
Patrice CeballosCHU Montpellier, Department of Clinical Hematology, Montpellier, France.
Guillaume CartronCHU Montpellier, Department of Clinical Hematology, Montpellier, France.
Jean-François RossiCHU Montpellier, Department of Clinical Hematology, Montpellier, France.
Jérôme MoreauxCNRS UPR1142, Institute of Human Genetics, Montpellier, France.
Rajesh ChopraTranslational Development Department, Celgene Corporation, Summit, NJ, USA.
Bernard KleinCNRS UPR1142, Institute of Human Genetics, Montpellier, France.
Centre Hospitalier Universitaire de Montpellier · FRUniversité de Montpellier · FRCentre National de la Recherche Scientifique · FRInserm · FR

Funding

Cancer Research UK 11566
6 · The paper itself

Abstract

Thalidomide, lenalidomide and pomalidomide have greatly improved the outcome of patients with multiple myeloma. However, their effects on plasma cells, the healthy counterpart of myeloma cells, are unknown. Here, we investigated lenalidomide effects on normal human plasma cell generation using an in vitro model. Lenalidomide inhibited the generation of pre-plasmablasts and early plasma cells, while it moderately affected plasmablast production. It also reduced the expression level of Ikaros, Aiolos, and IRF4 transcription factors, in plasmablasts and early plasma cells. This suggests that their differential sensitivity to lenalidomide is not due to a difference in Ikaros or Aiolos degradation. Lenalidomide also inhibited long-lived plasma cell generation, but did not impair their long-term survival once generated. This last observation is in agreement with the finding that lenalidomide treatment for 3-18 months did not affect the bone marrow healthy plasma cell count in allografted patients with multiple myeloma. Our findings should prompt to investigate whether lenalidomide resistance in patients with multiple myeloma could be associated with the emergence of malignant plasmablasts or long-lived plasma cells that are less sensitive to lenalidomide.

Indexed as

Antineoplastic AgentsCell DifferentiationCells, CulturedHematopoietic Stem Cell TransplantationHumansLenalidomideMultiple MyelomaNeoplasm, ResidualPlasma CellsThalidomideAntineoplastic AgentsLenalidomideThalidomidedifferentiationIKZF1IKZF3lenalidomideplasma cell

Identifiers

PMID27057635
PMCPMC5053712
OpenAlexW2340439009

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.