Evidence map›Paper›PMID 33126754›Full record

ReviewInternational journal of molecular sciences2020

Role of Polycomb Complexes in Normal and Malignant Plasma Cells.

Emmanuel Varlet, Sara Ovejero, Anne-Marie Martinez, Giacomo Cavalli, Jerome Moreaux

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Structure and Function of the Polycomb Repressive Complexes PRC1 and PRC2.International journal of molecular sciences · 2022
    Article
  4. Review
  5. Article
  6. Insights into high-risk multiple myeloma from an analysis of the role of PHF19 in cancer.Journal of experimental & clinical cancer research : CR · 2021
    Review
  7. Article
  8. Article
  9. Comparing a Novel Malformation Syndrome Caused by Pathogenic Variants inFrontiers in cell and developmental biology · 2021
    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

5 authors at 2 institutions in 1 country.

Emmanuel VarletInstitute of Human Genetics, UMR 9002 Centre National de la Recherche Scientifique, University of Montpellier, Montpellier, 34396 Montpellier, France.
Sara OvejeroInstitute of Human Genetics, UMR 9002 Centre National de la Recherche Scientifique, University of Montpellier, Montpellier, 34396 Montpellier, France.ORCID 0000-0002-8354-856X
Anne-Marie MartinezInstitute of Human Genetics, UMR 9002 Centre National de la Recherche Scientifique, University of Montpellier, Montpellier, 34396 Montpellier, France.ORCID 0000-0001-8562-7627
Giacomo CavalliInstitute of Human Genetics, UMR 9002 Centre National de la Recherche Scientifique, University of Montpellier, Montpellier, 34396 Montpellier, France.
Jerome MoreauxInstitute of Human Genetics, UMR 9002 Centre National de la Recherche Scientifique, University of Montpellier, Montpellier, 34396 Montpellier, France.ORCID 0000-0002-5717-3207
Université de Montpellier · FRInstitut Universitaire de France · FR

Funding

Agence Nationale de la Recherche ANR-18-CE15-0010-01 PLASMADIFF-3DAgence Nationale de la Recherche TIE-Skip; 2017-CE15-0024-01Institut National Du Cancer PLBIO18-362 PIT-MMInstitut National Du Cancer PLBIO19-098 INCA_13832
6 · The paper itself

Abstract

Plasma cells (PC) are the main effectors of adaptive immunity, responsible for producing antibodies to defend the body against pathogens. They are the result of a complex highly regulated cell differentiation process, taking place in several anatomical locations and involving unique genetic events. Pathologically, PC can undergo tumorigenesis and cause a group of diseases known as plasma cell dyscrasias, including multiple myeloma (MM). MM is a severe disease with poor prognosis that is characterized by the accumulation of malignant PC within the bone marrow, as well as high clinical and molecular heterogeneity. MM patients frequently develop resistance to treatment, leading to relapse. Polycomb group (PcG) proteins are epigenetic regulators involved in cell fate and carcinogenesis. The emerging roles of PcG in PC differentiation and myelomagenesis position them as potential therapeutic targets in MM. Here, we focus on the roles of PcG proteins in normal and malignant plasma cells, as well as their therapeutic implications.

Indexed as

Cell DifferentiationHematopoiesisAnimalsHumansNeoplasmsPlasma CellsPolycomb-Group ProteinsPolycomb-Group Proteinsepigeneticsmultiple myelomaplasma cell differentiationpolycomb

Identifiers

PMID33126754
PMCPMC7662980
OpenAlexW3096809627

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.