Evidence map›Paper›PMID 28186131›Full record

ArticleLeukemia2017

RECQ1 helicase is involved in replication stress survival and drug resistance in multiple myeloma.

E Viziteu, B Klein, J Basbous, Y-L Lin, C Hirtz, C Gourzones, L Tiers, A Bruyer, L Vincent, C Grandmougin and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Leukemia, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

52 citing papers in PubMed, 74 citations in OpenAlex.

  1. Article
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  6. Review
  7. Targeting chromosomal instability in patients with cancer.Nature reviews. Clinical oncology · 2024
    Review
  8. Oncoimmunology · 2024
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. RecQ Helicase Somatic Alterations in Cancer.Frontiers in molecular biosciences · 2022
    Review
  19. Review
  20. 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

16 authors at 3 institutions in 2 countries.

E ViziteuInstitute of Human Genetics, UMR 9002, CNRS and University of Montpellier, Montpellier, France.
B KleinInstitute of Human Genetics, UMR 9002, CNRS and University of Montpellier, Montpellier, France.
J BasbousInstitute of Human Genetics, UMR 9002, CNRS and University of Montpellier, Montpellier, France.
Y-L LinInstitute of Human Genetics, UMR 9002, CNRS and University of Montpellier, Montpellier, France.
C HirtzClinical Proteomic Platform, CHU Montpellier, Montpellier, France.
C GourzonesInstitute of Human Genetics, UMR 9002, CNRS and University of Montpellier, Montpellier, France.
L TiersClinical Proteomic Platform, CHU Montpellier, Montpellier, France.
A BruyerInstitute of Human Genetics, UMR 9002, CNRS and University of Montpellier, Montpellier, France.
L VincentDepartment of Clinical Hematology, CHU Montpellier, Montpellier, France.ORCID 0000-0001-5904-1286
C GrandmouginInstitute of Human Genetics, UMR 9002, CNRS and University of Montpellier, Montpellier, France.
A SeckingerMedizinische Klinik und Poliklinik V, Universitätsklinikum Heidelberg, Heidelberg, Germany.
H GoldschmidtMedizinische Klinik und Poliklinik V, Universitätsklinikum Heidelberg, Heidelberg, Germany.
A ConstantinouInstitute of Human Genetics, UMR 9002, CNRS and University of Montpellier, Montpellier, France.
P PaseroInstitute of Human Genetics, UMR 9002, CNRS and University of Montpellier, Montpellier, France.
D HoseMedizinische Klinik und Poliklinik V, Universitätsklinikum Heidelberg, Heidelberg, Germany.
J MoreauxInstitute of Human Genetics, UMR 9002, CNRS and University of Montpellier, Montpellier, France.ORCID 0000-0002-5717-3207
Centre National de la Recherche Scientifique · FRCentre Hospitalier Universitaire de Montpellier · FRHeidelberg University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma (MM) is a plasma cell cancer with poor survival, characterized by the expansion of multiple myeloma cells (MMCs) in the bone marrow. Using a microarray-based genome-wide screen for genes responding to DNA methyltransferases (DNMT) inhibition in MM cells, we identified RECQ1 among the most downregulated genes. RecQ helicases are DNA unwinding enzymes involved in the maintenance of chromosome stability. Here we show that RECQ1 is significantly overexpressed in MMCs compared to normal plasma cells and that increased RECQ1 expression is associated with poor prognosis in three independent cohorts of patients. Interestingly, RECQ1 knockdown inhibits cells growth and induces apoptosis in MMCs. Moreover, RECQ1 depletion promotes the development of DNA double-strand breaks, as evidenced by the formation of 53BP1 foci and the phosphorylation of ataxia-telangiectasia mutated (ATM) and histone variant H2A.X (H2AX). In contrast, RECQ1 overexpression protects MMCs from melphalan and bortezomib cytotoxicity. RECQ1 interacts with PARP1 in MMCs exposed to treatment and RECQ1 depletion sensitizes MMCs to poly(ADP-ribose) polymerase (PARP) inhibitor. DNMT inhibitor treatment results in RECQ1 downregulation through miR-203 deregulation in MMC. Altogether, these data suggest that association of DNA damaging agents and/or PARP inhibitors with DNMT inhibitors may represent a therapeutic approach in patients with high RECQ1 expression associated with a poor prognosis.

Indexed as

BortezomibCell CycleDNA Breaks, Double-StrandedDNA-Cytosine MethylasesDNA DamageDNA MethylationDNA, NeoplasmDNA ReplicationDrug Resistance, NeoplasmEnzyme InductionEnzyme InhibitorsGene Expression Regulation, NeoplasticHumansMelphalanMicroRNAsMolecular Targeted TherapyBortezomibDNA-Cytosine MethylasesDNA, NeoplasmEnzyme InhibitorsMelphalanMicroRNAsMIRN203 microRNA, humanNeoplasm ProteinsPARP1 protein, humanPoly (ADP-Ribose) Polymerase-1RecQ HelicasesRECQL protein, humanRNA, Small Interfering

Identifiers

PMID28186131
PMCPMC5629372
OpenAlexW2587042021

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.