Evidence map›Paper›PMID 34184733›Full record

ArticleBiology open2021

KDM5A and KDM5B histone-demethylases contribute to HU-induced replication stress response and tolerance.

Solenne Gaillard, Virginie Charasson, Cyril Ribeyre, Kader Salifou, Marie-Jeanne Pillaire, Jean-Sebastien Hoffmann, Angelos Constantinou, Didier Trouche, Marie Vandromme

Open access · goldAbstract read
In one paragraph

Article in Biology open, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

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  12. Layered evolution of gene expression in "superfast" muscles for courtship.Proceedings of the National Academy of Sciences of the United States of America · 2022
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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.

Solenne GaillardMCD, Centre de Biologie Integrative (CBI), University of Toulouse, CNRS, UPS, 31062 Toulouse, France.
Virginie CharassonMCD, Centre de Biologie Integrative (CBI), University of Toulouse, CNRS, UPS, 31062 Toulouse, France.
Cyril RibeyreInstitut de Génétique Humaine, CNRS, Université de Montpellier, Montpellier, France.ORCID 0000-0002-5146-0977
Kader SalifouInstitut de Génétique Humaine, CNRS, Université de Montpellier, Montpellier, France.
Marie-Jeanne PillaireCancer Research Center of Toulouse, INSERM U1037, CNRS ERL5294, University of Toulouse 3, 31037 Toulouse, France.
Jean-Sebastien HoffmannLaboratoire de Pathologie, Institut Universitaire du Cancer-Toulouse, Oncopole, 1 avenue Irène-Joliot-Curie, 31059 Toulouse cedex, France.
Angelos ConstantinouInstitut de Génétique Humaine, CNRS, Université de Montpellier, Montpellier, France.
Didier TroucheMCD, Centre de Biologie Integrative (CBI), University of Toulouse, CNRS, UPS, 31062 Toulouse, France.
Marie VandrommeMCD, Centre de Biologie Integrative (CBI), University of Toulouse, CNRS, UPS, 31062 Toulouse, France.ORCID 0000-0002-5675-7999
Centre National de la Recherche Scientifique · FRInstitut universitaire du cancer de Toulouse Oncopole · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

KDM5A and KDM5B histone-demethylases are overexpressed in many cancers and have been involved in drug tolerance. Here, we describe that KDM5A, together with KDM5B, contribute to replication stress (RS) response and tolerance. First, they positively regulate RRM2, the regulatory subunit of ribonucleotide reductase. Second, they are required for optimal levels of activated Chk1, a major player of the intra-S phase checkpoint that protects cells from RS. We also found that KDM5A is enriched at ongoing replication forks and associates with both PCNA and Chk1. Because RRM2 is a major determinant of replication stress tolerance, we developed cells resistant to HU, and show that KDM5A/B proteins are required for both RRM2 overexpression and tolerance to HU. Altogether, our results indicate that KDM5A/B are major players of RS management. They also show that drugs targeting the enzymatic activity of KDM5 proteins may not affect all cancer-related consequences of KDM5A/B overexpression.

Indexed as

Drug ToleranceCell Line, TumorCheckpoint Kinase 1DNA DamageDNA RepairDNA ReplicationGene Expression RegulationHistonesHumansHydroxyureaJumonji Domain-Containing Histone DemethylasesNuclear ProteinsRepressor ProteinsRetinoblastoma-Binding Protein 2Ribonucleoside Diphosphate ReductaseSignal TransductionCheckpoint Kinase 1CHEK1 protein, humanHistonesHydroxyureaJumonji Domain-Containing Histone DemethylasesKDM5A protein, humanKDM5B protein, humanNuclear ProteinsRepressor ProteinsRetinoblastoma-Binding Protein 2Ribonucleoside Diphosphate Reductaseribonucleotide reductase M2ChromatinDrug toleranceReplication stress

Identifiers

PMID34184733
PMCPMC8181900
OpenAlexW3164270558

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.