Evidence map›Paper›PMID 36109561›Full record

ArticleScientific reports2022

PARP3 supervises G9a-mediated repression of adhesion and hypoxia-responsive genes in glioblastoma cells.

Leonel Nguekeu-Zebaze, Najat Hanini, Aurélia Noll, Nadège Wadier, Jean-Christophe Amé, Lisa Roegel, Françoise Dantzer

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
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  5. BKScientific reports · 2025
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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

7 authors at 2 institutions in 1 country.

Leonel Nguekeu-ZebazePoly(ADP-Ribosyl)Ation and Genome Integrity, Strasbourg Drug Discovery and Development Institute (IMS), UMR7242, Centre Nationale de la Recherche Scientifique/Université de Strasbourg, Institut de Recherche de l'Ecole de Biotechnologie de Strasbourg, 300 Bld. S. Brant, CS10413, 67412, Illkirch, France.
Najat HaniniPoly(ADP-Ribosyl)Ation and Genome Integrity, Strasbourg Drug Discovery and Development Institute (IMS), UMR7242, Centre Nationale de la Recherche Scientifique/Université de Strasbourg, Institut de Recherche de l'Ecole de Biotechnologie de Strasbourg, 300 Bld. S. Brant, CS10413, 67412, Illkirch, France.
Aurélia NollPoly(ADP-Ribosyl)Ation and Genome Integrity, Strasbourg Drug Discovery and Development Institute (IMS), UMR7242, Centre Nationale de la Recherche Scientifique/Université de Strasbourg, Institut de Recherche de l'Ecole de Biotechnologie de Strasbourg, 300 Bld. S. Brant, CS10413, 67412, Illkirch, France.
Nadège WadierPoly(ADP-Ribosyl)Ation and Genome Integrity, Strasbourg Drug Discovery and Development Institute (IMS), UMR7242, Centre Nationale de la Recherche Scientifique/Université de Strasbourg, Institut de Recherche de l'Ecole de Biotechnologie de Strasbourg, 300 Bld. S. Brant, CS10413, 67412, Illkirch, France.
Jean-Christophe AméPoly(ADP-Ribosyl)Ation and Genome Integrity, Strasbourg Drug Discovery and Development Institute (IMS), UMR7242, Centre Nationale de la Recherche Scientifique/Université de Strasbourg, Institut de Recherche de l'Ecole de Biotechnologie de Strasbourg, 300 Bld. S. Brant, CS10413, 67412, Illkirch, France.
Lisa RoegelPoly(ADP-Ribosyl)Ation and Genome Integrity, Strasbourg Drug Discovery and Development Institute (IMS), UMR7242, Centre Nationale de la Recherche Scientifique/Université de Strasbourg, Institut de Recherche de l'Ecole de Biotechnologie de Strasbourg, 300 Bld. S. Brant, CS10413, 67412, Illkirch, France.
Françoise DantzerPoly(ADP-Ribosyl)Ation and Genome Integrity, Strasbourg Drug Discovery and Development Institute (IMS), UMR7242, Centre Nationale de la Recherche Scientifique/Université de Strasbourg, Institut de Recherche de l'Ecole de Biotechnologie de Strasbourg, 300 Bld. S. Brant, CS10413, 67412, Illkirch, France. francoise.dantzer@unistra.fr.
Université de Strasbourg · FRBiotechnologie et Signalisation Cellulaire · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In breast cancer, Poly(ADP-ribose) polymerase 3 (PARP3) has been identified as a key driver of tumor aggressiveness exemplifying its selective inhibition as a promising surrogate for clinical activity onto difficult-to-treat cancers. Here we explored the role of PARP3 in the oncogenicity of glioblastoma, the most aggressive type of brain cancer. The absence of PARP3 did not alter cell proliferation nor the in vivo tumorigenic potential of glioblastoma cells. We identified a physical and functional interaction of PARP3 with the histone H3 lysine 9 methyltransferase G9a. We show that PARP3 helps to adjust G9a-dependent repression of the adhesion genes Nfasc and Parvb and the hypoxia-responsive genes Hif-2α, Runx3, Mlh1, Ndrg1, Ndrg2 and Ndrg4. Specifically for Nfasc, Parvb and Ndrg4, PARP3/G9a cooperate for an adjusted establishment of the repressive mark H3K9me2. While examining the functional consequence in cell response to hypoxia, we discovered that PARP3 acts to maintain the cytoskeletal microtubule stability. As a result, the absence of PARP3 markedly increases the sensitivity of glioblastoma cells to microtubule-destabilizing agents providing a new therapeutic avenue for PARP3 inhibition in brain cancer therapy.

Indexed as

Brain NeoplasmsGlioblastomaBasic Helix-Loop-Helix ProteinsCell Cycle ProteinsComplement C9HistonesHumansHypoxiaLysineMethyltransferasesPoly(ADP-ribose) PolymerasesTumor Suppressor ProteinsBasic Helix-Loop-Helix ProteinsCell Cycle ProteinsComplement C9HistonesLysineMethyltransferasesNDRG2 protein, humanPARP3 protein, humanPoly(ADP-ribose) PolymerasesTumor Suppressor Proteins

Identifiers

PMID36109561
PMCPMC9478127
OpenAlexW4295952210

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.