Evidence map›Paper›PMID 38383861›Full record

ArticleEMBO reports2024

IRE1 RNase controls CD95-mediated cell death.

Diana Pelizzari-Raymundo, Victoria Maltret, Manon Nivet, Raphael Pineau, Alexandra Papaioannou, Xingchen Zhou, Flavie Caradec, Sophie Martin, Matthieu Le Gallo, Tony Avril and 2 more

Open access · diamondAbstract read
In one paragraph

Article in EMBO reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

12 citing papers in PubMed, 10 citations in OpenAlex.

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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

12 authors at 1 institution in 1 country.

Diana Pelizzari-RaymundoInserm U1242, University of Rennes, Rennes, France.ORCID 0000-0002-9071-2380
Victoria Maltret *Inserm U1242, University of Rennes, Rennes, France.
Manon Nivet *Inserm U1242, University of Rennes, Rennes, France.ORCID 0000-0001-8562-9614
Raphael PineauInserm U1242, University of Rennes, Rennes, France.
Alexandra PapaioannouInserm U1242, University of Rennes, Rennes, France.ORCID 0000-0002-3470-284X
Xingchen ZhouInserm U1242, University of Rennes, Rennes, France.ORCID 0000-0003-2291-8181
Flavie CaradecInserm U1242, University of Rennes, Rennes, France.
Sophie MartinInserm U1242, University of Rennes, Rennes, France.ORCID 0000-0001-5173-6665
Matthieu Le GalloInserm U1242, University of Rennes, Rennes, France.ORCID 0000-0001-9085-8155
Tony AvrilInserm U1242, University of Rennes, Rennes, France.ORCID 0000-0002-1129-8514
Eric ChevetInserm U1242, University of Rennes, Rennes, France.ORCID 0000-0001-5855-4522
Elodie LafontInserm U1242, University of Rennes, Rennes, France. elodie.lafont@inserm.fr.ORCID 0000-0003-1978-7491
Inserm · FR

Funding

Association La Josselinaise des femmes N/AAssociation La Vannetaise N/ACentre Eugène Marquis N/AEC | H2020 | PRIORITY 'Excellent science' | H2020 Marie Skłodowska-Curie Actions (MSCA) ITN-675448Fondation ARC pour la Recherche sur le Cancer (ARC) PDF20171206671Fondation ARC pour la Recherche sur le Cancer (ARC) PJA20181207700Fondation de France (Foundation of France) N/AInstitut National Du Cancer (INCa) PLBIO 2018,2019Ligue Contre le Cancer (French League Against Cancer) N/AUniversité de Rennes 1 (University of Rennes 1) Défis Scientifiques
6 · The paper itself

Abstract

Signalling by the Unfolded Protein Response (UPR) or by the Death Receptors (DR) are frequently activated towards pro-tumoral outputs in cancer. Herein, we demonstrate that the UPR sensor IRE1 controls the expression of the DR CD95/Fas, and its cell death-inducing ability. Both genetic and pharmacologic blunting of IRE1 activity increased CD95 expression and exacerbated CD95L-induced cell death in glioblastoma (GB) and Triple-Negative Breast Cancer (TNBC) cell lines. In accordance, CD95 mRNA was identified as a target of Regulated IRE1-Dependent Decay of RNA (RIDD). Whilst CD95 expression is elevated in TNBC and GB human tumours exhibiting low RIDD activity, it is surprisingly lower in XBP1s-low human tumour samples. We show that IRE1 RNase inhibition limited CD95 expression and reduced CD95-mediated hepatic toxicity in mice. In addition, overexpression of XBP1s increased CD95 expression and sensitized GB and TNBC cells to CD95L-induced cell death. Overall, these results demonstrate the tight IRE1-mediated control of CD95-dependent cell death in a dual manner through both RIDD and XBP1s, and they identify a novel link between IRE1 and CD95 signalling.

Indexed as

RibonucleasesTriple Negative Breast NeoplasmsAnimalsCell DeathEndoribonucleasesFas Ligand ProteinHumansMiceProtein Serine-Threonine KinasesUnfolded Protein ResponseEndoribonucleasesFas Ligand ProteinProtein Serine-Threonine KinasesRibonucleasesCD95Cell DeathER StressIRE1Unfolded Protein Response

Identifiers

PMID38383861
PMCPMC11014915
OpenAlexW4392004768

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.