Evidence map›Paper›PMID 29311133›Full record

ArticleEMBO molecular medicine2018

Dual IRE1 RNase functions dictate glioblastoma development.

Stéphanie Lhomond, Tony Avril, Nicolas Dejeans, Konstantinos Voutetakis, Dimitrios Doultsinos, Mari McMahon, Raphaël Pineau, Joanna Obacz, Olga Papadodima, Florence Jouan and 18 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 103 papers.

0numbers the graph read from it
0cells of the map it votes in
103citing papers in PubMed
10.0field-weighted citation impact, top 1% 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

103 citing papers in PubMed, 169 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article

43 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

28 authors at 9 institutions in 6 countries.

Stéphanie LhomondUniversité de Bordeaux, Bordeaux, France.
Tony AvrilINSERM U1242, "Chemistry, Oncogenesis, Stress, Signaling", Université de Rennes 1, Rennes, France.
Nicolas DejeansUniversité de Bordeaux, Bordeaux, France.
Konstantinos VoutetakisInstitute of Biology, Medicinal Chemistry & Biotechnology, NHRF, Athens, Greece.
Dimitrios DoultsinosINSERM U1242, "Chemistry, Oncogenesis, Stress, Signaling", Université de Rennes 1, Rennes, France.
Mari McMahonINSERM U1242, "Chemistry, Oncogenesis, Stress, Signaling", Université de Rennes 1, Rennes, France.
Raphaël PineauINSERM U1242, "Chemistry, Oncogenesis, Stress, Signaling", Université de Rennes 1, Rennes, France.
Joanna ObaczINSERM U1242, "Chemistry, Oncogenesis, Stress, Signaling", Université de Rennes 1, Rennes, France.
Olga PapadodimaInstitute of Biology, Medicinal Chemistry & Biotechnology, NHRF, Athens, Greece.
Florence JouanINSERM U1242, "Chemistry, Oncogenesis, Stress, Signaling", Université de Rennes 1, Rennes, France.
Heloise BourienINSERM U1242, "Chemistry, Oncogenesis, Stress, Signaling", Université de Rennes 1, Rennes, France.
Marianthi LogothetiInstitute of Biology, Medicinal Chemistry & Biotechnology, NHRF, Athens, Greece.
Gwénaële JégouINSERM U1242, "Chemistry, Oncogenesis, Stress, Signaling", Université de Rennes 1, Rennes, France.
Néstor Pallares-LuponUniversité de Bordeaux, Bordeaux, France.
Kathleen SchmitUniversité de Bordeaux, Bordeaux, France.
Pierre-Jean Le ResteINSERM U1242, "Chemistry, Oncogenesis, Stress, Signaling", Université de Rennes 1, Rennes, France.
Amandine EtcheverryIntegrated Functional Genomics and Biomarkers Team, UMR6290, CNRS, Université de Rennes 1, Rennes, France.
Jean MosserIntegrated Functional Genomics and Biomarkers Team, UMR6290, CNRS, Université de Rennes 1, Rennes, France.
Kim BarrosoINSERM U1242, "Chemistry, Oncogenesis, Stress, Signaling", Université de Rennes 1, Rennes, France.
Elodie VauléonINSERM U1242, "Chemistry, Oncogenesis, Stress, Signaling", Université de Rennes 1, Rennes, France.
Marion MaurelINSERM U1242, "Chemistry, Oncogenesis, Stress, Signaling", Université de Rennes 1, Rennes, France.
Afshin SamaliApoptosis Research Centre, School of Natural Sciences, NUI Galway, Galway, Ireland.ORCID 0000-0002-8610-8375
John B PattersonMedinnovata Inc., Ventura, CA, USA.
Olivier PluquetInstitut Pasteur de Lille, CNRS UMR8161 "Mechanisms of Tumourigenesis and Targeted Therapies", Université de Lille, Lille, France.
Claudio HetzBiomedical Neuroscience Institute, Faculty of Medicine, University of Chile, Santiago, Chile.
Véronique QuillienINSERM U1242, "Chemistry, Oncogenesis, Stress, Signaling", Université de Rennes 1, Rennes, France.
Aristotelis ChatziioannouInstitute of Biology, Medicinal Chemistry & Biotechnology, NHRF, Athens, Greece.
Eric ChevetINSERM U1242, "Chemistry, Oncogenesis, Stress, Signaling", Université de Rennes 1, Rennes, France eric.chevet@inserm.fr.ORCID 0000-0001-5855-4522
Inserm · FRUniversité de Bordeaux · FRCentre National de la Recherche Scientifique · FRKuehne + Nagel (Greece) · GRBuck Institute for Research on Aging · USEduInnovation · USInstitute of Molecular Biology and Biotechnology · BGOllscoil na Gaillimhe – University of Galway · IEUniversity of Thessaly · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Proteostasis imbalance is emerging as a major hallmark of cancer, driving tumor aggressiveness. Evidence suggests that the endoplasmic reticulum (ER), a major site for protein folding and quality control, plays a critical role in cancer development. This concept is valid in glioblastoma multiform (GBM), the most lethal primary brain cancer with no effective treatment. We previously demonstrated that the ER stress sensor IRE1α (referred to as IRE1) contributes to GBM progression, through XBP1 mRNA splicing and regulated IRE1-dependent decay (RIDD) of RNA Here, we first demonstrated IRE1 signaling significance to human GBM and defined specific IRE1-dependent gene expression signatures that were confronted to human GBM transcriptomes. This approach allowed us to demonstrate the antagonistic roles of XBP1 mRNA splicing and RIDD on tumor outcomes, mainly through selective remodeling of the tumor stroma. This study provides the first demonstration of a dual role of IRE1 downstream signaling in cancer and opens a new therapeutic window to abrogate tumor progression.

Indexed as

Brain NeoplasmsCarcinogenesisCell Line, TumorEndoribonucleasesGene Expression Regulation, NeoplasticGlioblastomaHumansModels, BiologicalMutationNeoplasm ProteinsPhenotypeProtein Serine-Threonine KinasesRNA, MessengerRNA SplicingSignal TransductionTumor MicroenvironmentEndoribonucleasesERN1 protein, humanNeoplasm ProteinsProtein Serine-Threonine KinasesRNA, Messengercancerendoplasmic reticulumIRE1regulated IRE1‐dependent decayXBP1

Identifiers

PMID29311133
PMCPMC5840541
OpenAlexW2782992910

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.