Evidence map›Paper›PMID 32812257›Full record

ArticleThe EMBO journal2020

Prevention of dsRNA-induced interferon signaling by AGO1x is linked to breast cancer cell proliferation.

Souvik Ghosh, Joao C Guimaraes, Manuela Lanzafame, Alexander Schmidt, Afzal Pasha Syed, Beatrice Dimitriades, Anastasiya Börsch, Shreemoyee Ghosh, Nitish Mittal, Thomas Montavon and 7 more

Open access · hybridAbstract read
In one paragraph

Article in The EMBO journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Response to Suresh et al.The EMBO journal · 2025
    Article
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  6. Review
  7. Article
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  9. Endogenous Retroviral Elements Generate Pathologic Neutrophils in Pulmonary Arterial Hypertension.American journal of respiratory and critical care medicine · 2022
    Article
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  11. Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Stop codon read-through of mammalianThe Journal of biological chemistry · 2020
    Article
  17. Article
  18. Review
  19. 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

17 authors at 4 institutions in 3 countries.

Souvik Ghosh *Computational and Systems Biology, Biozentrum, University of Basel, Basel, Switzerland.ORCID 0000-0003-4152-4460
Joao C Guimaraes *Computational and Systems Biology, Biozentrum, University of Basel, Basel, Switzerland.ORCID 0000-0002-1664-472X
Manuela LanzafameInstitute of Pathology, University Hospital Basel, Basel, Switzerland.
Alexander SchmidtProteomics Core Facility, Biozentrum, University of Basel, Basel, Switzerland.
Afzal Pasha SyedComputational and Systems Biology, Biozentrum, University of Basel, Basel, Switzerland.
Beatrice DimitriadesComputational and Systems Biology, Biozentrum, University of Basel, Basel, Switzerland.
Anastasiya BörschComputational and Systems Biology, Biozentrum, University of Basel, Basel, Switzerland.
Shreemoyee GhoshComputational and Systems Biology, Biozentrum, University of Basel, Basel, Switzerland.ORCID 0000-0002-1843-7791
Nitish MittalComputational and Systems Biology, Biozentrum, University of Basel, Basel, Switzerland.
Thomas MontavonArchitecture et Réactivité de l'ARN, Institut de biologie moléculaire et cellulaire du CNRS, Université de Strasbourg, Strasbourg, France.
Ana Luisa CorreiaDepartment of Biomedicine, University of Basel/University Hospital Basel, Basel, Switzerland.
Johannes DannerDepartment of Biochemistry, Department of Biology and Preclinical Medicine, University of Regensburg, Regensburg, Germany.
Gunter MeisterDepartment of Biochemistry, Department of Biology and Preclinical Medicine, University of Regensburg, Regensburg, Germany.
Luigi M TerraccianoInstitute of Pathology, University Hospital Basel, Basel, Switzerland.
Sébastien PfefferArchitecture et Réactivité de l'ARN, Institut de biologie moléculaire et cellulaire du CNRS, Université de Strasbourg, Strasbourg, France.
Salvatore PiscuoglioInstitute of Pathology, University Hospital Basel, Basel, Switzerland.
Mihaela ZavolanComputational and Systems Biology, Biozentrum, University of Basel, Basel, Switzerland.ORCID 0000-0002-8832-2041
University of Basel · CHCentre National de la Recherche Scientifique · FRUniversity Hospital of Basel · CHUniversity of Regensburg · DE

Funding

Deutsche Forschungsgemeinschaft SFB960EC|FP7|FP7 Ideas: European Research Council (FP7 Ideas) ERC-CoG-647455French National Research Agency ANR-10-LABX-0036_NETRNASchweiz (Swiss Cancer League) KFS-3995-08-2016Schweiz (Swiss Cancer League) KLS-3639-02-2015Swiss National Science Foundation 51NF40_141735Swiss National Science Foundation PZ00P3_168165SystemsX.ch (Swiss SystemsX.ch) 51FSP0_157344University of Basel
6 · The paper itself

Abstract

Translational readthrough, i.e., elongation of polypeptide chains beyond the stop codon, was initially reported for viral RNA, but later found also on eukaryotic transcripts, resulting in proteome diversification and protein-level modulation. Here, we report that AGO1x, an evolutionarily conserved translational readthrough isoform of Argonaute 1, is generated in highly proliferative breast cancer cells, where it curbs accumulation of double-stranded RNAs (dsRNAs) and consequent induction of interferon responses and apoptosis. In contrast to other mammalian Argonaute protein family members with primarily cytoplasmic functions, AGO1x exhibits nuclear localization in the vicinity of nucleoli. We identify AGO1x interaction with the polyribonucleotide nucleotidyltransferase 1 (PNPT1) and show that the depletion of this protein further augments dsRNA accumulation. Our study thus uncovers a novel function of an Argonaute protein in buffering the endogenous dsRNA-induced interferon responses, different than the canonical function of AGO proteins in the miRNA effector pathway. As AGO1x expression is tightly linked to breast cancer cell proliferation, our study thus suggests a new direction for limiting tumor growth.

Indexed as

Argonaute ProteinsBreast NeoplasmsCell ProliferationEukaryotic Initiation FactorsExoribonucleasesFemaleHEK293 CellsHeLa CellsHumansInterferonsMitochondrial ProteinsNeoplasm ProteinsProtein IsoformsRNA, Double-StrandedSignal TransductionAGO1 protein, humanArgonaute ProteinsEukaryotic Initiation FactorsExoribonucleasesInterferonsMitochondrial ProteinsNeoplasm ProteinsPNPT1 protein, humanProtein IsoformsRNA, Double-StrandedArgonaute 1breast cancerendogenous dsRNAinterferon responsetranslation readthrough

Identifiers

PMID32812257
PMCPMC7507497
OpenAlexW3070115663

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.