Evidence map›Paper›PMID 31089132›Full record

ArticleNature communications2019

Nucleoporin Nup155 is part of the p53 network in liver cancer.

Kerstin Holzer, Alessandro Ori, Amy Cooke, Daniel Dauch, Elisabeth Drucker, Philip Riemenschneider, Amparo Andres-Pons, Amanda L DiGuilio, Marie-Therese Mackmull, Jochen Baßler and 9 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

29 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
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  8. Postexercise downregulation ofTranslational cancer research · 2024
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  9. Article
  10. Nuclear mRNA export.Acta biochimica et biophysica Sinica · 2024
    Review
  11. Advances in the understanding of nuclear pore complexes in human diseases.Journal of cancer research and clinical oncology · 2024
    Review
  12. Review
  13. Article
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  15. Article
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  19. Review
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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

19 authors at 8 institutions in 3 countries.

Kerstin HolzerInstitute of Pathology, University Hospital Heidelberg, 69120, Heidelberg, Germany.
Alessandro OriLeibniz-Institute on Aging, Fritz-Lipmann-Institute (FLI), 07745, Jena, Germany.
Amy CookeEuropean Molecular Biology Laboratory, Directors' Research Unit, 69117, Heidelberg, Germany.
Daniel DauchDepartment of Internal Medicine VIII, University Hospital Tuebingen, 72076, Tuebingen, Germany.
Elisabeth DruckerInstitute of Pathology, University Hospital Heidelberg, 69120, Heidelberg, Germany.
Philip RiemenschneiderInstitute of Pathology, University Medicine Greifswald, 17475, Greifswald, Germany.
Amparo Andres-PonsEuropean Molecular Biology Laboratory, Structural and Computational Biology Unit, 69117, Heidelberg, Germany.
Amanda L DiGuilioDepartment of Chemistry, Chemical Biology and Biomedical Engineering, Stevens Institute of Technology, Hoboken, NJ, 07030, USA.
Marie-Therese MackmullEuropean Molecular Biology Laboratory, Structural and Computational Biology Unit, 69117, Heidelberg, Germany.
Jochen BaßlerHeidelberg University Biochemistry Center, 69120, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-7441-7867
Stephanie RoesslerInstitute of Pathology, University Hospital Heidelberg, 69120, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-5333-5942
Kai BreuhahnInstitute of Pathology, University Hospital Heidelberg, 69120, Heidelberg, Germany.
Lars ZenderDepartment of Internal Medicine VIII, University Hospital Tuebingen, 72076, Tuebingen, Germany.
Joseph S GlavyDepartment of Chemistry, Chemical Biology and Biomedical Engineering, Stevens Institute of Technology, Hoboken, NJ, 07030, USA.
Frank DombrowskiInstitute of Pathology, University Medicine Greifswald, 17475, Greifswald, Germany.
Ed HurtHeidelberg University Biochemistry Center, 69120, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-4535-8255
Peter SchirmacherInstitute of Pathology, University Hospital Heidelberg, 69120, Heidelberg, Germany.
Martin BeckEuropean Molecular Biology Laboratory, Structural and Computational Biology Unit, 69117, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-7397-1321
Stephan SingerInstitute of Pathology, University Hospital Heidelberg, 69120, Heidelberg, Germany. stephan.singer@uni-greifswald.de.
Heidelberg University · DEEuropean Molecular Biology Laboratory · DEGerman Cancer Research Center · DEStevens Institute of Technology · USUniversitätsmedizin Greifswald · DEEuropean Molecular Biology Laboratory · DELeibniz Institute on Aging - Fritz Lipmann Institute (FLI) · DEMax Planck Institute of Biophysics · DE

Funding

Regulation of Pore Membrane Proteins during NPC Release and Dispersal in Open MitosisR15GM119118 · NIGMS · UNIVERSITY OF TEXAS TYLER · PI GLAVY, JOSEPH STEPHEN · 2016 to 2016
$394k
Deutsche Forschungsgemeinschaft (German Research Foundation) Si1487/3-1Deutsche Forschungsgemeinschaft (German Research Foundation) TRR/SF209 (B04)NIGMS NIH HHS R15 GM119118
6 · The paper itself

Abstract

Cancer-relevant signalling pathways rely on bidirectional nucleocytoplasmic transport events through the nuclear pore complex (NPC). However, mechanisms by which individual NPC components (Nups) participate in the regulation of these pathways remain poorly understood. We discover by integrating large scale proteomics, polysome fractionation and a focused RNAi approach that Nup155 controls mRNA translation of p21 (CDKN1A), a key mediator of the p53 response. The underlying mechanism involves transcriptional regulation of the putative tRNA and rRNA methyltransferase FTSJ1 by Nup155. Furthermore, we observe that Nup155 and FTSJ1 are p53 repression targets and accordingly find a correlation between the p53 status, Nup155 and FTSJ1 expression in murine and human hepatocellular carcinoma. Our data suggest an unanticipated regulatory network linking translational control by and repression of a structural NPC component modulating the p53 pathway through its effectors.

Indexed as

AnimalsCarcinoma, HepatocellularCell Line, TumorCyclin-Dependent Kinase Inhibitor p21Datasets as TopicGene Expression Regulation, NeoplasticHumansLiver NeoplasmsLiver Neoplasms, ExperimentalMethyltransferasesMiceNuclear Pore Complex ProteinsNuclear ProteinsRNA, Small InterferingTumor Suppressor Protein p53CDKN1A protein, humanCyclin-Dependent Kinase Inhibitor p21FTSJ1 protein, humanMethyltransferasesNuclear Pore Complex ProteinsNuclear ProteinsNUP155 protein, humanNUP155 protein, mouseRNA, Small InterferingTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID31089132
PMCPMC6517424
OpenAlexW2945729240

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.