Evidence map›Paper›PMID 31068593›Full record

ArticleNature communications2019

Ribosome biogenesis during cell cycle arrest fuels EMT in development and disease.

Varsha Prakash, Brittany B Carson, Jennifer M Feenstra, Randall A Dass, Petra Sekyrova, Ayuko Hoshino, Julian Petersen, Yuan Guo, Matthew M Parks, Chad M Kurylo and 18 more

Abstract 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 158 papers.

0numbers the graph read from it
0cells of the map it votes in
158citing papers in PubMed
–field-weighted citation impact
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

158 citing papers in PubMed.

  1. Article
  2. Deciphering the impact ofGenes & diseases · 2026
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  15. Ribosome Homeostasis Regulated by SETD2 Preserves Intestinal Epithelial Barrier.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

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

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

28 authors.

Varsha PrakashDepartment of Physiology and Pharmacology, Karolinska Institutet, 171 77, Stockholm, Sweden.
Brittany B CarsonDepartment of Physiology and Pharmacology, Karolinska Institutet, 171 77, Stockholm, Sweden.
Jennifer M FeenstraDepartment of Physiology and Pharmacology, Karolinska Institutet, 171 77, Stockholm, Sweden.
Randall A DassDepartment of Physiology and Biophysics, Weill Cornell Medicine, New York, NY, 10065, USA.
Petra SekyrovaDepartment of Immunology, Genetics and Pathology, Uppsala University, 751 85, Uppsala, Sweden.
Ayuko HoshinoMeyer Cancer Center, Weill Cornell Medicine, New York, NY, 10065, USA.
Julian PetersenDepartment of Physiology and Pharmacology, Karolinska Institutet, 171 77, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-7444-0610
Yuan GuoDepartment of Molecular Biosciences, The Wenner-Gren Institute, Stockholm University, S-10691, Stockholm, Sweden.
Matthew M ParksDepartment of Physiology and Biophysics, Weill Cornell Medicine, New York, NY, 10065, USA.
Chad M KuryloDepartment of Physiology and Biophysics, Weill Cornell Medicine, New York, NY, 10065, USA.
Jake E BatchelderDepartment of Physiology and Biophysics, Weill Cornell Medicine, New York, NY, 10065, USA.
Kristian HallerDepartment of Laboratory Medicine, Center for Molecular Pathology, Lund University, Lund, SE-223 81, Sweden.
Ayako HashimotoMeyer Cancer Center, Weill Cornell Medicine, New York, NY, 10065, USA.
Helene RundqivstDepartment of Cell and Molecular Biology, Karolinska Institute, Stockholm, SE-171 77, Sweden.ORCID http://orcid.org/0000-0002-5617-9076
John S CondeelisGruss Lipper Biophotonics Center, Albert Einstein College of Medicine, Bronx, 10461, NY, USA.ORCID http://orcid.org/0000-0001-8826-2336
C David AllisLaboratory of Chromatin Biology and Epigenetics, The Rockefeller University, New York, NY, 10065, USA.
Denis DryginPimera, Inc, 3210 Merryfield Row, San Diego, CA, 92121, USA.
M Angela NietoInstituto de Neurociencias, CSIC-UMH, Alicante, 03550, Spain.ORCID http://orcid.org/0000-0002-3538-840X
Michael AndängDepartment of Immunology, Genetics and Pathology, Uppsala University, 751 85, Uppsala, Sweden.ORCID http://orcid.org/0000-0002-2886-7891
Piergiorgio PercipalleScience Division, Biology Program, New York University Abu Dhabi, Abu Dhabi, 129188, UAE.
Jonas BerghDepartment of Oncology and Pathology, Karolinska Institutet and University Hospital, S-171 76, Solna, Sweden.
Igor AdameykoDepartment of Physiology and Pharmacology, Karolinska Institutet, 171 77, Stockholm, Sweden.
Ann-Kristin Östlund FarrantsDepartment of Molecular Biosciences, The Wenner-Gren Institute, Stockholm University, S-10691, Stockholm, Sweden.
Johan HartmanDepartment of Oncology and Pathology, Karolinska Institutet and University Hospital, S-171 76, Solna, Sweden.ORCID http://orcid.org/0000-0002-6500-8527
David LydenMeyer Cancer Center, Weill Cornell Medicine, New York, NY, 10065, USA.ORCID http://orcid.org/0000-0003-0193-4131
Kristian PietrasDepartment of Laboratory Medicine, Center for Molecular Pathology, Lund University, Lund, SE-223 81, Sweden.ORCID http://orcid.org/0000-0001-6738-4705
Scott C BlanchardDepartment of Physiology and Biophysics, Weill Cornell Medicine, New York, NY, 10065, USA. scb2005@med.cornell.edu.ORCID http://orcid.org/0000-0003-2717-9365
C Theresa VincentDepartment of Physiology and Pharmacology, Karolinska Institutet, 171 77, Stockholm, Sweden. theresa.vincent@igp.uu.se.

Funding

Imaging Protein Synthesis on the Ribosome using Single-Molecule FRETR01GM079238 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI BLANCHARD, SCOTT C · 2006 to 2023
$7.0M
NIGMS NIH HHS R01 GM079238
6 · The paper itself

Abstract

Ribosome biogenesis is a canonical hallmark of cell growth and proliferation. Here we show that execution of Epithelial-to-Mesenchymal Transition (EMT), a migratory cellular program associated with development and tumor metastasis, is fueled by upregulation of ribosome biogenesis during G1/S arrest. This unexpected EMT feature is independent of species and initiating signal, and is accompanied by release of the repressive nucleolar chromatin remodeling complex (NoRC) from rDNA, together with recruitment of the EMT-driving transcription factor Snai1 (Snail1), RNA Polymerase I (Pol I) and the Upstream Binding Factor (UBF). EMT-associated ribosome biogenesis is also coincident with increased nucleolar recruitment of Rictor, an essential component of the EMT-promoting mammalian target of rapamycin complex 2 (mTORC2). Inhibition of rRNA synthesis in vivo differentiates primary tumors to a benign, Estrogen Receptor-alpha (ERα) positive, Rictor-negative phenotype and reduces metastasis. These findings implicate the EMT-associated ribosome biogenesis program with cellular plasticity, de-differentiation, cancer progression and metastatic disease.

Indexed as

Gene Expression Regulation, DevelopmentalGene Expression Regulation, NeoplasticAnimalsBreast NeoplasmsCell DifferentiationCell Line, TumorCell MovementCell NucleolusChick EmbryoChromosomal Proteins, Non-HistoneDisease Models, AnimalDNA, RibosomalEpithelial-Mesenchymal TransitionFemaleG1 Phase Cell Cycle CheckpointsGene Expression ProfilingChromosomal Proteins, Non-HistoneDNA, RibosomalRNA, Ribosomal

Identifiers

PMID31068593
PMCPMC6506521

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Registered trials

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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.