Evidence map›Paper›PMID 25944618›Full record

ArticleOncotarget2015

OVOL guides the epithelial-hybrid-mesenchymal transition.

Dongya Jia, Mohit Kumar Jolly, Marcelo Boareto, Princy Parsana, Steven M Mooney, Kenneth J Pienta, Herbert Levine, Eshel Ben-Jacob

Abstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing 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

76 citing papers in PubMed.

  1. Review
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  4. Article
  5. Review
  6. Article
  7. Article
  8. IgA nephropathy.Nature reviews. Disease primers · 2023
    Review
  9. Review
  10. Theoretical and computational tools to model multistable gene regulatory networks.Reports on progress in physics. Physical Society (Great Britain) · 2023
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Biomedicines · 2021
    Article

16 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

8 authors.

Dongya JiaCenter for Theoretical Biological Physics, Rice University, Houston, TX 77005, USA.
Mohit Kumar JollyCenter for Theoretical Biological Physics, Rice University, Houston, TX 77005, USA.
Marcelo BoaretoCenter for Theoretical Biological Physics, Rice University, Houston, TX 77005, USA.
Princy ParsanaDepartment of Computer Science, Johns Hopkins University, Baltimore, MD 21287, USA.
Steven M MooneyThe James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
Kenneth J PientaThe James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
Herbert LevineCenter for Theoretical Biological Physics, Rice University, Houston, TX 77005, USA.
Eshel Ben-JacobCenter for Theoretical Biological Physics, Rice University, Houston, TX 77005, USA.

Funding

Tumor microvesicle-mediated modulation of the bone microenvironmentP01CA093900 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PIENTA, KENNETH J. · 2004 to 2024
$29.6M
TRANS_NETWORK PROJECTSU54CA143803 · NCI · PRINCETON UNIVERSITY · PI GETZENBERG, ROBERT H. · 2009 to 2013
$14.2M
Mechanisms That Regulate Dormancy of Disseminated Tumor Cells in the Bone MarrowU54CA163124 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SHIOZAWA, YUSUKE · 2011 to 2015
$3.0M
Reactive Stroma and Tumor Associated Macrophages in Prostate Cancer ProgressionU01CA143055 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PIENTA, KENNETH J., ROWLEY, DAVID R · 2010 to 2014
$2.7M
NCI NIH HHS CA093900NCI NIH HHS CA143055NCI NIH HHS CA163124NCI NIH HHS P01 CA093900NCI NIH HHS U01 CA143055NCI NIH HHS U54 CA143803NCI NIH HHS U54CA143803NCI NIH HHS U54 CA163124
6 · The paper itself

Abstract

Metastasis involves multiple cycles of Epithelial-to-Mesenchymal Transition (EMT) and its reverse-MET. Cells can also undergo partial transitions to attain a hybrid epithelial/mesenchymal (E/M) phenotype that has maximum cellular plasticity and allows migration of Circulating Tumor Cells (CTCs) as a cluster. Hence, deciphering the molecular players helping to maintain the hybrid E/M phenotype may inform anti-metastasis strategies. Here, we devised a mechanism-based mathematical model to couple the transcription factor OVOL with the core EMT regulatory network miR-200/ZEB that acts as a three-way switch between the E, E/M and M phenotypes. We show that OVOL can modulate cellular plasticity in multiple ways - restricting EMT, driving MET, expanding the existence of the hybrid E/M phenotype and turning both EMT and MET into two-step processes. Our theoretical framework explains the differences between the observed effects of OVOL in breast and prostate cancer, and provides a platform for investigating additional signals during metastasis.

Indexed as

DNA-Binding ProteinsEpithelial-Mesenchymal TransitionHomeodomain ProteinsHumansMaleMicroRNAsModels, TheoreticalNeoplasm MetastasisProstatic NeoplasmsSystems BiologyTranscription FactorsZinc Finger E-box-Binding Homeobox 1DNA-Binding ProteinsHomeodomain ProteinsMicroRNAsMIRN200 microRNA, humanOVOL1 protein, humanTranscription FactorsZEB1 protein, humanZinc Finger E-box-Binding Homeobox 1cancer systems biologyEMTmetastasisOVOLpartial EMT

Identifiers

PMID25944618
PMCPMC4558162

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.