Evidence map›Paper›PMID 30137431›Full record

ArticleNucleic acids research2018

SOX4 can redirect TGF-β-mediated SMAD3-transcriptional output in a context-dependent manner to promote tumorigenesis.

Stephin J Vervoort, Ana Rita Lourenço, Ana Tufegdzic Vidakovic, Enric Mocholi, José L Sandoval, Oscar M Rueda, Cynthia Frederiks, Cornelieke Pals, Janneke G C Peeters, Carlos Caldas and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
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  10. Review
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  14. Analysis of the DNA-binding properties of TGF-β-activated Smad complexes unveils a possible molecular basis for cellular context-dependent signaling.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  15. Article
  16. SOX on tumors, a comfort or a constraint?Cell death discovery · 2024
    Review
  17. RSK3 switches cell fate: from stress-induced senescence to malignant progression.Journal of experimental & clinical cancer research : CR · 2023
    Article
  18. Inhibition of the lncRNAMolecular therapy. Nucleic acids · 2022
    Article
  19. Article
  20. Article
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

12 authors at 4 institutions in 2 countries.

Stephin J VervoortCenter for Molecular Medicine, University Medical Center Utrecht, Utrecht, The Netherlands.
Ana Rita LourençoCenter for Molecular Medicine, University Medical Center Utrecht, Utrecht, The Netherlands.
Ana Tufegdzic VidakovicMechanisms of Transcription Laboratory, The Francis Crick Institute, London NW1 1AT, UK.
Enric MocholiCenter for Molecular Medicine, University Medical Center Utrecht, Utrecht, The Netherlands.
José L SandovalCancer Research UK Cambridge Institute, and Department of Oncology, Li Ka Shing Centre, University of Cambridge, Cambridge CB2 0RE, UK.
Oscar M RuedaCancer Research UK Cambridge Institute, and Department of Oncology, Li Ka Shing Centre, University of Cambridge, Cambridge CB2 0RE, UK.
Cynthia FrederiksCenter for Molecular Medicine, University Medical Center Utrecht, Utrecht, The Netherlands.
Cornelieke PalsCenter for Molecular Medicine, University Medical Center Utrecht, Utrecht, The Netherlands.
Janneke G C PeetersLaboratory of Translational Immunology, University Medical Center Utrecht, Utrecht University, 3508 AB Utrecht, The Netherlands.
Carlos CaldasCancer Research UK Cambridge Institute, and Department of Oncology, Li Ka Shing Centre, University of Cambridge, Cambridge CB2 0RE, UK.
Alejandra BrunaCancer Research UK Cambridge Institute, and Department of Oncology, Li Ka Shing Centre, University of Cambridge, Cambridge CB2 0RE, UK.
Paul J CofferCenter for Molecular Medicine, University Medical Center Utrecht, Utrecht, The Netherlands.
University Medical Center Utrecht · NLUniversity of Cambridge · GBUtrecht University · NLThe Francis Crick Institute · GB

Funding

Cancer Research UK 16942
6 · The paper itself

Abstract

Expression of the transcription factor SOX4 is often elevated in human cancers, where it generally correlates with tumor-progression and poor-disease outcome. Reduction of SOX4 expression results in both diminished tumor-incidence and metastasis. In breast cancer, TGF-β-mediated induction of SOX4 has been shown to contribute to epithelial-to-mesenchymal transition (EMT), which controls pro-metastatic events. Here, we identify SMAD3 as a novel, functionally relevant SOX4 interaction partner. Genome-wide analysis showed that SOX4 and SMAD3 co-occupy a large number of genomic loci in a cell-type specific manner. Moreover, SOX4 expression was required for TGF-β-mediated induction of a subset of SMAD3/SOX4-co-bound genes regulating migration and extracellular matrix-associated processes, and correlating with poor-prognosis. These findings identify SOX4 as an important SMAD3 co-factor controlling transcription of pro-metastatic genes and context-dependent shaping of the cellular response to TGF-β. Targeted disruption of the interaction between these factors may have the potential to disrupt pro-oncogenic TGF-β signaling, thereby impairing tumorigenesis.

Indexed as

Breast NeoplasmsCarcinogenesisEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticHumansMCF-7 CellsPrognosisSignal TransductionSmad3 ProteinSOXC Transcription FactorsTranscription, GeneticTransforming Growth Factor betaSmad3 ProteinSMAD3 protein, humanSOX4 protein, humanSOXC Transcription FactorsTransforming Growth Factor beta

Identifiers

PMID30137431
PMCPMC6182182
OpenAlexW2888558340

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.