Evidence map›Paper›PMID 24658685›Full record

ArticleNature cell biology2014

A time- and matrix-dependent TGFBR3-JUND-KRT5 regulatory circuit in single breast epithelial cells and basal-like premalignancies.

Chun-Chao Wang, Sameer S Bajikar, Leen Jamal, Kristen A Atkins, Kevin A Janes

Abstract read
In one paragraph

Article in Nature cell biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing 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

55 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Ribosomal Protein S6: A Potential Therapeutic Target against Cancer?International journal of molecular sciences · 2021
    Review
  13. Review
  14. Article
  15. Post-transcriptional tuning of FGF signaling mediates neural crest induction.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  16. β-Catenin signaling dynamics regulate cell fate in differentiating neural stem cells.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  17. Article
  18. miR-206 family is important for mitochondrial and muscle function, but not essential for myogenesis in vitro.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Chun-Chao WangDepartment of Biomedical Engineering, University of Virginia, Charlottesville Virginia 22908, USA.
Sameer S BajikarDepartment of Biomedical Engineering, University of Virginia, Charlottesville Virginia 22908, USA.
Leen Jamal1] Department of Biomedical Engineering, University of Virginia, Charlottesville Virginia 22908, USA [2].
Kristen A AtkinsDepartment of Pathology, University of Virginia, Charlottesville Virginia 22908, USA.
Kevin A JanesDepartment of Biomedical Engineering, University of Virginia, Charlottesville Virginia 22908, USA.

Funding

Women's Oncology Program - WONP30CA044579 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Thomas P. Loughran · 1987 to 2026
$72.1M
Stochastic Control of Abnormal Morphogenesis Induced by the ErbB2 OncoproteinDP2OD006464 · OD · UNIVERSITY OF VIRGINIA · PI JANES, KEVIN A · 2009 to 2009
$2.3M
NCI NIH HHS P30 CA044579NIH HHS 1-P2-OD006464NIH HHS DP2 OD006464
6 · The paper itself

Abstract

Basal-like breast carcinoma is characterized by poor prognosis and high intratumour heterogeneity. In an immortalized basal-like breast epithelial cell line, we identified two anticorrelated gene-expression programs that arise among single extracellular matrix (ECM)-attached cells during organotypic three-dimensional culture. The first contains multiple TGF-β-related genes including TGFBR3, whereas the second contains JUND and the basal-like marker KRT5. TGFBR3 and JUND interconnect through four negative-feedback loops to form a circuit that exhibits spontaneous damped oscillations in three-dimensional culture. The TGFBR3-JUND circuit is conserved in some premalignant lesions that heterogeneously express KRT5. The circuit depends on ECM engagement, as detachment causes a rewiring that is triggered by RPS6 dephosphorylation and maintained by juxtacrine tenascin C, which is critical for intraductal colonization of basal-like breast cancer cells in vivo. Intratumour heterogeneity need not stem from partial differentiation and could instead reflect dynamic toggling of cells between expression states that are not cell autonomous.

Indexed as

AnimalsBreast NeoplasmsCarcinoma, Intraductal, NoninfiltratingCell DifferentiationCell Line, TumorEpithelial CellsExtracellular MatrixFemaleHumansKeratin-5MiceMice, SCIDPhosphorylationProteoglycansProto-Oncogene Proteins c-junReceptors, Transforming Growth Factor betabetaglycanJunD protein, humanKeratin-5KRT5 protein, humanProteoglycansProto-Oncogene Proteins c-junReceptors, Transforming Growth Factor betaRibosomal Protein S6RNA, Small InterferingTenascin

Identifiers

PMID24658685
PMCPMC4035356

What OpenQuestion holds

Textmetadata
LicenceTDM
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.