Evidence map›Paper›PMID 26458334›Full record

ArticleScientific reports2015

Junb controls lymphatic vascular development in zebrafish via miR-182.

Kristin Kiesow, Katrin Bennewitz, Laura Gutierrez Miranda, Sandra J Stoll, Bettina Hartenstein, Peter Angel, Jens Kroll, Marina Schorpp-Kistner

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.1field-weighted citation impact, top 19% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Lymphatic vasculature in ovarian cancer.Biochimica et biophysica acta. Reviews on cancer · 2023
    Review
  6. Role of miRNAs in vascular development.Non-coding RNA research · 2023
    Review
  7. Role of miR-182 in cardiovascular and cerebrovascular diseases.Frontiers in cell and developmental biology · 2023
    Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Genetic compensation byCell cycle (Georgetown, Tex.) · 2019
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Erratum.Investigative ophthalmology & visual science · 2016
    Article
  19. 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

8 authors at 4 institutions in 1 country.

Kristin KiesowDivision of Signal Transduction and Growth Control, DKFZ-ZMBH Alliance, German Cancer Research Center (DKFZ), Heidelberg, D-69120, Germany.
Katrin BennewitzDepartment of Vascular Biology and Tumor Angiogenesis, Center for Biomedicine and Medical Technology Mannheim (CBTM), Medical Faculty Mannheim, Heidelberg University, Mannheim, D-68167, Germany.
Laura Gutierrez MirandaDivision of Signal Transduction and Growth Control, DKFZ-ZMBH Alliance, German Cancer Research Center (DKFZ), Heidelberg, D-69120, Germany.
Sandra J StollDepartment of Vascular Biology and Tumor Angiogenesis, Center for Biomedicine and Medical Technology Mannheim (CBTM), Medical Faculty Mannheim, Heidelberg University, Mannheim, D-68167, Germany.
Bettina HartensteinDivision of Signal Transduction and Growth Control, DKFZ-ZMBH Alliance, German Cancer Research Center (DKFZ), Heidelberg, D-69120, Germany.
Peter AngelDivision of Signal Transduction and Growth Control, DKFZ-ZMBH Alliance, German Cancer Research Center (DKFZ), Heidelberg, D-69120, Germany.
Jens KrollDepartment of Vascular Biology and Tumor Angiogenesis, Center for Biomedicine and Medical Technology Mannheim (CBTM), Medical Faculty Mannheim, Heidelberg University, Mannheim, D-68167, Germany.
Marina Schorpp-KistnerDivision of Signal Transduction and Growth Control, DKFZ-ZMBH Alliance, German Cancer Research Center (DKFZ), Heidelberg, D-69120, Germany.
DKFZ-ZMBH Alliance · DEUniversity Hospital Heidelberg · DEGerman Cancer Research Center · DEHeidelberg University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

JUNB, a subunit of the AP-1 transcription factor complex, mediates gene regulation in response to a plethora of extracellular stimuli. Previously, JUNB was shown to act as a critical positive regulator of blood vessel development and homeostasis as well as a negative regulator of proliferation, inflammation and tumour growth. Here, we demonstrate that the oncogenic miR-182 is a novel JUNB target. Loss-of-function studies by morpholino-mediated knockdown and the CRISPR/Cas9 technology identify a novel function for both JUNB and its target miR-182 in lymphatic vascular development in zebrafish. Furthermore, we show that miR-182 attenuates foxo1 expression indicating that strictly balanced Foxo1 levels are required for proper lymphatic vascular development in zebrafish. In conclusion, our findings uncover with the Junb/miR-182/Foxo1 regulatory axis a novel key player in governing lymphatic vascular morphogenesis in zebrafish.

Indexed as

Gene Expression RegulationLymphangiogenesisAnimalsEctopic Gene ExpressionForkhead Box Protein O1Forkhead Transcription FactorsGene Knockdown TechniquesGene SilencingMicroRNAsPhenotypeProto-Oncogene Proteins c-junThoracic DuctZebrafishZebrafish ProteinsForkhead Box Protein O1Forkhead Transcription Factorsfoxo1a protein, zebrafishMicroRNAsProto-Oncogene Proteins c-junZebrafish Proteins

Identifiers

PMID26458334
PMCPMC4602192
OpenAlexW2403296790

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LicenceCC BY
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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.