Evidence map›Paper›PMID 20976841›Full record

ArticleWorld journal of gastroenterology2010

Daily genetic profiling indicates JAK/STAT signaling promotes early hepatic stellate cell transdifferentiation.

Ashley M Lakner, Cathy C Moore, Alyssa A Gulledge, Laura W Schrum

Open access · hybridAbstract read
In one paragraph

Article in World journal of gastroenterology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

23 citing papers in PubMed, 49 citations in OpenAlex.

  1. Trial
  2. SLIT2 as a key regulator and therapeutic target in liver injury.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
  3. Deciphering the Role of Oroxylin A in Liver Fibrosis.Drug design, development and therapy · 2025
    Review
  4. Modulation of hepatic stellate cells by MutaflorJournal of translational medicine · 2022
    Article
  5. Article
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  9. Article
  10. [Reversal of liver fibrosis through AG490 inhibitor-mediated inhibition of the TGFbeta1-STAT3 pathway].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2015
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Cytokines and STATs in Liver Fibrosis.Frontiers in physiology · 2012
    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

4 authors at 1 institution in 1 country.

Ashley M LaknerDepartment of Biology, University of North Carolina at Charlotte, Charlotte, NC 28223, USA.
Cathy C Moore
Alyssa A Gulledge
Laura W Schrum
University of North Carolina at Charlotte · US

Funding

NFkB-mediated collagen regulation by SAMe in HSCsR01AA014891 · NIAAA · UNIVERSITY OF NORTH CAROLINA CHARLOTTE · PI SCHRUM, LAURA W · 2005 to 2008
$838k
NIAAA NIH HHS R01 AA014891
6 · The paper itself

Abstract

aimTo identify signaling pathways and genes that initiate and commit hepatic stellate cells (HSCs) to transdifferentiation.

methodsPrimary HSCs were isolated from male Sprague-Dawley rats and cultured on plastic for 0-10 d. Gene expression was assessed daily (quiescent to day 10 culture-activation) by real time polymerase chain reaction and data clustered using AMADA software. The significance of JAK/STAT signaling to HSC transdifferentiation was determined by treating cells with a JAK2 inhibitor.

resultsGenetic cluster analyses, based on expression of these 21 genes, showed similar expression profiles on days 1-3, days 5 and 6, and days 7-10, while freshly isolated cells (day Q) and day 4 cells were genotypically distinct from any of the other days. Additionally, gene expression clustering revealed strong upregulation of interleukin-6, JAK2 and STAT3 mRNA in the early stages of activation. Inhibition of the JAK/STAT signaling pathway impeded the morphological transdifferentiation of HSCs which correlated with decreased mRNA expression of several profibrotic genes including collagens, α-SMA, PDGFR and TGFβR.

conclusionThese data demonstrate unique clustered genetic profiles during the daily progression of HSC transdifferentiation and that JAK/STAT signaling may be critical in the early stages of transdifferentiation.

Indexed as

Gene Expression ProfilingActinsAnimalsCells, CulturedCell TransdifferentiationCollagenHepatic Stellate CellsInterleukin-6Janus Kinase 2MaleModels, AnimalRatsRats, Sprague-DawleyReceptors, Platelet-Derived Growth FactorReceptors, Transforming Growth Factor betaSignal TransductionActa2 protein, ratActinsCollagenInterleukin-6Jak2 protein, ratJanus Kinase 2Receptors, Platelet-Derived Growth FactorReceptors, Transforming Growth Factor betaStat3 protein, ratSTAT3 Transcription Factor

Identifiers

PMID20976841
PMCPMC2965281
OpenAlexW2069643978

What OpenQuestion holds

Textmetadata
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.