Evidence map›Paper›PMID 21145819›Full record

ArticleJournal of hepatology2011

Overexpression of the IGF2-mRNA binding protein p62 in transgenic mice induces a steatotic phenotype.

Elisabeth Tybl, Fu-Dong Shi, Sonja M Kessler, Sascha Tierling, Jörn Walter, Rainer M Bohle, Stefan Wieland, Jianying Zhang, Eng M Tan, Alexandra K Kiemer

Abstract read
In one paragraph

Article in Journal of hepatology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

35 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. IMPlications of IMP2 in RNA Biology and Disease.International journal of molecular sciences · 2025
    Review
  7. Decoding mGenes & diseases · 2024
    Review
  8. IGF2BPs as novel mGenes & diseases · 2024
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  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

10 authors at 4 institutions in 2 countries.

Elisabeth TyblSaarland University, Department of Pharmacy, Pharmaceutical Biology, Saarbrücken, Germany.
Fu-Dong Shi
Sonja M Kessler
Sascha Tierling
Jörn Walter
Rainer M Bohle
Stefan Wieland
Jianying Zhang
Eng M Tan
Alexandra K Kiemer
Saarland University · DEScripps Research Institute · USBarrow Neurological Institute · USThe University of Texas at El Paso · US

Funding

NK cells in CNS inflammation and autoimmunityR01AI083294 · NIAID · ST. JOSEPH'S HOSPITAL AND MEDICAL CENTER · PI SHI, FU-DONG · 2010 to 2014
$2.0M
AUTOANTIBODIES IN HEPATOCELLULAR CARCINOMAR01CA056956 · NCI · SCRIPPS RESEARCH INSTITUTE · PI TAN, ENG M · 1992 to 2005
$1.9M
NCI NIH HHS CA 56956NCI NIH HHS R01 CA056956NIAID NIH HHS R01 AI083294
6 · The paper itself

Abstract

BACKGROUND &

aimsThe insulin-like growth-factor 2 (IGF2) mRNA binding protein p62 is highly expressed in hepatocellular carcinoma tissue. Still, its potential role in liver disease is largely unknown. In this study, we investigated pathophysiological implications of p62 overexpression in mice.

methodsWe generated mice overexpressing p62 under a LAP-promotor. mRNA expression levels and stability were examined by real-time RT-PCR. Allele-specific expression of Igf2 and H19 was assessed after crossing mice with SD7 animals. The Igf2 downstream mediators pAKT and PTEN were determined by Western blot.

resultsHepatic p62 overexpression neither induced inflammatory processes nor liver damage. However, 2.5week old transgenic animals displayed a steatotic phenotype and improved glucose tolerance. p62 overexpression induced the expression of the imprinted genes Igf2 and H19 and their transcriptional regulator Aire (autoimmune regulator). Neither monoallelic expression nor mRNA stability of Igf2 and H19 was affected. Investigating Igf2 downstream signalling pathways showed increased AKT activation and attenuated PTEN expression.

conclusionsThe induction of a steatotic phenotype implies that p62 plays a role in hepatic pathophysiology.

Indexed as

AnimalsFatty LiverGene ExpressionGlucose IntoleranceHumansInsulin-Like Growth Factor IILiverMiceMice, TransgenicNon-alcoholic Fatty Liver DiseasePhenotypePromoter Regions, GeneticRNA, MessengerTranscription FactorsTranscription Factor TFIIHGtf2h1 protein, mouseIGF2 protein, mouseInsulin-Like Growth Factor IIRNA, MessengerTranscription FactorsTranscription Factor TFIIH

Identifiers

PMID21145819
PMCPMC3079004
OpenAlexW2066542744

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.