Evidence map›Paper›PMID 19205030›Full record

ArticleHepatology (Baltimore, Md.)2009

Hepatocyte expression of serum response factor is essential for liver function, hepatocyte proliferation and survival, and postnatal body growth in mice.

Kai Sun, Michele A Battle, Ravi P Misra, Stephen A Duncan

Open access · bronzeAbstract read
In one paragraph

Article in Hepatology (Baltimore, Md.), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Cancers · 2021
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. The neuronal activity-driven transcriptome.Molecular neurobiology · 2015
    Review
  12. Article
  13. Serum response factor indirectly regulates type I interferon-signaling in macrophages.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2013
    Article
  14. Article
  15. Serum response factor regulates bone formation via IGF-1 and Runx2 signals.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2012
    Article
  16. Article
  17. Article
  18. Serum response factor: look into the gut.World journal of gastroenterology · 2010
    Review
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.

Kai SunDepartment of Cell Biology, Neurobiology, and Anatomy, Medical College of Wisconsin, Milwaukee, WI 53226, USA.
Michele A Battle
Ravi P Misra
Stephen A Duncan
Medical College of Wisconsin · US

Funding

TRANSCRIPTIONAL REGULAT OF MAMMALIAN HEPATIC DEVELOPMENTR01DK055743 · NIDDK · MEDICAL COLLEGE OF WISCONSIN · PI DUNCAN, STEPHEN A · 2000 to 2014
$4.6M
Transcriptional control of gastrointestinal developmentR01DK066226 · NIDDK · MEDICAL COLLEGE OF WISCONSIN · PI DUNCAN, STEPHEN A · 2004 to 2008
$1.6M
Transcriptional Control of Early Coronary Vascular DevelopmentR01HL084636 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI MISRA, RAVINDRA P · 2007 to 2010
$1.5M
The role of HNF4 in gastrointestinal developmentF32DK067808 · NIDDK · MEDICAL COLLEGE OF WISCONSIN · PI BATTLE, MICHELE A · 2004 to 2006
$137k
NHLBI NIH HHS R01 HL084636NIDDK NIH HHS DK55743NIDDK NIH HHS DK66226NIDDK NIH HHS F32 DK067808NIDDK NIH HHS R01 DK055743NIDDK NIH HHS R01 DK066226
6 · The paper itself

Abstract

unlabelledSerum response factor (SRF) is a transcription factor that binds to a CarG box motif within the serum response element of genes that are expressed in response to mitogens. SRF plays essential roles in muscle and nervous system development; however, little is known about the role of SRF during liver growth and function. To examine the function of SRF in the liver, we generated mice in which the Srf gene was specifically disrupted in hepatocytes. The survival of mice lacking hepatic SRF activity was lower than that of control mice; moreover, surviving mutant mice had lower blood glucose and triglyceride levels compared with control mice. In addition, Srf(loxP/loxP)AlfpCre mice were smaller and had severely depressed levels of serum insulin-like growth factor 1 (IGF-1). Srf-deficient livers were also smaller than control livers, and liver cell proliferation and viability were compromised. Gene array analysis of SRF depleted livers revealed a reduction in many messenger RNAs, including those encoding components of the growth hormone/IGF-1 pathway, cyclins, several metabolic regulators, and cytochrome p450 enzymes.

conclusionSRF is essential for hepatocyte proliferation and survival, liver function, and control of postnatal body growth by regulating hepatocyte gene expression.

Indexed as

Body SizeAnimalsBlood GlucoseCell ProliferationCell SurvivalFemaleGene ExpressionHepatocytesInsulin-Like Growth Factor ILiverMaleMiceMice, KnockoutOrganogenesisOrgan SizeSerum Response FactorBlood Glucoseinsulin-like growth factor-1, mouseInsulin-Like Growth Factor ISerum Response FactorTriglycerides

Identifiers

PMID19205030
PMCPMC2810404
OpenAlexW2128587465

What Socratic 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 Socratic graph.