Evidence map›Paper›PMID 20655258›Full record

ArticleGrowth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society2010

Identification of differentially expressed genes in the kidneys of growth hormone transgenic mice.

K T Coschigano, A N Wetzel, N Obichere, A Sharma, S Lee, R Rasch, M M Guigneaux, A Flyvbjerg, T G Wood, J J Kopchick

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In one paragraph

Article in Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.6field-weighted citation impact, top 27% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
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  8. Article
  9. GH and IGF1: roles in energy metabolism of long-living GH mutant mice.The journals of gerontology. Series A, Biological sciences and medical sciences · 2012
    Review
  10. Article
  11. Growth hormone, inflammation and aging.Pathobiology of aging & age related diseases · 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

10 authors at 4 institutions in 2 countries.

K T CoschiganoDepartment of Biomedical Sciences, College of Osteopathic Medicine, 228 Irvine Hall, Ohio University, Athens, OH 45701, USA. coschigk@ohio.edu
A N Wetzel
N Obichere
A Sharma
S Lee
R Rasch
M M Guigneaux
A Flyvbjerg
T G Wood
J J Kopchick
Ohio University · USAarhus University Hospital · DKThe University of Texas Medical Branch at Galveston · USBiotechnology Institute · US

Funding

The Somatotropic Axis and Health Aging: A Search for MechanismsP01AG031736 · NIA · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI KIRKLAND, JAMES L. · 2009 to 2013
$8.4M
Longevity genes and calorie restriction: early post-natal effectsR01AG019899 · NIA · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI BARTKE, ANDRZEJ · 2001 to 2016
$6.1M
Cross-talk between growth hormone and inflammation pathways in kidney damageR15DK081192 · NIDDK · OHIO UNIVERSITY ATHENS · PI COSCHIGANO, KAREN T · 2008 to 2010
$272k
Creation and characterization of GH binding protein gene disrupted miceR15DK075436 · NIDDK · OHIO UNIVERSITY ATHENS · PI KOPCHICK, JOHN J · 2007 to 2007
$221k
Role of KAP expression in the diabetic kidneyR15DK061952 · NIDDK · OHIO UNIVERSITY ATHENS · PI COSCHIGANO, KAREN T · 2002 to 2002
$145k
NIA NIH HHS P01 AG031736NIA NIH HHS P01 AG031736-01A1NIA NIH HHS R01 AG019899NIA NIH HHS R01 AG19899-05NIDDK NIH HHS 1 R15 DK061952-01NIDDK NIH HHS 1 R15 DK081192-01NIDDK NIH HHS R15 DK061952NIDDK NIH HHS R15 DK075436NIDDK NIH HHS R15DK075436NIDDK NIH HHS R15 DK081192
6 · The paper itself

Abstract

objectiveBovine growth hormone (bGH) transgenic mice develop severe kidney damage. This damage may be due, at least in part, to changes in gene expression. Identification of genes with altered expression in the bGH kidney may identify mechanisms leading to damage in this system that may also be relevant to other models of kidney damage.

designcDNA subtraction libraries, northern blot analyses, microarray analyses and real-time reverse transcription polymerase chain reaction (RT/PCR) assays were used to identify and verify specific genes exhibiting differential RNA expression between kidneys of bGH mice and their non-transgenic (NT) littermates.

resultsImmunoglobulins were the vast majority of genes identified by the cDNA subtractions and the microarray analyses as being up-regulated in bGH. Several glycoprotein genes and inflammation-related genes also showed increased RNA expression in the bGH kidney. In contrast, only a few genes were identified as being significantly down-regulated in the bGH kidney. The most notable decrease in RNA expression was for the gene encoding kidney androgen-regulated protein.

conclusionsA number of genes were identified as being differentially expressed in the bGH kidney. Inclusion of two groups, immunoglobulins and inflammation-related genes, suggests a role of the immune system in bGH kidney damage.

Indexed as

Gene ExpressionAnimalsCattleDown-RegulationFemaleGene Expression ProfilingGlycoproteinsGrowth HormoneImmunityImmunoglobulinsKidneyKidney DiseasesMiceMice, Inbred C57BLMice, TransgenicUp-RegulationGlycoproteinsGrowth Hormonegrowth hormone, bovineImmunoglobulins

Identifiers

PMID20655258
PMCPMC2948615
OpenAlexW2039585880

What OpenQuestion holds

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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.