Evidence map›Paper›PMID 21865067›Full record

ArticleGrowth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society2011

The effects of type 1 IGF receptor inhibition in a mouse model of diabetic kidney disease.

Ariel Troib, Daniel Landau, Jack F Youngren, Leonid Kachko, Ralph Rabkin, Yael Segev

Abstract read
In one paragraph

Article in Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 86% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

6 authors at 3 institutions in 2 countries.

Ariel TroibShraga Segal Department of Microbiology and Immunology, Ben Gurion University of the Negev, Beer Sheva, Israel.
Daniel Landau
Jack F Youngren
Leonid Kachko
Ralph Rabkin
Yael Segev
Ben-Gurion University of the Negev · ILStanford University · USUniversity of California, San Francisco · US

Funding

DAUs as IGF-1 Receptor Inhibitors in Breast CancerR01CA112042 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI YOUNGREN, JACK F · 2007 to 2010
$1.2M
Skeletal Muscle Growth Hormone Resistance In UremiaR01DK068517 · NIDDK · STANFORD UNIVERSITY · PI RABKIN, RALPH · 2006 to 2008
$605k
NCI NIH HHS R01 CA112042NIDDK NIH HHS R01 DK 068517NIDDK NIH HHS R01 DK068517
6 · The paper itself

Abstract

objectiveWe have recently shown increased sensitivity to IGF-I induced signal transduction in kidneys of diabetic mice. Accordingly we investigated the effects of PQ401, a novel diarylurea compound that inhibits IGF1R autophosphorylation in type I diabetes.

methodsControl (C) and Diabetic (D) mice were administered PQ401 (CP, DP) or vehicle (C, D) for 3weeks.

resultsCP animals showed a decrease in renal phosphorylated (p-)AKT and p-IGF1R. However, PQ401 had no effect on diabetic state (hyperglycemia, weight loss) or renal disease parameters (hypertrophy, hyperfiltration and albuminuria). Type IV collagen as well as TGF-β mRNA increased in DP and D compared to C. In the CP group renal hypertrophy with fat accumulation in proximal tubuli and increased renal IGF-I, collagen IV and TGF-β mRNA were seen.

conclusionsIGF1R inhibition by PQ401 exerted no significant effects on diabetic kidney disease parameters, arguing against a role for IGF-I in the pathogenesis of diabetic kidney disease. However, PQ401 affects normal kidneys, inducing renal hypertrophy as well as collagen and fat accumulation, with increased renal IGF-I mRNA, suggestive of a damage-regeneration process. Therefore, this diarylurea compound is not beneficial in early diabetic kidney disease. Its potential deleterious effects on kidney tissue need to be further investigated.

Indexed as

AminoquinolinesAnimalsCollagen Type IVDiabetes Mellitus, ExperimentalDiabetic NephropathiesDisease Models, AnimalGene Expression RegulationInsulin-Like Growth Factor IMiceMice, Inbred NODPhenylurea CompoundsPhosphorylationReceptor, IGF Type 1Transforming Growth Factor beta1AminoquinolinesCollagen Type IVInsulin-Like Growth Factor IPhenylurea CompoundsPQ 401Receptor, IGF Type 1Transforming Growth Factor beta1

Identifiers

PMID21865067
PMCPMC4238882
OpenAlexW2078390966

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.