Evidence map›Paper›PMID 27406741›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2016

Defining human insulin-like growth factor I gene regulation.

Aditi Mukherjee, Damir Alzhanov, Peter Rotwein

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Endocrinology and metabolism, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed, 25 citations in OpenAlex.

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  13. Regulation of gene expression by growth hormone.Molecular and cellular endocrinology · 2020
    Review
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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

3 authors at 1 institution in 1 country.

Aditi MukherjeeDepartment of Biochemistry and Molecular Biology, Oregon Health and Science University, Portland, Oregon; and.
Damir AlzhanovDepartment of Biochemistry and Molecular Biology, Oregon Health and Science University, Portland, Oregon; and.
Peter RotweinDepartment of Biochemistry and Molecular Biology, Oregon Health and Science University, Portland, Oregon; and Department of Biomedical Sciences, Paul L. Foster School of Medicine, Texas Tech Health University Health Sciences Center, El Paso, Texas peter.rotwein@ttuhsc.edu.
Oregon Health & Science University · US

Funding

Control of IGF-1 Gene Transcription by Growth HormoneR01DK069703 · NIDDK · OREGON HEALTH & SCIENCE UNIVERSITY · PI ROTWEIN, PETER S · 2006 to 2014
$2.8M
NIDDK NIH HHS R01 DK069703
6 · The paper itself

Abstract

Growth hormone (GH) plays an essential role in controlling somatic growth and in regulating multiple physiological processes in humans and other species. Insulin-like growth factor I (IGF-I), a conserved, secreted 70-amino acid peptide, is a critical mediator of many of the biological effects of GH. Previous studies have demonstrated that GH rapidly and potently promotes IGF-I gene expression in rodents and in some other mammals through the transcription factor STAT5b, leading to accumulation of IGF-I mRNAs and production of IGF-I. Despite this progress, very little is known about how GH or other trophic factors control human IGF1 gene expression, in large part because of the absence of any cellular model systems that robustly express IGF-I. Here, we have addressed mechanisms of regulation of human IGF-I by GH after generating cells in which the IGF1 chromosomal locus has been incorporated into a mouse cell line. Using this model, we found that physiological levels of GH rapidly stimulate human IGF1 gene transcription and identify several potential transcriptional enhancers in chromatin that bind STAT5b in a GH-regulated way. Each of the putative enhancers also activates a human IGF1 gene promoter in reconstitution experiments in the presence of the GH receptor, STAT5b, and GH. Thus we have developed a novel experimental platform that now may be used to determine how human IGF1 gene expression is controlled under different physiological and pathological conditions.

Indexed as

AnimalsCell LineGene Expression RegulationGrowth HormoneHumansInsulin-Like Growth Factor IMiceMice, TransgenicPromoter Regions, GeneticReceptors, SomatotropinReverse Transcriptase Polymerase Chain ReactionRNA, MessengerSTAT5 Transcription FactorTranscription, GeneticGrowth HormoneIGF1 protein, humanInsulin-Like Growth Factor IReceptors, SomatotropinRNA, MessengerSTAT5 Transcription Factorchromatin immunoprecipitationepigeneticsgene transcriptiongrowth hormoneinsulin-like growth factor Isignal transducer and activator of transcription 5b

Identifiers

PMID27406741
PMCPMC5005972
OpenAlexW2474570676

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.