Evidence map›Paper›PMID 24633053›Full record

ArticleScientific reports2014

Cyclic glycine-proline regulates IGF-1 homeostasis by altering the binding of IGFBP-3 to IGF-1.

Jian Guan, Peter Gluckman, Panzao Yang, Geoff Krissansen, Xueying Sun, Yongzhi Zhou, Jingyuan Wen, Gemma Phillips, Paul R Shorten, Chris D McMahon and 6 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

16 citing papers in PubMed, 50 citations in OpenAlex.

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  12. The putative etiology and prevention of autism.Progress in molecular biology and translational science · 2020
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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

16 authors at 3 institutions in 1 country.

Jian Guan1] Liggins Institute, University of Auckland, 85 Park Road, Grafton, Auckland, New Zealand [2] Centre for Brain Research, Faculty of Medicine and Health Sciences, University of Auckland, 85 Park Road, Grafton, Auckland, New Zealand [3] Gravida National Centre for Growth and Development, University of Auckland, Auckland, New Zealand.
Peter Gluckman1] Liggins Institute, University of Auckland, 85 Park Road, Grafton, Auckland, New Zealand [2] Gravida National Centre for Growth and Development, University of Auckland, Auckland, New Zealand.
Panzao Yang1] Liggins Institute, University of Auckland, 85 Park Road, Grafton, Auckland, New Zealand [2] Centre for Brain Research, Faculty of Medicine and Health Sciences, University of Auckland, 85 Park Road, Grafton, Auckland, New Zealand.
Geoff KrissansenDepartment of Molecular Medicine and Pathology, Faculty of Medicine and Health Sciences, University of Auckland, 85 Park Road, Grafton, Auckland, New Zealand.
Xueying SunDepartment of Molecular Medicine and Pathology, Faculty of Medicine and Health Sciences, University of Auckland, 85 Park Road, Grafton, Auckland, New Zealand.
Yongzhi Zhou1] Liggins Institute, University of Auckland, 85 Park Road, Grafton, Auckland, New Zealand [2] School of Pharmacy, Faculty of Medicine and Health Sciences, University of Auckland, 85 Park Road, Grafton, Auckland, New Zealand.
Jingyuan WenSchool of Pharmacy, Faculty of Medicine and Health Sciences, University of Auckland, 85 Park Road, Grafton, Auckland, New Zealand.
Gemma Phillips1] Institute of Natural and Mathematical Sciences, Massey University, Private Bag 102904, Auckland, New Zealand [2] AgResearch Ltd, Ruakura Research Centre, Private Bag 3123, Hamilton 3240, New Zealand.
Paul R Shorten1] Gravida National Centre for Growth and Development, University of Auckland, Auckland, New Zealand [2] AgResearch Ltd, Ruakura Research Centre, Private Bag 3123, Hamilton 3240, New Zealand [3] Riddet Institute, Massey University, Private Bag 11222, Palmerston North 4442, New Zealand.
Chris D McMahon1] Gravida National Centre for Growth and Development, University of Auckland, Auckland, New Zealand [2] AgResearch Ltd, Ruakura Research Centre, Private Bag 3123, Hamilton 3240, New Zealand.
Graeme C Wake1] Gravida National Centre for Growth and Development, University of Auckland, Auckland, New Zealand [2] Institute of Natural and Mathematical Sciences, Massey University, Private Bag 102904, Auckland, New Zealand [3] Riddet Institute, Massey University, Private Bag 11222, Palmerston North 4442, New Zealand.
Wendy H K ChanLiggins Institute, University of Auckland, 85 Park Road, Grafton, Auckland, New Zealand.
Mark F ThomasAgResearch Ltd, Ruakura Research Centre, Private Bag 3123, Hamilton 3240, New Zealand.
April RenLiggins Institute, University of Auckland, 85 Park Road, Grafton, Auckland, New Zealand.
Steve MoonLiggins Institute, University of Auckland, 85 Park Road, Grafton, Auckland, New Zealand.
Dong-Xu LiuLiggins Institute, University of Auckland, 85 Park Road, Grafton, Auckland, New Zealand.
University of Auckland · NZAgResearch · NZMassey University · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The homeostasis of insulin-like growth factor-1 (IGF-1) is essential for metabolism, development and survival. Insufficient IGF-1 is associated with poor recovery from wounds whereas excessive IGF-1 contributes to growth of tumours. We have shown that cyclic glycine-proline (cGP), a metabolite of IGF-1, can normalise IGF-1 function by showing its efficacy in improving the recovery from ischemic brain injury in rats and inhibiting the growth of lymphomic tumours in mice. Further investigation in cell culture suggested that cGP promoted the activity of IGF-1 when it was insufficient, but inhibited the activity of IGF-1 when it was excessive. Mathematical modelling revealed that the efficacy of cGP was a modulated IGF-1 effect via changing the binding of IGF-1 to its binding proteins, which dynamically regulates the balance between bioavailable and non-bioavailable IGF-1. Our data reveal a novel mechanism of auto-regulation of IGF-1, which has physiological and pathophysiological consequences and potential pharmacological utility.

Indexed as

AnimalsAntineoplastic AgentsBrain IschemiaCell LineCorpus StriatumEndothelial CellsGene Expression RegulationGlycineHippocampusHomeostasisInsulin-Like Growth Factor Binding Protein 3Insulin-Like Growth Factor ILymphomaMaleMiceModels, StatisticalAntineoplastic AgentsGlycineinsulin-like growth factor-1, mouseinsulin-like growth factor-1, ratInsulin-Like Growth Factor Binding Protein 3Insulin-Like Growth Factor IPeptides, CyclicProlineProtective Agents

Identifiers

PMID24633053
PMCPMC3955921
OpenAlexW2031996819

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.