Evidence map›Paper›PMID 19477944›Full record

ReviewEndocrine reviews2009

Unraveling insulin-like growth factor binding protein-3 actions in human disease.

Sherryline Jogie-Brahim, David Feldman, Youngman Oh

Open access · bronzeAbstract readReview
In one paragraph

Review in Endocrine reviews, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 154 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
154citing papers in PubMed, 2 pooled it
14.8field-weighted citation impact, top 1% 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

154 citing papers in PubMed, 2 syntheses or guidelines pooled it, 323 citations in OpenAlex.

  1. Pooled it
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  3. Trial
  4. Trial
  5. Association between IGFBP-3 and longitudinal neuropsychiatric symptom trajectories in early Parkinson's disease: a longitudinal cohort study.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
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94 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Sherryline Jogie-BrahimDepartment of Pathology, Medical College of Virginia Campus, Virginia Commonwealth University, Richmond, Virginia 23298-0662, USA.
David Feldman
Youngman Oh
Virginia Commonwealth University Medical Center · USStanford University · US

Funding

VITAMIN D RECEPTOR AND REGULATION OF HORMONE RESPONSER01DK042482 · NIDDK · STANFORD UNIVERSITY · PI FELDMAN, DAVID · 1991 to 2010
$3.1M
VITAMIN D RECEPTOR AND REGULATION OF HORMONE RESPONSER56DK042482 · NIDDK · STANFORD UNIVERSITY · PI FELDMAN, DAVID · 2005 to 2005
$115k
NIDDK NIH HHS DK42482NIDDK NIH HHS R01 DK042482NIDDK NIH HHS R56 DK042482
6 · The paper itself

Abstract

The IGF system plays critical roles in somatic growth in an endocrine fashion (somatomedin hypothesis) as well as proliferation and differentiation of normal and malignant cells in a paracrine/autocrine fashion. IGFBP-3 is known to modulate the actions of IGFs in circulation as well as the immediate extracellular environment. Interestingly, apart from the ability to inhibit or enhance IGF actions, IGFBP-3 also exhibits very clear, distinct biological effects independent of the IGF/IGF-I receptor axis. Over the past decade it has become widely appreciated that IGF/IGF-IR-independent actions of IGFBP-3 (antiproliferative and proapoptotic effects) contribute to improving the pathophysiology of a variety of human diseases, such as cancer, diabetes, and malnutrition. Recent studies have implicated interaction of IGFBP-3 with a variety of proteins or signaling cascades critical to cell cycle control and apoptosis; however, the actual mechanism of IGFBP-3 action is still unclear. This review reinforces the concept in support of the IGF/IGF-IR axis-independent actions of IGFBP-3 and delineates potential underlying mechanisms involved and subsequent biological significance, focusing in particular on functional binding partners and the clinical significance of IGFBP-3 in the assessment of cancer risk.

Indexed as

Active Transport, Cell NucleusAnimalsCell DifferentiationCell NucleusCell ProliferationConserved SequenceGene ExpressionHumansInsulin-Like Growth Factor Binding Protein 3Insulin-Like Growth Factor Binding ProteinsNeoplasmsPolymorphism, GeneticProtein BindingReceptor, IGF Type 1Receptors, Cell SurfaceRisk FactorsIGFBP3 protein, humanInsulin-Like Growth Factor Binding Protein 3Insulin-Like Growth Factor Binding ProteinsReceptor, IGF Type 1Receptors, Cell SurfaceSomatomedins

Identifiers

PMID19477944
PMCPMC2819737
OpenAlexW2011369409

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.