Evidence map›Paper›PMID 32744097›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2020

Hyperphosphorylation of fetal liver IGFBP-1 precedes slowing of fetal growth in nutrient-restricted baboons and may be a mechanism underlying IUGR.

Jenica H Kakadia, Bhawani B Jain, Kyle Biggar, Austen Sutherland, Karen Nygard, Cun Li, Peter W Nathanielsz, Thomas Jansson, Madhulika B Gupta

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Endocrinology and metabolism, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 11 citations in OpenAlex.

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  5. Associations between IGFBP1 gene polymorphisms and the risk of preeclampsia and fetal growth restriction.Hypertension research : official journal of the Japanese Society of Hypertension · 2023
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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

9 authors at 5 institutions in 2 countries.

Jenica H KakadiaDepartment of Biochemistry, University of Western Ontario, London, Ontario, Canada.
Bhawani B JainDepartment of Biochemistry, University of Western Ontario, London, Ontario, Canada.
Kyle BiggarInstitute of Biochemistry, Carleton University, Ottawa, Ontario, Canada.
Austen SutherlandDepartment of Biochemistry, University of Western Ontario, London, Ontario, Canada.
Karen NygardBiotron Integrated Microscopy Facility, University of Western Ontario, London, Ontario, Canada.
Cun LiUniversity of Wyoming, Laramie, Wyoming.
Peter W NathanielszUniversity of Wyoming, Laramie, Wyoming.
Thomas JanssonDivision of Reproductive Sciences, Department of Obstetrics and Gynecology, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
Madhulika B GuptaDepartment of Biochemistry, University of Western Ontario, London, Ontario, Canada.
Western University · CACarleton University · CATexas Biomedical Research Institute · USUniversity of Colorado Anschutz Medical Campus · USUniversity of Wyoming · US

Funding

The Southwest National Primate Research Center Supplement- Infrastructure improvements of ABSL2 holding areasP51OD011133 · OD · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI Larry S. Schlesinger · 2012 to 2026
$129.7M
PARTURITION AND FETAL PRIMATE HYPOTHALAMIC FUNCTIONP01HD021350 · NICHD · UNIVERSITY OF WYOMING · PI JANSSON, THOMAS · 1987 to 2018
$19.9M
IGFBP-1 hyperphosphorylation in IUGR: Role of mTOR and CK2R03HD078313 · NICHD · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI GUPTA, MADHULIKA, JANSSON, THOMAS · 2014 to 2015
$147k
Regulation of IGFBP-1 Phosphorylation in Fetal DevelopmentR03HD093950 · NICHD · UNIVERSITY OF COLORADO DENVER · PI GUPTA, MADHULIKA, JANSSON, THOMAS · 2018 to 2019
$144k
NICHD NIH HHS P01 HD021350NICHD NIH HHS R03 HD078313NICHD NIH HHS R03 HD093950NIH HHS P01HD021350NIH HHS P51 OD011133NIH HHS R03HD078313NIH HHS R03HD093950
6 · The paper itself

Abstract

In cultured fetal liver cells, insulin-like growth factor (IGF) binding protein (IGFBP)-1 hyperphosphorylation in response to hypoxia and amino acid deprivation is mediated by inhibition of mechanistic target of rapamycin (mTOR) and activation of amino acid response (AAR) signaling and casein kinase (CK)2. We hypothesized that fetal liver mTOR inhibition, activation of AAR and CK2, and IGFBP-1 hyperphosphorylation occur before development of intrauterine growth restriction (IUGR). Pregnant baboons were fed a control (C) or a maternal nutrient restriction (MNR; 70% calories of control) diet starting at gestational day (GD) 30 (term GD 185). Umbilical blood and fetal liver tissue were obtained at GD 120 (C,

Indexed as

Fetal DevelopmentPapioAmino AcidsAnimalsCasein Kinase IIFemaleFetal Growth RetardationFood DeprivationGestational AgeInsulin-Like Growth Factor Binding Protein 1LiverOrgan SizePhosphorylationPlacentaPregnancyTOR Serine-Threonine KinasesAmino AcidsCasein Kinase IIInsulin-Like Growth Factor Binding Protein 1TOR Serine-Threonine Kinasescasein kinase IIfetal insulin-like growth factor IprimatesTOR serine-threonine kinases

Identifiers

PMID32744097
PMCPMC7642856
OpenAlexW3047047793

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.