Evidence map›Paper›PMID 18160678›Full record

ArticleBiology of reproduction2008

Glial cell missing 1 regulates placental growth factor (PGF) gene transcription in human trophoblast.

Miao Chang, Debashree Mukherjea, Ryan M Gobble, Kathleen A Groesch, Ronald J Torry, Donald S Torry

Open access · bronzeAbstract read
In one paragraph

Article in Biology of reproduction, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

34 citing papers in PubMed, 67 citations in OpenAlex.

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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

6 authors at 2 institutions in 1 country.

Miao ChangDepartment of Medical Microbiology, Immunology and Cell Biology, Southern Illinois University School of Medicine, Springfield, Illinois 62794, USA.
Debashree Mukherjea
Ryan M Gobble
Kathleen A Groesch
Ronald J Torry
Donald S Torry
Southern Illinois University School of Medicine · USDrake University · US

Funding

MOLECULAR REGULATION AND ROLE OF PLACENTA GROWTH FACTORR01HD036830 · NICHD · UNIVERSITY OF TENNESSEE KNOXVILLE · PI TORRY, DONALD S. · 1999 to 2010
$1.7M
Expression and function of PIGF in cardiomyocytesR15HL072802 · NHLBI · DRAKE UNIVERSITY · PI TORRY, RONALD J · 2003 to 2003
$144k
NHLBI NIH HHS HL72802NHLBI NIH HHS R15 HL072802NICHD NIH HHS NIH 5R01HD36830NICHD NIH HHS R01 HD036830
6 · The paper itself

Abstract

Placental growth factor (PGF, previously known as PlGF) is prominently expressed by trophoblasts in human placenta, whereas most nontrophoblast cells express low levels of PGF mRNA under normal physiological conditions. We have shown that hypoxia decreases PGF expression in the trophoblast, but little is known about transcriptional regulation of PGF gene expression. We sought to determine promoter regions of the human PGF gene that contribute to its restricted high constitutive expression in the trophoblast. Overlapping putative promoter regions of human PGF gene encompassing 2-1.5 kb were cloned into reporter vectors and co-transfected into trophoblast and nontrophoblast cell lines. Promoter activity generated by a 2-1.5-kb clone was significantly higher in trophoblasts than in nontrophoblasts. Selective deletion mutants showed that a clone encompassing the PGF (2-828/++34) region generated promoter activity similar to the 2-1.5-kb region in the trophoblast. However, deletion of another 131 bp from this subclone (2-698/++34) resulted in significantly less promoter activity in the trophoblast. The (2-828/2-698) region significantly enhanced activity of a minimal promoter construct in trophoblast but not in nontrophoblast cells, suggesting that this region contributes to regulating PGF transcription in the trophoblast. Site-directed mutagenesis of a glial cell missing 1 (GCM1) motif in the 131-bp region significantly decreased enhancer activity in the trophoblast. Furthermore, overexpression of GCM1 significantly increased PGF 2-1.5-kb promoter activity and PGF mRNA expression in trophoblast and nontrophoblast cells. Forced overexpression of GCM1 restored PGF expression in the hypoxic trophoblast. These data support a functional role for GCM1 contributing to constitutively high trophoblast PGF expression and is the first direct evidence of an oxygen-responsive, trophoblast-specific transcription factor contributing to the regulation of PGF expression.

Indexed as

Cell LineCell Line, TumorDNA-Binding ProteinsGene DeletionGene Expression RegulationGenes, ReporterHumansMutationNuclear ProteinsPlacenta Growth FactorPregnancy ProteinsPromoter Regions, GeneticTranscription FactorsTranscription, GeneticTransfectionTrophoblastsDNA-Binding ProteinsGCM1 protein, humanNuclear ProteinsPGF protein, humanPlacenta Growth FactorPregnancy ProteinsTranscription Factors

Identifiers

PMID18160678
PMCPMC2442461
OpenAlexW2154269171

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.