Evidence map›Paper›PMID 9693381›Full record

ArticleMolecular biology of the cell1998

Transcriptional regulation of fibroblast growth factor-2 expression in human astrocytes: implications for cell plasticity.

J Moffett, E Kratz, J Myers, E K Stachowiak, R Z Florkiewicz, M K Stachowiak

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 59 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.

J MoffettMolecular and Structural Neurobiology and Gene Therapy Program, Barrow Neurological Institute, Phoenix, Arizona 85013, USA.
E Kratz
J Myers
E K Stachowiak
R Z Florkiewicz
M K Stachowiak
Barrow Neurological Institute · USScripps Research Institute · US

Funding

ANGIOTENSIN REGULATION OF GENE EXPRESSIONR01HL049376 · NHLBI · ST. JOSEPH'S HOSP/MED CTR (PHOENIX) · PI STACHOWIAK, MICHAL · 1993 to 2000
$278k
STUDIES WITH GROWTH HORMONE RELEASING FACTORP01DK018811 · NIDDK · WHITTIER INSTITUTE FOR DIABETES &ENDOC · PI MAHER, PAMELA ANNE · 1986 to 1995
–
NHLBI NIH HHS HL-49376-01A1NHLBI NIH HHS R01 HL049376NIDDK NIH HHS P01 DK018811
6 · The paper itself

Abstract

Induction of the fibroblast growth factor-2 (FGF-2) gene and the consequent accumulation of FGF-2 in the nucleus are operative events in mitotic activation and hypertrophy of human astrocytes. In the brain, these events are associated with cellular degeneration and may reflect release of the FGF-2 gene from cell contact inhibition. We used cultures of human astrocytes to examine whether expression of FGF-2 is also controlled by soluble growth factors. Treatment of subconfluent astrocytes with interleukin-1beta, epidermal or platelet-derived growth factors, 18-kDa FGF-2, or serum or direct stimulation of protein kinase C (PKC) with phorbol 12-myristate 13-acetate or adenylate cyclase with forskolin increased the levels of 18-, 22-, and 24-kDa FGF-2 isoforms and FGF-2 mRNA. Transfection of FGF-2 promoter-luciferase constructs identified a unique -555/-513 bp growth factor-responsive element (GFRE) that confers high basal promoter activity and activation by growth factors to a downstream promoter region. It also identified a separate region (-624/-556 bp) essential for PKC and cAMP stimulation. DNA-protein binding assays indicated that novel cis-acting elements and trans-acting factors mediate activation of the FGF-2 gene. Southwestern analysis identified 40-, 50-, 60-, and 100-kDa GFRE-binding proteins and 165-, 112-, and 90-kDa proteins that interacted with the PKC/cAMP-responsive region. The GFRE and the element essential for PKC and cAMP stimulation overlap with the region that mediates cell contact inhibition of the FGF-2 promoter. The results show a two-stage regulation of the FGF-2 gene: 1) an initial induction by reduced cell contact, and 2) further activation by growth factors or the PKC-signaling pathway. The hierarchic regulation of the FGF-2 gene promoter by cell density and growth factors or PKC reflects a two-stage activation of protein binding to the GFRE and to the PKC/cAMP-responsive region, respectively.

Indexed as

Gene Expression RegulationPromoter Regions, GeneticTranscription, GeneticAstrocytesBase SequenceBinding SitesBrainCell NucleusCells, CulturedColforsinDNA-Binding ProteinsEpidermal Growth FactorFibroblast Growth Factor 2HumansInterleukin-1LuciferasesColforsinDNA-Binding ProteinsEpidermal Growth FactorFibroblast Growth Factor 2Interleukin-1LuciferasesOligodeoxyribonucleotidesOligonucleotides, AntisenseRecombinant Fusion ProteinsTetradecanoylphorbol Acetate

Identifiers

PMID9693381
PMCPMC25481
OpenAlexW2127838140

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.