Evidence map›Paper›PMID 21506108›Full record

ArticleJournal of cellular physiology2011

Induction of Id-1 by FGF-2 involves activity of EGR-1 and sensitizes neuroblastoma cells to cell death.

Giovanni Passiatore, Antonio Gentilella, Slava Rom, Marco Pacifici, Valeria Bergonzini, Francesca Peruzzi

Abstract read
In one paragraph

Article in Journal of cellular physiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

18 citing papers in PubMed, 26 citations in OpenAlex.

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  7. Heparin-binding epidermal growth factor-like growth factor promotes neuroblastoma differentiation.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2017
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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 4 institutions in 2 countries.

Giovanni PassiatoreDepartment of Neurology and Neuroscience, Weill Cornell Medical College, New York, New York, USA.
Antonio Gentilella
Slava Rom
Marco Pacifici
Valeria Bergonzini
Francesca Peruzzi
Louisiana State University Health Sciences Center New Orleans · USTemple University · USCornell University · USUniversity of Padua · IT

Funding

Mechanisms involved in HIV-1 Tat mediated neuronal damageR01MH079751 · NIMH · TEMPLE UNIV OF THE COMMONWEALTH · PI PERUZZI, FRANCESCA · 2007 to 2011
$1.5M
NIMH NIH HHS MH079751NIMH NIH HHS R01 MH079751
6 · The paper itself

Abstract

Inhibitor of differentiation-1 (Id-1) is a member of helix-loop-helix (HLH) family of proteins that regulate gene transcription through their inhibitory binding to basic-HLH transcription factors. Similarly to other members of this family, Id-1 is involved in the repression of cell differentiation and activation of cell growth. The dual function of Id-1, inhibition of differentiation, and stimulation of cell proliferation, might be interdependent, as cell differentiation is generally coupled with the exit from the cell cycle. Fibroblast growth factor-2 (FGF-2) has been reported to play multiple roles in different biological processes during development of the central nervous system (CNS). In addition, FGF-2 has been described to induce "neuronal-like" differentiation and trigger apoptosis in neuroblastoma SK-N-MC cells. Although regulation of Id-1 protein by several mitogenic factors is well-established, little is known about the role of FGF-2 in the regulation of Id-1. Using human neuroblastoma cell line, SK-N-MC, we found that treatment of these cells with FGF-2 resulted in early induction of both Id-1 mRNA and protein. The induction occurs within 1 h from FGF-2 treatment and is mediated by ERK1/2 pathway, which in turn stimulates expression of the early growth response-1 (Egr-1) transcription factor. We also demonstrate direct interaction of Egr-1 with Id-1 promoter in vitro and in cell culture. Finally, inhibition of Id-1 expression results in G(2) /M accumulation of FGF-2-treated cells and delayed cell death.

Indexed as

ApoptosisBinding SitesBrain NeoplasmsCell CycleCell Line, TumorEarly Growth Response Protein 1Fibroblast Growth Factor 2Gene Expression Regulation, NeoplasticHumansInhibitor of Differentiation Protein 1Mitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3NeuroblastomaPromoter Regions, GeneticRecombinant ProteinsRNA InterferenceEarly Growth Response Protein 1EGR1 protein, humanFibroblast Growth Factor 2ID1 protein, humanInhibitor of Differentiation Protein 1MAPK1 protein, humanMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Recombinant ProteinsRNA, Messenger

Identifiers

PMID21506108
PMCPMC3760689
OpenAlexW2028871894

What OpenQuestion holds

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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.