Evidence map›Paper›PMID 12612091›Full record

ArticleMolecular and cellular biology2003

Brain lipid binding protein in axon-Schwann cell interactions and peripheral nerve tumorigenesis.

Shyra J Miller, Hongzhen Li, Tilat A Rizvi, Yuan Huang, Gunnar Johansson, Jason Bowersock, Amer Sidani, John Vitullo, Kristine Vogel, Linda M Parysek and 2 more

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
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  7. β-1,4-Galactosyltransferase-involved in lipopolysaccharide-induced adhesion of Schwann cells.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2011
    Article
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  16. Mechanisms and roles of axon-Schwann cell interactions.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2004
    Review
  17. Article
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

12 authors at 2 institutions in 1 country.

Shyra J MillerDepartment of Cell Biology, Neurobiology and Anatomy, University of Cincinnati College of Medicine, 231 Bethesda Avenue, Cincinnati, OH 45267-0521, USA.
Hongzhen Li
Tilat A Rizvi
Yuan Huang
Gunnar Johansson
Jason Bowersock
Amer Sidani
John Vitullo
Kristine Vogel
Linda M Parysek
Jeffrey E DeClue
Nancy Ratner
University of Cincinnati Medical Center · USNational Cancer Institute · US

Funding

MITOGENIC ACTIVITIES IN NEUROFIBROMATOSISR01NS028840 · NINDS · UNIVERSITY OF CINCINNATI · PI NANCY RATNER · 1990 to 2026
$10.1M
NINDS NIH HHS NS 28840NINDS NIH HHS R01 NS028840
6 · The paper itself

Abstract

Loss of axonal contact characterizes Schwann cells in benign and malignant peripheral nerve sheath tumors (MPNST) from neurofibromatosis type 1 (NF1) patients. Tumor Schwann cells demonstrate NF1 mutations, elevated Ras activity, and aberrant epidermal growth factor receptor (EGFR) expression. Using cDNA microarrays, we found that brain lipid binding protein (BLBP) is elevated in an EGFR-positive subpopulation of Nf1 mutant mouse Schwann cells (Nf1(-/-) TXF) that grows away from axons; BLBP expression was not affected by farnesyltransferase inhibitor, an inhibitor of H-Ras. BLBP was also detected in EGFR-positive cell lines derived from Nf1:p53 double mutant mice and human MPNST. BLBP expression was induced in normal Schwann cells following transfection with EGFR but not H-Ras12V. Furthermore, EGFR-mediated BLBP expression was not inhibited by dominant-negative H-Ras, indicating that BLBP expression is downstream of Ras-independent EGFR signaling. BLBP-blocking antibodies enabled process outgrowth from Nf1(-/-) TXF cells and restored interaction with axons, without affecting cell proliferation or migration. Following injury, BLBP expression was induced in normal sciatic nerves when nonmyelinating Schwann cells remodeled their processes. These data suggest that BLBP, stimulated by Ras-independent pathways, regulates Schwann cell-axon interactions in normal peripheral nerve and peripheral nerve tumors.

Indexed as

Tumor Suppressor ProteinsAnimalsAxonsCarrier ProteinsCell MovementCells, CulturedCytoplasmErbB ReceptorsFatty Acid-Binding Protein 7Fatty Acid-Binding ProteinsGene Expression ProfilingGene Expression Regulation, NeoplasticGenes, DominantGenes, Neurofibromatosis 1Genes, rasHumansCarrier ProteinsErbB ReceptorsFABP7 protein, humanFabp7 protein, mouseFatty Acid-Binding Protein 7Fatty Acid-Binding ProteinsMembrane ProteinsNeoplasm ProteinsNerve Tissue ProteinsNeurofibromin 1Recombinant Fusion ProteinsRNA, MessengerRNA, NeoplasmTumor Suppressor Proteins

Identifiers

PMID12612091
PMCPMC149461
OpenAlexW2166298884

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.