Evidence map›Paper›PMID 24980480›Full record

ArticleHuman genomics2014

Novel age-dependent targets in vestibular schwannomas.

Amos Toren, Juergen K Reichardt, Ali Andalibi, Nancy Ya-Hsuan Hsu, Joni Doherty, William Slattery, Ruty Mehrian-Shai

Abstract read
In one paragraph

Article in Human genomics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Amos Toren
Juergen K Reichardt
Ali Andalibi
Nancy Ya-Hsuan Hsu
Joni Doherty
William Slattery
Ruty Mehrian-ShaiInstitute for Genetic Medicine, University of Southern California, Keck School of Medicine, Los Angeles, CA 90089, USA. mehrian@usc.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSchwannomas are the most common neurofibromatosis type 2 (NF2)-associated tumors with significant phenotypic heterogeneity in patients. The most severe subtype has an early and rapid progression and the mild type has a later onset and a less aggressive course. The aim of this study was to elucidate the underlying molecular differences between these groups. We compared the gene expression pattern between patients with early to late age of onset.

resultsA gene signature of 21 genes was constructed to differentiate between early-onset and late-onset patients. We confirmed these results by real-time PCR for SNF1LK2, NGFRAP1L1 (BEX 5), GMNN, and EPHA2.

conclusionGenes identified here may be additional aberrations in merlin-depleted cells that govern the disease onset. A significant number of these genes have been suggested as having a role in carcinogenesis and are used as biomarkers for prognosis in several other cancers. The role of these genes in NF2 carcinogenesis and their potential as biomarkers or drug target are worthwhile exploring.

Indexed as

TranscriptomeAdolescentAdultAgedAge FactorsBiomarkers, TumorChildGene Expression ProfilingHumansMiddle AgedMolecular Targeted TherapyNeurofibromatosis 2Biomarkers, Tumor

Identifiers

PMID24980480
PMCPMC4097955

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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.