Evidence map›Paper›PMID 21703424›Full record

ArticleThe American journal of pathology2011

NPAS3 demonstrates features of a tumor suppressive role in driving the progression of Astrocytomas.

Frederico Moreira, Tim-Rasmus Kiehl, Kelvin So, Norbert F Ajeawung, Carmelita Honculada, Peter Gould, Russell O Pieper, Deepak Kamnasaran

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

22 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
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  6. Frontiers in cellular neuroscience · 2022
    Article
  7. Review
  8. Homologue-specific chromosome sequencing characterizes translocation junctions and permits allelic assignment.DNA research : an international journal for rapid publication of reports on genes and genomes · 2018
    Article
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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

8 authors at 7 institutions in 4 countries.

Frederico MoreiraCentre de Recherche de l'Hôtel-Dieu de Québec, Québec, Québec, Canada.
Tim-Rasmus Kiehl
Kelvin So
Norbert F Ajeawung
Carmelita Honculada
Peter Gould
Russell O Pieper
Deepak Kamnasaran
University Health Network · CADulbecco Telethon Institute · ITHôpital de l'Enfant-Jésus · CAHôtel-Dieu de Québec · CAThe Priory Hospital · GBUniversité Laval · CAUniversity of California, San Francisco · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malignant astrocytomas, the most common primary brain tumors, are predominantly fatal. Improved treatments will require a better understanding of the biological features of high-grade astrocytomas. To better understand the role of neuronal PAS 3 (NPAS3) in diseases in human beings, it was investigated as a candidate for astrocytomagenesis based on the presence of aberrant protein expression in greater than 70% of a human astrocytoma panel (n = 433) and most notably in surgically resected malignant lesions. In subsequent functional studies, it was concluded that NPAS3 exhibits features of a tumor-suppressor, which drives the progression of astrocytomas by modulating the cell cycle, proliferation, apoptosis, and cell migration/invasion and has a further influence on the viability of endothelial cells. Of clinical importance, absence of NPAS3 expression in glioblastomas was a significantly negative prognostic marker of survival. In addition, malignant astrocytomas lacking NPAS3 expression demonstrated loss of function mutations, which were associated with loss of heterozygosity. While overexpressed NPAS3 in malignant glioma cell lines significantly suppressed transformation, the converse decreased expression considerably induced more aggressive growth. In addition, knockdown NPAS3 expression in a human astrocyte cell line in concert with the human papillomavirus E6 and E7 oncogenes induced growth of malignant astrocytomas. In conclusion, NPAS3 drives the progression of human malignant astrocytomas as a tumor suppressor and is a negative prognostication marker for survival.

Indexed as

Cell Transformation, NeoplasticAnimalsApoptosisAstrocytomaBasic Helix-Loop-Helix ProteinsBlotting, WesternBrainBrain NeoplasmsCell AdhesionCell CycleCell MovementCell ProliferationCells, CulturedDNA MethylationEndothelium, VascularFluorescent Antibody TechniqueBasic Helix-Loop-Helix ProteinsNerve Tissue ProteinsNPAS3 protein, humanRNA, MessengerTranscription FactorsTumor Suppressor Proteins

Identifiers

PMID21703424
PMCPMC3123785
OpenAlexW2053356709

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.