Evidence map›Paper›PMID 11716066›Full record

ReviewJournal of neuro-oncology2001

Biological mechanisms of glioma invasion and potential therapeutic targets.

B B Tysnes, R Mahesparan

Abstract readReview
PubMed Publisher
In one paragraph

Review in Journal of neuro-oncology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

48 citing papers in PubMed, 101 citations in OpenAlex.

  1. Article
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  4. AssociatingAJNR. American journal of neuroradiology · 2023
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  17. Review
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  19. Article
  20. Glioblastoma multiforme - an overview.Contemporary oncology (Poznan, Poland) · 2014
    Review
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

2 authors at 1 institution in 1 country.

B B TysnesDepartment of Anatomy and Cell Biology, University of Bergen, Norway. berit.tysnes@pki.uib.no
R Mahesparan
University of Bergen · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The current understanding of glioma biology reveals targets for anti-invasive therapy which include manipulations of extracellular matrix and receptors, growth factors and cytokines, proteases, cytoskeletal components, oncogenes and tumor suppressor genes. A better understanding of the complex regulation and the signalling molecules involved in glioma invasion is still needed in order to design new and effective treatment modalities towards invasive tumor cells. Representative and valid in vitro experimental systems and animal models of gliomas are necessary for the characterization of the invasive phenotype and further development of anti-invasive therapy. In the future, it will probably be important to move from comparative genomic modelling through protein characterization based on advanced proteomic techniques to analyse tissue samples, where the aim for gliomas should be to compare invaded and non-invaded tissue. This will hopefully render promising new therapeutic targets for gliomas.

Indexed as

AnimalsAntineoplastic AgentsAstrocytomaBrain NeoplasmsCell Adhesion MoleculesCell MovementChromosome DeletionChromosomes, Human, Pair 10CytoskeletonDisease ProgressionEndopeptidasesExtracellular MatrixForecastingGene Expression Regulation, NeoplasticGenetic TherapyGlioblastomaAntineoplastic AgentsCell Adhesion MoleculesEndopeptidasesGrowth SubstancesIntegrinsNeoplasm ProteinsPhosphoric Monoester HydrolasesProtease InhibitorsPTEN PhosphohydrolasePTEN protein, humanThromboxane-A SynthaseTumor Suppressor Proteins

Identifiers

PMID11716066
OpenAlexW1587753177

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.