Evidence map›Paper›PMID 24067366›Full record

ReviewCell cycle (Georgetown, Tex.)2013

Identifying new small molecule anti-invasive compounds for glioma treatment.

Jennifer Munson, Michael Bonner, Levi Fried, Jonathan Hofmekler, Jack Arbiser, Ravi Bellamkonda

Abstract readReview
In one paragraph

Review in Cell cycle (Georgetown, Tex.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
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

21 citing papers in PubMed.

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  14. VEGF-B-Neuropilin-1 signaling is spatiotemporally indispensable for vascular and neuronal development in zebrafish.Proceedings of the National Academy of Sciences of the United States of America · 2015
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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.

Jennifer MunsonWallace H. Coulter Department of Biomedical Engineering; Georgia Institute of Technology; Atlanta, GA, USA.
Michael Bonner
Levi Fried
Jonathan Hofmekler
Jack Arbiser
Ravi Bellamkonda

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma is a disease with poor survival rates after diagnosis. Treatment of the disease involves debulking of the tumor, which is limited by the degree of invasiveness of the disease. Therefore, a treatment to halt the invasion of glioma is desirable for clinical implementation. There have been several candidate compounds targeting specific aspects of invasion, including cell adhesions, matrix degradation, and cytoskeletal rearrangement, but they have failed clinically for a variety of reasons. New targets against glioma invasion include upstream mediators of these classical targets in an effort to better inhibit invasion with more specificity for cancer. Included in these treatments is a new class of compounds inhibiting the generation of reactive oxygen species by targeting the NADPH oxidases. These compounds stand to inhibit multiple pathways, including nuclear factor kappa B and Akt. By conducting a screen of compounds thought to inhibit these pathways, a new compound to halt invasion was found that may have a beneficial effect against glioma, based on recent publications. Further, there are still limitations to the treatment of glioblastoma regardless of the discovery of new targets and compounds that should be addressed to better the therapies against this deadly cancer.

Indexed as

Drug DiscoveryAntineoplastic AgentsBrain NeoplasmsCell AdhesionCell MovementGlioblastomaHumansMolecular Targeted TherapyNADPH OxidasesNeoplasm InvasivenessNF-kappa BProto-Oncogene Proteins c-aktReactive Oxygen SpeciesSmall Molecule LibrariesAntineoplastic AgentsNADPH OxidasesNF-kappa BProto-Oncogene Proteins c-aktReactive Oxygen SpeciesSmall Molecule Librariescancerdrug screengliomainvasionNADPH oxidase

Identifiers

PMID24067366
PMCPMC3755070

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.