Evidence map›Paper›PMID 27292772›Full record

ArticleInternational journal of experimental pathology2016

Functional roles of CSPG4/NG2 in chondrosarcoma.

Nuor S M Jamil, Asim Azfer, Harrison Worrell, Donald M Salter

Open access · greenAbstract read
In one paragraph

Article in International journal of experimental pathology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

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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

4 authors at 2 institutions in 1 country.

Nuor S M JamilCentre for Genomic and Experimental Medicine, MRC IGMM, University of Edinburgh, Edinburgh, UK.
Asim AzferCentre for Genomic and Experimental Medicine, MRC IGMM, University of Edinburgh, Edinburgh, UK.
Harrison WorrellCentre for Genomic and Experimental Medicine, MRC IGMM, University of Edinburgh, Edinburgh, UK.
Donald M SalterCentre for Genomic and Experimental Medicine, MRC IGMM, University of Edinburgh, Edinburgh, UK.
Edinburgh Cancer Research · GBMRC Institute of Genetics and Molecular Medicine · GB

Funding

Medical Research Council
6 · The paper itself

Abstract

CSPG4/NG2 is a multifunctional transmembrane protein with limited distribution in adult tissues including articular cartilage. The purpose of this study was to investigate the possible roles of CSPG4/NG2 in chondrosarcomas and to establish whether this molecule may have potential for targeted therapy. Stable knock-down of CSPG4/NG2 in the JJ012 chondrosarcoma cell line by shRNA resulted in decreased cell proliferation and migration as well as a decrease in gene expression of the MMP (matrix metalloproteinase) 3 protease and ADAMTS4 (aggrecanase). Chondrosarcoma cells in which CSPG4/NG2 was knocked down were more sensitive to doxorubicin than wild-type cells. The results indicate that CSPG4/NG2 has roles in regulating chondrosarcoma cell function in relation to growth, spread and resistance to chemotherapy and that anti-CSPG4/NG2 therapies may have potential in the treatment of surgically unresectable chondrosarcoma.

Indexed as

AdultAgedAntineoplastic AgentsBone NeoplasmsCartilage, ArticularCell AdhesionCell DeathCell Line, TumorCell MovementCell ProliferationChondroitin Sulfate Proteoglycan 4Chondroitin Sulfate ProteoglycansChondrosarcomaDocetaxelDoxorubicinDrug Resistance, NeoplasmAntineoplastic AgentsChondroitin Sulfate Proteoglycan 4Chondroitin Sulfate ProteoglycansCSPG4 protein, humanDocetaxelDoxorubicinMembrane ProteinsNeoplasm ProteinsPeptide HydrolasesRNA, Small InterferingTaxoidschondrosarcomaCSPG4NG2therapy

Identifiers

PMID27292772
PMCPMC4926050
OpenAlexW2412416274

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.