Evidence map›Paper›PMID 27098175›Full record

ArticleMedical oncology (Northwood, London, England)2016

Inhibition of glioblastoma cell proliferation, migration and invasion by the proteasome antagonist carfilzomib.

Zammam Areeb, Stanley S Stylli, Thomas M B Ware, Nicole C Harris, Lipi Shukla, Ramin Shayan, Lucia Paradiso, Bo Li, Andrew P Morokoff, Andrew H Kaye and 1 more

Open access · greenAbstract read
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In one paragraph

Article in Medical oncology (Northwood, London, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 24 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

11 authors at 4 institutions in 2 countries.

Zammam AreebDepartment of Surgery, The University of Melbourne, The Royal Melbourne Hospital, Level 5, Clinical Sciences Building, Parkville, VIC, 3050, Australia.
Stanley S StylliDepartment of Surgery, The University of Melbourne, The Royal Melbourne Hospital, Level 5, Clinical Sciences Building, Parkville, VIC, 3050, Australia.
Thomas M B WareDepartment of Surgery, The University of Melbourne, The Royal Melbourne Hospital, Level 5, Clinical Sciences Building, Parkville, VIC, 3050, Australia.
Nicole C HarrisRegenerative Surgery Group, O'Brien Institute Tissue Engineering Centre, Fitzroy, VIC, 3065, Australia.
Lipi ShuklaRegenerative Surgery Group, O'Brien Institute Tissue Engineering Centre, Fitzroy, VIC, 3065, Australia.
Ramin ShayanRegenerative Surgery Group, O'Brien Institute Tissue Engineering Centre, Fitzroy, VIC, 3065, Australia.
Lucia ParadisoDepartment of Surgery, The University of Melbourne, The Royal Melbourne Hospital, Level 5, Clinical Sciences Building, Parkville, VIC, 3050, Australia.
Bo LiPaediatric Neurosurgery, Department of Paediatric Surgery, Qilu Hospital, Shandong University, 107#, Wenhua Xi Road, Jinan, 250012, People's Republic of China.
Andrew P MorokoffDepartment of Surgery, The University of Melbourne, The Royal Melbourne Hospital, Level 5, Clinical Sciences Building, Parkville, VIC, 3050, Australia.
Andrew H KayeDepartment of Surgery, The University of Melbourne, The Royal Melbourne Hospital, Level 5, Clinical Sciences Building, Parkville, VIC, 3050, Australia.
Rodney B LuworDepartment of Surgery, The University of Melbourne, The Royal Melbourne Hospital, Level 5, Clinical Sciences Building, Parkville, VIC, 3050, Australia. rluwor@unimelb.edu.au.
University of Melbourne · AUO'Brien Institute · AUThe Royal Melbourne Hospital · AUQilu Hospital of Shandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma multiforme is the most aggressive and lethal tumor of the central nervous system with limited treatment strategies on offer, and as such the identification of effective novel therapeutic agents is paramount. To examine the efficacy of proteasome inhibitors, we tested bortezomib, carfilzomib, nafamostat mesylate, gabexate mesylate and acetylsalicylic acid on glioblastoma cell viability, migration and invasion. Both bortezomib and carfilzomib produced significant reduction of cell viability, while nafamostat mesylate, gabexate mesylate and acetylsalicylic acid did not. Subsequent testing showed that carfilzomib significantly reduced cell viability at nM concentrations. Carfilzomib also reduced cell migration, secretion and activation of MMP2 and also cell invasion of all four glioblastoma cells tested. In summary, carfilzomib represents a novel, yet FDA-approved agent for the treatment of glioblastoma multiforme.

Indexed as

Antineoplastic AgentsBortezomibBrain NeoplasmsCell Line, TumorCell MovementCell ProliferationDrug Screening Assays, AntitumorGlioblastomaHumansMatrix Metalloproteinase 2OligopeptidesProteasome InhibitorsAntineoplastic AgentsBortezomibcarfilzomibMatrix Metalloproteinase 2MMP2 protein, humanOligopeptidesProteasome InhibitorsCarfilzomibGlioblastoma multiformeInvasionMigrationMMP2Proteasome

Identifiers

PMID27098175
OpenAlexW2341751972

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.