Evidence map›Paper›PMID 30894629›Full record

ArticleScientific reports2019

A reference collection of patient-derived cell line and xenograft models of proneural, classical and mesenchymal glioblastoma.

Brett W Stringer, Bryan W Day, Rochelle C J D'Souza, Paul R Jamieson, Kathleen S Ensbey, Zara C Bruce, Yi Chieh Lim, Kate Goasdoué, Carolin Offenhäuser, Seçkin Akgül and 12 more

Erratum issuedAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 153 papers.

0numbers the graph read from it
0cells of the map it votes in
153citing 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

153 citing papers in PubMed.

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93 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors.

Brett W StringerQIMR Berghofer Medical Research Institute, Brisbane, Australia. brett.w.stringer@gmail.com.ORCID 0000-0003-4552-9736
Bryan W DayQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Rochelle C J D'SouzaQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Paul R JamiesonQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Kathleen S EnsbeyQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Zara C BruceQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Yi Chieh LimQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Kate GoasdouéQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Carolin OffenhäuserQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Seçkin AkgülQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Suzanne AllanQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Thomas RobertsonRoyal Brisbane and Women's Hospital, Brisbane, Australia.
Peter LucasRoyal Brisbane and Women's Hospital, Brisbane, Australia.
Gert TollessonRoyal Brisbane and Women's Hospital, Brisbane, Australia.
Scott CampbellRoyal Brisbane and Women's Hospital, Brisbane, Australia.
Craig WinterRoyal Brisbane and Women's Hospital, Brisbane, Australia.
Hongdo DoOlivia Newton-John Cancer and Wellness Centre, Melbourne, Australia.
Alexander DobrovicOlivia Newton-John Cancer and Wellness Centre, Melbourne, Australia.ORCID 0000-0003-3414-112X
Po-Ling InglisQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Rosalind L JeffreeRoyal Brisbane and Women's Hospital, Brisbane, Australia.
Terrance G JohnsHudson Institute of Medical Research, Clayton, Victoria, Australia.
Andrew W BoydQIMR Berghofer Medical Research Institute, Brisbane, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Low-passage, serum-free cell lines cultured from patient tumour tissue are the gold-standard for preclinical studies and cellular investigations of glioblastoma (GBM) biology, yet entrenched, poorly-representative cell line models are still widely used, compromising the significance of much GBM research. We submit that greater adoption of these critical resources will be promoted by the provision of a suitably-sized, meaningfully-described reference collection along with appropriate tools for working with them. Consequently, we present a curated panel of 12 readily-usable, genetically-diverse, tumourigenic, patient-derived, low-passage, serum-free cell lines representing the spectrum of molecular subtypes of IDH-wildtype GBM along with their detailed phenotypic characterisation plus a bespoke set of lentiviral plasmids for bioluminescent/fluorescent labelling, gene expression and CRISPR/Cas9-mediated gene inactivation. The cell lines and all accompanying data are readily-accessible via a single website, Q-Cell (qimrberghofer.edu.au/q-cell/) and all plasmids are available from Addgene. These resources should prove valuable to investigators seeking readily-usable, well-characterised, clinically-relevant, gold-standard models of GBM.

Indexed as

Cell Line, TumorNeoplasm TransplantationAgedAged, 80 and overAnimalsBrain NeoplasmsFemaleGlioblastomaHumansMaleMice, Inbred NODMice, SCIDMiddle Aged

Identifiers

PMID30894629
PMCPMC6427001

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.