Evidence map›Paper›PMID 30718660›Full record

ArticleScientific reports2019

A novel immunogenic mouse model of melanoma for the preclinical assessment of combination targeted and immune-based therapy.

Emily J Lelliott, Carleen Cullinane, Claire A Martin, Rachael Walker, Kelly M Ramsbottom, Fernando Souza-Fonseca-Guimaraes, Shatha Abuhammad, Jessica Michie, Laura Kirby, Richard J Young and 7 more

Open access · goldAbstract 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. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

13 citing papers in PubMed, 28 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

17 authors at 3 institutions in 2 countries.

Emily J LelliottCancer Research Division, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Carleen CullinaneCancer Research Division, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Claire A MartinCancer Research Division, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Rachael WalkerCancer Research Division, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Kelly M RamsbottomCancer Research Division, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Fernando Souza-Fonseca-GuimaraesDepartment of Medical Biology, University of Melbourne, Melbourne, VIC, Australia.
Shatha AbuhammadCancer Research Division, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Jessica MichieCancer Research Division, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Laura KirbyCancer Research Division, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Richard J YoungCancer Research Division, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Alison SlaterCancer Research Division, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Peter LauCancer Research Division, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.ORCID 0000-0003-1071-7956
Katrina MeethDepartment of Pathology, Yale University School of Medicine, New Haven, CT, USA.
Jane OliaroCancer Research Division, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Nicole HaynesCancer Research Division, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Grant A McArthurCancer Research Division, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Karen E SheppardCancer Research Division, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia. karen.sheppard@petermac.org.ORCID 0000-0002-2798-4703
The University of Melbourne · AUPeter MacCallum Cancer Centre · AUYale University · US

Funding

EPA EP-C-15-008
6 · The paper itself

Abstract

Both targeted therapy and immunotherapy have been used successfully to treat melanoma, but the development of resistance and poor response rates to the individual therapies has limited their success. Designing rational combinations of targeted therapy and immunotherapy may overcome these obstacles, but requires assessment in preclinical models with the capacity to respond to both therapeutic classes. Herein, we describe the development and characterization of a novel, immunogenic variant of the Braf

Indexed as

Disease Models, AnimalAnimalsAntineoplastic Agents, ImmunologicalAntineoplastic Combined Chemotherapy ProtocolsCell Line, TumorCostimulatory and Inhibitory T-Cell ReceptorsCyclin-Dependent Kinase Inhibitor p16Drug Screening Assays, AntitumorHumansMaleMAP Kinase Signaling SystemMelanomaMiceMice, TransgenicMitogen-Activated Protein Kinase KinasesOvalbuminAntineoplastic Agents, ImmunologicalBraf protein, mouseCdkn2a protein, mouseCostimulatory and Inhibitory T-Cell ReceptorsCyclin-Dependent Kinase Inhibitor p16Mitogen-Activated Protein Kinase KinasesOvalbuminProtein Kinase InhibitorsProto-Oncogene Proteins B-rafPTEN PhosphohydrolasePten protein, mouse

Identifiers

PMID30718660
PMCPMC6361951
OpenAlexW2921886023

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.