Evidence map›Paper›PMID 25544599›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2015

Mutated BRAF Emerges as a Major Effector of Recurrence in a Murine Melanoma Model After Treatment With Immunomodulatory Agents.

Shane Zaidi, Miran Blanchard, Kevin Shim, Elizabeth Ilett, Karishma Rajani, Christopher Parrish, Nicolas Boisgerault, Tim Kottke, Jill Thompson, Esteban Celis and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

11 citing papers in PubMed, 12 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

16 authors at 5 institutions in 2 countries.

Shane ZaidiDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA; Targeted Therapy Team, Division of Cancer Biology, The Institute of Cancer Research, London, UK.
Miran BlanchardDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Kevin ShimDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Elizabeth IlettDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA; Targeted and Biological Therapies Group, Leeds Institute of Cancer and Pathology, St. James' University Hospital, Leeds, UK.
Karishma RajaniDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Christopher ParrishTargeted and Biological Therapies Group, Leeds Institute of Cancer and Pathology, St. James' University Hospital, Leeds, UK.
Nicolas BoisgeraultDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Tim KottkeDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Jill ThompsonDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Esteban CelisCancer Immunology, Inflammation and Tolerance Program, Georgia Regents University Cancer Center, Augusta, Georgia, USA.
Jose PulidoDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Peter SelbyTargeted and Biological Therapies Group, Leeds Institute of Cancer and Pathology, St. James' University Hospital, Leeds, UK.
Hardev PandhaLeggett Building, Faculty of Health and Medical Sciences, University of Surrey, Guildford, UK.
Alan MelcherTargeted and Biological Therapies Group, Leeds Institute of Cancer and Pathology, St. James' University Hospital, Leeds, UK.
Kevin HarringtonTargeted Therapy Team, Division of Cancer Biology, The Institute of Cancer Research, London, UK.
Richard VileDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA; Targeted and Biological Therapies Group, Leeds Institute of Cancer and Pathology, St. James' University Hospital, Leeds, UK; Department of Immunology, Mayo Clinic, Rochester, Minnesota, USA. Electronic address: vile.richard@mayo.edu.
Mayo Clinic · USSt James's University Hospital · GBInstitute of Cancer Research · GBGeorgia Regents Medical Center · USUniversity of Surrey · GB

Funding

T Cell Based Carriers for In Vivo Gene Therapy of CancerR01CA107082 · NCI · MAYO CLINIC ROCHESTER · PI VILE, RICHARD G. · 2005 to 2014
$2.5M
Autoimmunity and anti tumor immunity outside of the melanocyte/melanoma paradigmR01CA132734 · NCI · MAYO CLINIC ROCHESTER · PI VILE, RICHARD G. · 2008 to 2012
$1.5M
Enhancing Systemic Delivery of Oncolytic Viruses for Cancer TherapyR01CA130878 · NCI · MAYO CLINIC ROCHESTER · PI VILE, RICHARD G. · 2009 to 2013
$1.4M
Enhancing Therapy of Primary and Recurrent Tumors With Systemic Oncolytic VirusR01CA175386 · NCI · MAYO CLINIC ROCHESTER · PI VILE, RICHARD G. · 2014 to 2018
$1.3M
Department of Health RP-PG-0707-10101NCI NIH HHS R01 CA107082NCI NIH HHS R01CA107082NCI NIH HHS R01 CA130878NCI NIH HHS R01CA130878NCI NIH HHS R01 CA132734NCI NIH HHS R01CA132734NCI NIH HHS R01 CA175386NCI NIH HHS R01CA175386-01A1
6 · The paper itself

Abstract

We used a VSV-cDNA library to treat recurrent melanoma, identifying immunogenic antigens, allowing us to target recurrences with immunotherapy or chemotherapy. Primary B16 melanoma tumors were induced to regress by frontline therapy. Mice with recurrent tumors were treated with VSV-cDNA immunotherapy. A Th17 recall response was used to screen the VSV-cDNA library for individual viruses encoding rejection antigens, subsequently targeted using immunotherapy or chemotherapy. Recurrent tumors were effectively treated with a VSV-cDNA library using cDNA from recurrent B16 tumors. Recurrence-associated rejection antigens identified included Topoisomerase-IIα, YB-1, cdc7 kinase, and BRAF. Fourteen out of 16 recurrent tumors carried BRAF mutations (595-605 region) following frontline therapy, even though the parental B16 tumors were BRAF wild type. The emergence of mutated BRAF-containing recurrences served as an excellent target for BRAF-specific immune-(VSV-BRAF), or chemo-(PLX-4720) therapies. Successful PLX-4720 therapy of recurrent tumors was associated with the development of a broad spectrum of T-cell responses. VSV-cDNA technology can be used to identify recurrence specific antigens. Emergence of mutated BRAF may be a major effector of melanoma recurrence which could serve as a target for chemo or immune therapy. This study suggests a rationale for offering patients with initially wild-type BRAF melanomas an additional biopsy to screen for mutant BRAF upon recurrence.

Indexed as

MutationAmino Acid SequenceAmino Acid SubstitutionAnimalsAntigens, NeoplasmAntineoplastic AgentsBase SequenceCancer VaccinesCell Line, TumorDisease Models, AnimalDrug Resistance, NeoplasmGanciclovirGene ExpressionHumansImmunologic FactorsMaleAntigens, NeoplasmAntineoplastic AgentsCancer VaccinesGanciclovirImmunologic FactorsProto-Oncogene Proteins B-rafThymidine Kinase

Identifiers

PMID25544599
PMCPMC4427869
OpenAlexW2136320993

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.