Evidence map›Paper›PMID 37313455›Full record

ArticleMolecular therapy oncolytics2023

Trap and ambush therapy using sequential primary and tumor escape-selective oncolytic viruses.

Mason J Webb, Timothy Kottke, Benjamin L Kendall, Jack Swanson, Chisom Uzendu, Jason Tonne, Jill Thompson, Muriel Metko, Madelyn Moore, Mitesh Borad and 5 more

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy oncolytics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

7 citing papers in PubMed, 6 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

15 authors at 3 institutions in 1 country.

Mason J WebbDivision of Hematology/Medical Oncology, Mayo Clinic, Rochester, MN 55905, USA.
Timothy KottkeDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Benjamin L KendallDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Jack SwansonDepartment of Immunology, Mayo Clinic, Rochester, MN 55905, USA.
Chisom UzenduDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Jason TonneDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Jill ThompsonDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Muriel MetkoDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Madelyn MooreDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Mitesh BoradDivision of Hematology/Oncology, Mayo Clinic, Scottsdale, AZ 85259, USA.
Lewis RobertsDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN 55905, USA.
Rosa M DiazDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Michael OlinDivision of Pediatric Hematology and Oncology, University of Minnesota, Minneapolis, MN 55455, USA.
Antonella BorgattiDepartment of Veterinary Clinical Sciences, University of Minnesota, St. Paul, MN 55108, USA.
Richard VileDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Mayo Clinic in Arizona · USMayo Clinic · USUniversity of Minnesota · US

Funding

Project 4: ImmunovirotherapyP50CA210964 · NCI · MAYO CLINIC ROCHESTER · PI MARK A. MC NIVEN · 2018 to 2026
$20.5M
Characterizing the role of CSDE1 as a critical co-factor for VSV replication.R01AI170535 · NIAID · MAYO CLINIC ROCHESTER · PI Richard G. Vile · 2023 to 2026
$1.6M
Re-purposing Oncolytic Virotherapy to Re-invigorate CAR T Cell Therapy for Solid Tumors.R01CA269384 · NCI · MAYO CLINIC ROCHESTER · PI Richard G. Vile · 2023 to 2026
$1.4M
Research Training Program in Neuro-OncologyT32CA217836 · NCI · MAYO CLINIC ROCHESTER · PI O'NEILL, BRIAN PATRICK, VILE, RICHARD G. · 2018 to 2022
$1.4M
PhD Training Program in Virology and Gene TherapyT32AI132165 · NIAID · MAYO CLINIC ROCHESTER · PI ROBERTO B. CATTANEO · 2018 to 2026
$1.3M
Novel Strategies to Treat Diffuse Midline Glioma with CAR T Cell TherapyR21CA262994 · NCI · MAYO CLINIC ROCHESTER · PI VILE, RICHARD G. · 2021 to 2022
$405k
Defining Antigen-Dependent and Antigen-Independent Mechanisms for EGFRviii-Expressing Tumor Escape From TherapyF31CA271560 · NCI · MAYO CLINIC ROCHESTER · PI SWANSON, JACK H · 2022 to 2024
$126k
NCI NIH HHS F31 CA271560NCI NIH HHS P50 CA210964NCI NIH HHS R01 CA269384NCI NIH HHS R21 CA262994NCI NIH HHS T32 CA217836NIAID NIH HHS R01 AI170535NIAID NIH HHS T32 AI132165
6 · The paper itself

Abstract

In multiple models of oncolytic virotherapy, it is common to see an early anti-tumor response followed by recurrence. We have previously shown that frontline treatment with oncolytic VSV-IFN-β induces APOBEC proteins, promoting the selection of specific mutations that allow tumor escape. Of these mutations in B16 melanoma escape (ESC) cells, a C-T point mutation in the cold shock domain-containing E1 (

Indexed as

CD200AR-LCSDE1immunotherapymelanomaoncolytic virotherapytumor escapevesicular stomatitis virusVSV

Identifiers

PMID37313455
PMCPMC10258242
OpenAlexW4377293387

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.