Evidence map›Paper›PMID 33614913›Full record

ArticleMolecular therapy oncolytics2021

Combining vanadyl sulfate with Newcastle disease virus potentiates rapid innate immune-mediated regression with curative potential in murine cancer models.

Thomas M McAusland, Jacob P van Vloten, Lisa A Santry, Matthew M Guilleman, Amira D Rghei, Edgar M Ferreira, Joelle C Ingrao, Rozanne Arulanandam, Pierre P Major, Leonardo Susta and 4 more

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy oncolytics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
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  5. Review
  6. Molecular Circuits of Immune Sensing and Response to Oncolytic Virotherapy.International journal of molecular sciences · 2024
    Review
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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

14 authors at 3 institutions in 1 country.

Thomas M McAuslandDepartment of Pathobiology, University of Guelph, Guelph, ON N1G 2WI, Canada.
Jacob P van VlotenDepartment of Pathobiology, University of Guelph, Guelph, ON N1G 2WI, Canada.
Lisa A SantryDepartment of Pathobiology, University of Guelph, Guelph, ON N1G 2WI, Canada.
Matthew M GuillemanDepartment of Pathobiology, University of Guelph, Guelph, ON N1G 2WI, Canada.
Amira D RgheiDepartment of Pathobiology, University of Guelph, Guelph, ON N1G 2WI, Canada.
Edgar M FerreiraDepartment of Pathobiology, University of Guelph, Guelph, ON N1G 2WI, Canada.
Joelle C IngraoDepartment of Pathobiology, University of Guelph, Guelph, ON N1G 2WI, Canada.
Rozanne ArulanandamCenter for Innovative Cancer Research, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
Pierre P MajorJuravinski Cancer Centre, 699 Concession Street, Hamilton, ON L8V 5C2, Canada.
Leonardo SustaDepartment of Pathobiology, University of Guelph, Guelph, ON N1G 2WI, Canada.
Khalil KarimiDepartment of Pathobiology, University of Guelph, Guelph, ON N1G 2WI, Canada.
Jean-Simon DialloCenter for Innovative Cancer Research, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
Byram W BridleDepartment of Pathobiology, University of Guelph, Guelph, ON N1G 2WI, Canada.
Sarah K WoottonDepartment of Pathobiology, University of Guelph, Guelph, ON N1G 2WI, Canada.
University of Guelph · CAUniversity of Ottawa · CAJuravinski Cancer Centre · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The avian paramyxovirus, Newcastle disease virus (NDV), is a promising oncolytic agent that has been shown to be safe and effective in a variety of pre-clinical cancer models and human clinical trials. NDV preferentially replicates in tumor cells due to signaling defects in apoptotic and antiviral pathways acquired during the transformation process and is a potent immunostimulatory agent. However, when used as a monotherapy NDV lacks the ability to consistently generate durable remissions. Here we investigate the use of viral sensitizer-mediated combination therapy to enhance the anti-neoplastic efficacy of NDV. Intratumoral injection of vanadyl sulfate, a pan-inhibitor of protein tyrosine phosphatases, in combination with NDV significantly increased the number and activation status of natural killer (NK) cells in the tumor microenvironment, concomitant with increased expression of interferon-β, granulocyte-macrophage colony-stimulating factor, and monocyte chemoattractant protein-1, leading to rapid tumor regression and long-term cures in mice bearing syngeneic B16-F10 melanomas. The anti-tumor efficacy of this combination therapy was abrogated when NK cells were depleted and when interferon-β expression was transiently suppressed. Tumor-specific CD8

Indexed as

B16-F10combination therapyNewcastle disease virus (NDV)vanadyl sulfate

Identifiers

PMID33614913
PMCPMC7868934
OpenAlexW3125433041

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.