Evidence map›Paper›PMID 30835721›Full record

ArticlePLoS computational biology2019

In vitro and in silico multidimensional modeling of oncolytic tumor virotherapy dynamics.

David R Berg, Chetan P Offord, Iris Kemler, Matthew K Ennis, Lawrence Chang, George Paulik, Zeljko Bajzer, Claudia Neuhauser, David Dingli

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

16 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Oncolytic viruses: advanced strategies in cancer therapy.Signal transduction and targeted therapy · 2026
    Review
  4. Spatially structured models of viral dynamics: a scoping review.Microbiology and molecular biology reviews : MMBR · 2025
    Article
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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

9 authors at 4 institutions in 1 country.

David R BergDepartment of Information Technology, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0002-5959-0864
Chetan P OffordMolecular Medicine, Mayo Clinic, Rochester, Minnesota.
Iris KemlerMolecular Medicine, Mayo Clinic, Rochester, Minnesota.
Matthew K EnnisMolecular Medicine, Mayo Clinic, Rochester, Minnesota.
Lawrence ChangMolecular Medicine, Mayo Clinic, Rochester, Minnesota.
George PaulikInternational Business Machines, Rochester, Minnesota.ORCID 0000-0002-4300-7929
Zeljko BajzerDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota.
Claudia NeuhauserDepartment of Mathematics, University of Houston, Houston, Texas.
David DingliMolecular Medicine, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0001-7477-3004
Mayo Clinic · USBoston Medical Center · USIBM (United States) · USUniversity of Houston · US

Funding

Molecular imaging and system dynamics of tumor virotherapyR01CA164241 · NCI · MAYO CLINIC ROCHESTER · PI DINGLI, DAVID J · 2011 to 2015
$2.5M
NCI NIH HHS R01 CA164241
6 · The paper itself

Abstract

Tumor therapy with replication competent viruses is an exciting approach to cancer eradication where viruses are engineered to specifically infect, replicate, spread and kill tumor cells. The outcome of tumor virotherapy is complex due to the variable interactions between the cancer cell and virus populations as well as the immune response. Oncolytic viruses are highly efficient in killing tumor cells in vitro, especially in a 2D monolayer of tumor cells, their efficiency is significantly lower in a 3D environment, both in vitro and in vivo. This indicates that the spatial dimension may have a major influence on the dynamics of virus spread. We study the dynamic behavior of a spatially explicit computational model of tumor and virus interactions using a combination of in vitro 2D and 3D experimental studies to inform the models. We determine the number of nearest neighbor tumor cells in 2D (median = 6) and 3D tumor spheroids (median = 16) and how this influences virus spread and the outcome of therapy. The parameter range leading to tumor eradication is small and even harder to achieve in 3D. The lower efficiency in 3D exists despite the presence of many more adjacent cells in the 3D environment that results in a shorter time to reach equilibrium. The mean field mathematical models generally used to describe tumor virotherapy appear to provide an overoptimistic view of the outcomes of therapy. Three dimensional space provides a significant barrier to efficient and complete virus spread within tumors and needs to be explicitly taken into account for virus optimization to achieve the desired outcome of therapy.

Indexed as

Computer SimulationModels, BiologicalOncolytic VirotherapyCell Line, TumorHumansIn Vitro TechniquesLentivirusMeasles virusNeoplasmsSpheroids, CellularTumor MicroenvironmentVirus Replication

Identifiers

PMID30835721
PMCPMC6400333
OpenAlexW2918848243

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.