Evidence map›Paper›PMID 33566625›Full record

ArticleMolecular pharmaceutics2021

Bluetongue Virus Particles as Nanoreactors for Enzyme Delivery and Cancer Therapy.

Eva C Thuenemann, Duc H T Le, George P Lomonossoff, Nicole F Steinmetz

Open access · greenAbstract read
In one paragraph

Article in Molecular pharmaceutics, 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
6.9field-weighted citation impact, top 4% 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, 25 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

4 authors at 3 institutions in 3 countries.

Eva C ThuenemannDepartment of Biological Chemistry, John Innes Centre, Norwich Research Park, NR4 7UH Colney, United Kingdom.
Duc H T LeDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, Ohio 44106, United States.ORCID 0000-0002-3539-0462
George P LomonossoffDepartment of Biological Chemistry, John Innes Centre, Norwich Research Park, NR4 7UH Colney, United Kingdom.
Nicole F SteinmetzDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, Ohio 44106, United States.ORCID 0000-0002-0130-0481
John Innes Centre · GBCase Western Reserve University · USRadboud University Nijmegen · NL

Funding

Dual-pronged nano-drug delivery using plant virus-like particles.R01CA224605 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Nicole Franziska Steinmetz · 2017 to 2026
$4.0M
Biotechnology and Biological Sciences Research Council BB/L014130/1Biotechnology and Biological Sciences Research Council BBS/E/J/000PR9794NCI NIH HHS R01 CA224605
6 · The paper itself

Abstract

The side effects of chemotherapy can be reduced by targeting tumor cells with an enzyme (or the corresponding gene) that converts a nontoxic prodrug into a toxic drug inside the tumor cells, also killing the surrounding tumor cells via the bystander effect. Viruses are the most efficient gene delivery vehicles because they have evolved to transfer their own nucleic acids into cells, but their efficiency must be balanced against the risks of infection, the immunogenicity of nucleic acids, and the potential for genomic integration. We therefore tested the effectiveness of genome-free virus-like particles (VLPs) for the delivery of Herpes simplex virus 1 thymidine kinase (HSV1-TK), the most common enzyme used in prodrug conversion therapy. HSV1-TK is typically delivered as a gene, but in the context of VLPs, it must be delivered as a protein. We constructed VLPs and smaller core-like particles (CLPs) based on Bluetongue virus, with HSV1-TK fused to the inner capsid protein VP3. TK-CLPs and TK-VLPs could be produced in large quantities in plants. The TK-VLPs killed human glioblastoma cells efficiently in the presence of ganciclovir, with an IC

Indexed as

Adenosine TriphosphatasesAntiviral AgentsBluetongue virusCapsid ProteinsCell Line, TumorGanciclovirGenetic TherapyGene Transfer TechniquesGlioblastomaHerpesvirus 1, HumanHumansNanotechnologyPhosphorylationProdrugsThymidine KinaseTransfectionAdenosine TriphosphatasesAntiviral AgentsCapsid ProteinsGanciclovirProdrugsThymidine Kinasecore-like particle (CLP)ganciclovirthymidine kinase (TK)virus-directed enzyme prodrug therapy (VDEPT)virus-like particle (VLP)

Identifiers

PMID33566625
PMCPMC8086382
OpenAlexW3128688627

What OpenQuestion holds

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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.