Evidence map›Paper›PMID 29473868›Full record

ReviewViruses2018

Oncotargeting by Vesicular Stomatitis Virus (VSV): Advances in Cancer Therapy.

Suman Bishnoi, Ritudhwaj Tiwari, Sharad Gupta, Siddappa N Byrareddy, Debasis Nayak

Open access · goldAbstract readReview
In one paragraph

Review in Viruses, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 1 pooled it
8.9field-weighted citation impact, top 2% 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

64 citing papers in PubMed, 1 synthesis or guideline pooled it, 112 citations in OpenAlex.

  1. Pooled it
  2. Review
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  6. Article
  7. Review
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  12. Article
  13. Article
  14. Activation and Evasion of the FEAR Pathway by RNA Viruses.bioRxiv : the preprint server for biology · 2025
    Article
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  19. Article
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4 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 2 countries.

Suman BishnoiDiscipline of Bioscience and Biomedical Engineering, Indian Institute of Technology Indore, Indore, MP 453 552, India. phd1501171015@iiti.ac.in.
Ritudhwaj TiwariDiscipline of Bioscience and Biomedical Engineering, Indian Institute of Technology Indore, Indore, MP 453 552, India. phd1501171001@iiti.ac.in.
Sharad GuptaDiscipline of Bioscience and Biomedical Engineering, Indian Institute of Technology Indore, Indore, MP 453 552, India. shgupta@iiti.ac.in.
Siddappa N ByrareddyDepartment of Pharmacology and Experimental Neurosciences, University of Nebraska Medical Center, Omaha, NE 68130, USA. sid.byrareddy@unmc.edu.
Debasis NayakDiscipline of Bioscience and Biomedical Engineering, Indian Institute of Technology Indore, Indore, MP 453 552, India. nayakdn@iiti.ac.in.
Indian Institute of Technology Indore · INUniversity of Nebraska Medical Center · US

Funding

Role of HIV Env glycosylation in mucosal transmissionR01AI113883 · NIAID · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BYRAREDDY, SIDDAPPA N · 2014 to 2018
$3.9M
NIAID NIH HHS R01 AI113883
6 · The paper itself

Abstract

Modern oncotherapy approaches are based on inducing controlled apoptosis in tumor cells. Although a number of apoptosis-induction approaches are available, site-specific delivery of therapeutic agents still remain the biggest hurdle in achieving the desired cancer treatment benefit. Additionally, systemic treatment-induced toxicity remains a major limiting factor in chemotherapy. To specifically address drug-accessibility and chemotherapy side effects, oncolytic virotherapy (OV) has emerged as a novel cancer treatment alternative. In OV, recombinant viruses with higher replication capacity and stronger lytic properties are being considered for tumor cell-targeting and subsequent cell lysing. Successful application of OVs lies in achieving strict tumor-specific tropism called oncotropism, which is contingent upon the biophysical interactions of tumor cell surface receptors with viral receptors and subsequent replication of oncolytic viruses in cancer cells. In this direction, few viral vector platforms have been developed and some of these have entered pre-clinical/clinical trials. Among these, the Vesicular stomatitis virus (VSV)-based platform shows high promise, as it is not pathogenic to humans. Further, modern molecular biology techniques such as reverse genetics tools have favorably advanced this field by creating efficient recombinant VSVs for OV; some have entered into clinical trials. In this review, we discuss the current status of VSV based oncotherapy, challenges, and future perspectives regarding its therapeutic applications in the cancer treatment.

Indexed as

Oncolytic VirotherapyAnimalsApoptosisBiomarkers, TumorGenetic VectorsHumansImmune SystemImmunomodulationInterferon Type IMiceMolecular Targeted TherapyNeoplasmsOncolytic VirusesSignal TransductionVesicular stomatitis Indiana virusBiomarkers, TumorInterferon Type Iapoptosisoncolytic virusoncotherapytumor lysisvesicular stomatitis virus (VSV)

Identifiers

PMID29473868
PMCPMC5850397
OpenAlexW2793321136

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.