Evidence map›Paper›PMID 28203321›Full record

ArticleAmerican journal of virology2016

The Practical Consideration of Poliovirus as an Oncolytic Virotherapy.

Elizabeth Denniston, Hannah Crewdson, Nicole Rucinsky, Andrew Stegman, Diana Remenar, Katherine Moio, Brianne Clark, Alexandra Higginbotham, Ross Keffer, Sarah Brammer and 1 more

Abstract read
In one paragraph

Article in American journal of virology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
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

11 authors.

Elizabeth DennistonDepartment of Graduate Health Sciences, West Liberty University, West Liberty, WV, USA.
Hannah CrewdsonDepartment of Graduate Health Sciences, West Liberty University, West Liberty, WV, USA.
Nicole RucinskyDepartment of Graduate Health Sciences, West Liberty University, West Liberty, WV, USA.
Andrew StegmanDepartment of Graduate Health Sciences, West Liberty University, West Liberty, WV, USA.
Diana RemenarDepartment of Graduate Health Sciences, West Liberty University, West Liberty, WV, USA.
Katherine MoioDepartment of Graduate Health Sciences, West Liberty University, West Liberty, WV, USA.
Brianne ClarkDepartment of Graduate Health Sciences, West Liberty University, West Liberty, WV, USA.
Alexandra HigginbothamDepartment of Graduate Health Sciences, West Liberty University, West Liberty, WV, USA.
Ross KefferDepartment of Graduate Health Sciences, West Liberty University, West Liberty, WV, USA.
Sarah BrammerDepartment of Graduate Health Sciences, West Liberty University, West Liberty, WV, USA.
Joseph HorzempaDepartment of Graduate Health Sciences, West Liberty University, West Liberty, WV, USA; Department of Natural Sciences and Mathematics, West Liberty University, West Liberty, WV, USA.

Funding

WV INBRE: The Inhibitor of Growth Family Member 4 (ING4) inhibits L-Type Amino Acid Transporter 1 (LAT1) expression to suppress Breast CancerP20GM103434 · NIGMS · MARSHALL UNIVERSITY · PI GARY O RANKIN · 2012 to 2026
$61.1M
NIGMS NIH HHS P20 GM103434
6 · The paper itself

Abstract

The inauguration of novel treatment strategies into the clinical setting faces a number of hurdles. In addition to treatment efficacy and safety, acceptance by doctors and patients is paramount to the success of novel therapies. Although viruses are the cause of numerous infectious diseases, these acellular entities have been harnessed over the years to benefit mankind. Recently, a recombinant Poliovirus-Rhinovirus Chimera (PVSRIPO) has shown promise for the treatment of glioblastoma in clinical trials as well as other cancer types in animal models. In this literature review, we discuss the use of PVSRIPO as an oncolytic virotherapy. In addition to being a potential treatment for glioblastoma, this recombinant virus could possibly be used against other cancers because many tumor cells express the PVSRIPO receptor antigens (CD155) and have a limited ability to control viral replication. Moreover, virus-induced immune responses contribute to the efficacy of PVSRIPO. Given the current trajectory of this experimental therapy, the possibility exists that PVSRIPO will soon be a viable treatment option for various cancer types. While many healthcare providers and cancer patients likely welcome this new viral based treatment, history has taught us that some may be skeptical and avoid its use because of the viral composition of this therapy.

Indexed as

GlioblastomaOncolytic VirologyPoliovirusPVSRIPO

Identifiers

PMID28203321
PMCPMC5304422

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.