Evidence map›Paper›PMID 30209859›Full record

ReviewReviews in medical virology2018

Defects in interferon pathways as potential biomarkers of sensitivity to oncolytic viruses.

Olga V Matveeva, Peter M Chumakov

Erratum issuedOpen access · bronzeAbstract readReview
In one paragraph

Review in Reviews in medical virology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 69 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed, 1 pooled it
5.2field-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

69 citing papers in PubMed, 1 synthesis or guideline pooled it, 98 citations in OpenAlex.

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9 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 2 countries.

Olga V MatveevaBiopolymer Design LLC, Acton, MA, USA.ORCID 0000-0001-8555-9847
Peter M ChumakovEngelhardt Institute of Molecular Biology, Moscow, Russia.ORCID 0000-0002-8078-2908
Acton Institute · USEngelhardt Institute of Molecular Biology · RU

Funding

The Ministry of Healthcare of the Russian Federation 1.1096
6 · The paper itself

Abstract

Increased sensitivity of cancer cells to viruses is a prerequisite for the success of oncolytic virotherapy. One of the major causes of such a phenotype is the disruption of innate antiviral defenses associated with dysfunction of type 1 interferons (IFNs) that permits unlimited replication of viruses in cancer cells. Defects in IFN pathways help cancer progression by providing additional advantages to tumor cells. However, while these defects promote the survival and accelerated proliferation of malignant cells, they facilitate viral replication and thus enhance the efficiency of viral oncolysis. This review describes a broad spectrum of defects in genes that participate in IFN induction and IFN response pathways. Expression levels and/or functional activities of these genes are frequently low or absent in cancer cells, making them sensitive to virus infection. Therefore, certain specific defects in IFN signaling cascades might serve as potential biomarkers to help in identifying individual cancer patients who are likely to benefit from oncolytic virotherapy.

Indexed as

Antineoplastic AgentsBiomarkersHumansInterferonsNeoplasmsOncolytic VirotherapyOncolytic VirusesAntineoplastic AgentsBiomarkersInterferonsbiomarkersdefects in IFN inductiondefects in IFN pathwaysdefects in IFN responseIFN defects in cancer cellmalfunction of IFN signaling cascadeoncolytic virotherapyoncolytic virusesviral oncolysis

Identifiers

PMID30209859
PMCPMC6906582
OpenAlexW2890022744

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.