Evidence map›Paper›PMID 36569326›Full record

ReviewFrontiers in pharmacology2022

Comprehensive assessment on the applications of oncolytic viruses for cancer immunotherapy.

Richard Kolade Omole, Oluwaseyi Oluwatola, Millicent Tambari Akere, Joseph Eniafe, Elizabeth Oladoyin Agboluaje, Oluwafemi Bamidele Daramola, Yemisi Juliet Ayantunji, Temiloluwa Ifeoluwa Omotade, Nkem Torimiro, Modupe Stella Ayilara and 2 more

Abstract readReview
In one paragraph

Review in Frontiers in pharmacology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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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

12 authors.

Richard Kolade OmoleDepartment of Microbiology, Obafemi Awolowo University, Ile-Ife, Nigeria.
Oluwaseyi OluwatolaDepartment of Molecular Medicine, Morsani College of Medicine, University of South Florida, Tampa, FL, United States.
Millicent Tambari AkereDepartment of Medicinal and Biological Chemistry, University of Toledo, Toledo, OH, United States.
Joseph EniafeDepartment of Microbiology and Immunology, Louisiana State University Health Sciences Center, Shreveport, LA, United States.
Elizabeth Oladoyin AgboluajeDepartment of Pharmaceutical and Biomedical Sciences, University of Georgia, Athens, GA, United States.
Oluwafemi Bamidele DaramolaDepartment of Microbiology, Obafemi Awolowo University, Ile-Ife, Nigeria.
Yemisi Juliet AyantunjiDepartment of Microbiology, Obafemi Awolowo University, Ile-Ife, Nigeria.
Temiloluwa Ifeoluwa OmotadeDepartment of Microbiology, Obafemi Awolowo University, Ile-Ife, Nigeria.
Nkem TorimiroDepartment of Microbiology, Obafemi Awolowo University, Ile-Ife, Nigeria.
Modupe Stella AyilaraFood Security and Safety Focus Area, Faculty of Natural and Agricultural Sciences, North-West University, Mmabatho, South Africa.
Oluwole Isaac AdeyemiDepartment of Pharmacology, Faculty of Pharmacy, Obafemi Awolowo University, Ile-Ife, Nigeria.
Olubusola Sajanat SalinsileMicrobiology Unit, Department of Applied Sciences, Osun State College of Technology, Esa-Oke, Nigeria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The worldwide burden of cancers is increasing at a very high rate, including the aggressive and resistant forms of cancers. Certain levels of breakthrough have been achieved with the conventional treatment methods being used to treat different forms of cancers, but with some limitations. These limitations include hazardous side effects, destruction of non-tumor healthy cells that are rapidly dividing and developing, tumor resistance to anti-cancer drugs, damage to tissues and organs, and so on. However, oncolytic viruses have emerged as a worthwhile immunotherapeutic option for the treatment of different types of cancers. In this treatment approach, oncolytic viruses are being modeled to target cancer cells with optimum cytotoxicity and spare normal cells with optimal safety, without the oncolytic viruses themselves being killed by the host immune defense system. Oncolytic viral infection of the cancer cells are also being genetically manipulated (either by removal or addition of certain genes into the oncolytic virus genome) to make the tumor more visible and available for attack by the host immune cells. Hence, different variants of these viruses are being developed to optimize their antitumor effects. In this review, we examined how grave the burden of cancer is on a global level, particularly in sub-Saharan Africa, major conventional therapeutic approaches to the treatment of cancer and their individual drawbacks. We discussed the mechanisms of action employed by these oncolytic viruses and different viruses that have found their relevance in the fight against various forms of cancers. Some pre-clinical and clinical trials that involve oncolytic viruses in cancer management were reported. This review also examined the toxicity and safety concerns surrounding the adoption of oncolytic viro-immunotherapy for the treatment of cancers and the likely future directions for researchers and general audience who wants updated information.

Indexed as

anti-cancercancerimmunologyoncolytic virustargeted killingtreatmenttumor microenvironmentviro-immunotherapy

Identifiers

PMID36569326
PMCPMC9772532

What OpenQuestion holds

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Registered trials

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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.