Evidence map›Paper›PMID 40927720›Full record

ReviewFrontiers in immunology2025

Viral warfare: unleashing engineered oncolytic viruses to outsmart cancer's defenses.

Tolulope O Omolekan, Joy T Folahan, Mulu Z Tesfay, Harikrishnan Mohan, Ojasvi Dutta, Leila Rahimian, Khandoker Usran Ferdous, Reza Ghavimi, Aleksandra Cios, Timothy K Beng and 7 more

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2025. 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.

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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

17 authors.

Tolulope O OmolekanDepartment of Pathological Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA, United States.
Joy T FolahanDepartment of Pathological Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA, United States.
Mulu Z TesfayDepartment of Pathology, University of Arkansas for Medical Sciences (UAMS), Little Rock, AR, United States.
Harikrishnan MohanDepartment of Pathological Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA, United States.
Ojasvi DuttaDepartment of Pathological Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA, United States.
Leila RahimianDepartment of Pathological Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA, United States.
Khandoker Usran FerdousDepartment of Pathology, University of Arkansas for Medical Sciences (UAMS), Little Rock, AR, United States.
Reza GhavimiDepartment of Pathological Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA, United States.
Aleksandra CiosDepartment of Pharmacology and Physiology, University of Maryland School of Medicine, Baltimore, MD, United States.
Timothy K BengDepartment of Chemistry, Central Washington University, Ellensburg, WA, United States.
Joseph FrancisDepartment of Comparative Biological Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA, United States.
Oswald D'AuvergneDepartment of Biological Sciences and Chemistry, College of Sciences and Engineering, Southern University and A&M College, Baton Rouge, LA, United States.
Mitesh J BoradDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN, United States.
Konstantin G KousoulasDepartment of Pathological Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA, United States.
Stephen DiGiuseppeDivision of Biomedical Sciences, Edward Via College of Osteopathic Medicine, Monroe, LA, United States.
Bolni Marius NagaloDepartment of Pharmacology and Physiology, University of Maryland School of Medicine, Baltimore, MD, United States.
Jean Christopher ChamcheuDepartment of Pathological Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA, United States.

Funding

Harnessing the potential of pharmacological small molecules to amplify VSV-based oncolytic viral therapyR15CA290568 · NCI · SOUTHERN UNIV A&M COL BATON ROUGE · PI CHAMCHEU, JEAN CHRISTOPHER · 2024 to 2024
$409k
NCI NIH HHS R15 CA290568
6 · The paper itself

Abstract

Oncolytic virotherapy (OVT) has emerged as a promising and innovative cancer treatment strategy that harnesses engineered viruses to selectively infect, replicate within, and destroys malignant cells while sparing healthy tissues. Beyond direct oncolysis, oncolytic viruses (OVs) exploit tumor-specific metabolic, antiviral, and immunological vulnerabilities to reshape the tumor microenvironment (TME) and initiate systemic antitumor immunity. Despite promising results from preclinical and clinical studies, several barriers, including inefficient intratumoral virus delivery, immune clearance, and tumor heterogeneity, continue to limit the therapeutic advantages of OVT as a standalone modality and hindered its clinical success. Recent advances in OV engineering have enhanced viral tropism, immune evasion, and transgene delivery, enabling better tumor targeting and penetration and sustained immune activation in malignant tumors. Moreover, rational combination strategies with immune checkpoint inhibitors (ICIs), chemotherapeutics, and immunometabolic modulators are reshaping OVT into a versatile strategy for precision oncology. This review highlights the mechanistic innovations driving next-generation OV engineering, explores emerging combination regimens, and discusses future directions to overcome resistance and maximize clinical efficacy.

Indexed as

NeoplasmsOncolytic VirotherapyOncolytic VirusesAnimalsCombined Modality TherapyGenetic EngineeringHumansTumor Microenvironmentcancer immunotherapycancer therapycombination therapyengineered virusesimmune evasiononcolytic virusespharmacological treatmenttumor targeting

Identifiers

PMID40927720
PMCPMC12414947

What Socratic 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 Socratic graph.