» Articles » PMID: 31890866

Syncytia Formation in Oncolytic Virotherapy

Overview
Publisher Cell Press
Date 2020 Jan 1
PMID 31890866
Citations 21
Authors
Affiliations
Soon will be listed here.
Abstract

Oncolytic virotherapy uses replication-competent virus as a means of treating cancer. Whereas this field has shown great promise as a viable treatment method, the limited spread of these viruses throughout the tumor microenvironment remains a major challenge. To overcome this issue, researchers have begun looking at syncytia formation as a novel method of increasing viral spread. Several naturally occurring fusogenic viruses have been shown to possess strong oncolytic potential and have since been studied to gain insight into how this process benefits oncolytic virotherapy. Whereas these naturally fusogenic viruses have been beneficial, there are still challenges associated with their regular use. Because of this, engineered/recombinant fusogenic viruses have also been created that enhance nonfusogenic oncolytic viruses with the beneficial property of syncytia formation. The purpose of this review is to examine the existing body of literature on syncytia formation in oncolytics and offer direction for potential future studies.

Citing Articles

Fusogenic vesicular stomatitis virus combined with natural killer T cell immunotherapy controls metastatic breast cancer.

Nelson A, McMullen N, Gebremeskel S, De Antueno R, MacKenzie D, Duncan R Breast Cancer Res. 2024; 26(1):78.

PMID: 38750591 PMC: 11094881. DOI: 10.1186/s13058-024-01818-5.


Histone deacetylase inhibitor boosts anticancer potential of fusogenic oncolytic vaccinia virus by enhancing cell-cell fusion.

Nakatake M, Kurosaki H, Nakamura T Cancer Sci. 2023; 115(2):600-610.

PMID: 38037288 PMC: 10859623. DOI: 10.1111/cas.16032.


Cell Fusion and Syncytia Formation in Cancer.

Sieler M, Dittmar T Results Probl Cell Differ. 2023; 71:433-465.

PMID: 37996689 DOI: 10.1007/978-3-031-37936-9_20.


Mechanisms of Cell Fusion in Cancer.

Noubissi F, Odubanjo O, Ogle B, Tchounwou P Results Probl Cell Differ. 2023; 71:407-432.

PMID: 37996688 PMC: 10893907. DOI: 10.1007/978-3-031-37936-9_19.


Clinical Advances and Future Directions of Oncolytic Virotherapy for Head and Neck Cancer.

Wang Z, Sun P, Li Z, Xiao S Cancers (Basel). 2023; 15(21).

PMID: 37958464 PMC: 10650136. DOI: 10.3390/cancers15215291.


References
1.
Tong Y, Qian W . Targeting cancer stem cells with oncolytic virus. Stem Cell Investig. 2016; 1:20. PMC: 4923666. DOI: 10.3978/j.issn.2306-9759.2014.11.01. View

2.
Zhu B, Yang J, Fu X, Jiang Y . Anti-tumor effects of gene therapy with GALV membrane fusion glycoprotein in lung adenocarcinoma. Cell Biochem Biophys. 2014; 69(3):577-82. DOI: 10.1007/s12013-014-9835-5. View

3.
Altomonte J, Marozin S, Schmid R, Ebert O . Engineered newcastle disease virus as an improved oncolytic agent against hepatocellular carcinoma. Mol Ther. 2009; 18(2):275-84. PMC: 2839313. DOI: 10.1038/mt.2009.231. View

4.
Cram L, Forslund J, Jett J . Quantification of cell fusion by twenty-one strains of Newcastle disease virus using flow microfluorometry. J Gen Virol. 1978; 41(1):27-36. DOI: 10.1099/0022-1317-41-1-27. View

5.
Nakamori M, Fu X, Meng F, Jin A, Tao L, Bast Jr R . Effective therapy of metastatic ovarian cancer with an oncolytic herpes simplex virus incorporating two membrane fusion mechanisms. Clin Cancer Res. 2003; 9(7):2727-33. View