Syncytia Formation in Oncolytic Virotherapy

被引:22
|
作者
Burton, Chase [1 ]
Bartee, Eric [1 ]
机构
[1] Med Univ South Carolina, Dept Microbiol & Immunol, Room 208C,Basic Sci Bldg, Charleston, SC 29425 USA
来源
关键词
NEWCASTLE-DISEASE VIRUS; VESICULAR STOMATITIS-VIRUS; HERPES-SIMPLEX-VIRUS; FUSOGENIC MEMBRANE GLYCOPROTEIN; ASCITES TUMOR-CELLS; CANCER STEM-CELLS; FUSION PROTEIN; ANTITUMOR-ACTIVITY; INTRATUMORAL EXPRESSION; PRODRUG ACTIVATION;
D O I
10.1016/j.omto.2019.09.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:131 / 139
页数:9
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