Author:
Chu Zhili,Yang Sihui,Li Qianru,Shang Jianing,Ren Zilong,Ren Feng
Abstract
Abstract
Background
Newcastle disease virus (NDV) is an oncolytic virus that can inhibit cancer cell proliferation and kill cancer cells. The NDV nonstructural V protein can regulate viral replication; however, whether the V protein contributes to NDV oncolysis is unclear.
Results
This study revealed that NDV inhibited tumor cell proliferation and that V protein expression promoted the proliferation of HepG2 cells, as determined at the single-cell level. In addition, to identify the regulatory mechanism of the V protein in HepG2 cells, transcriptome sequencing was performed and indicated that the expression/activation of multiple cell proliferation-related genes/signaling pathways were changed in cells overexpressing the V protein. Hence, the MAPK and WNT signaling pathways were selected for verification, and after blocking these two signaling pathways with inhibitors, the V protein promotion of cell proliferation was found to be attenuated.
Conclusions
The results showed that the V protein regulated the proliferation of cancer cells through multiple signaling pathways, providing valuable references for future studies on the mechanism by which the V protein regulates cancer cell proliferation.
Funder
Study on the mechanism of oncolytic Newcastle disease virus selective cell infection
The mechanism of oncolytic Newcastle disease virus V protein targeting MAPK-ERK1/2 signaling pathway to regulate the proliferation of hepatocellular carcinoma cells
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Genetics,Oncology
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