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Updated: May 29, 2026

Production of High-Titer Recombinant Newcastle Disease Virus from Allantoic Fluid
Published on: May 25, 2022
Apoptin enhances the oncolytic properties of Newcastle disease virus
Yantao Wu1, Xiaorong Zhang, Xiaobo Wang
1Ministry of Education Key Lab for Avian Preventive Medicine, College of Veterinary Medicine, Yangzhou University, Yangzhou, China.
Objective:
Naturally occurring strains of Newcastle disease virus (NDV) have demonstrated the potential to kill cancer cells in both preclinical and clinical studies. Previous studies showed that apoptin, the VP3 protein of chicken infectious anemia virus, is a p53-independent, Bcl-2-insensitive apoptotic protein with the ability to specifically induce apoptosis in transformed cells. In this study, we tested the hypothesis that apoptin enhances NDV-mediated tumor cell death.
Methods:
Reverse genetics was used to engineer an oncolytic NDV strain, FMW, to express apoptin. The antitumor effects of the recombinant virus (rFMW/AP) were also evaluated in the tumor cell lines and tumor-bearing mice.
Results:
Compared to the parental strain FMW, rFMW/AP was more potent in killing A459 and SMMC7721 tumor cells. Recombinant NDV also exhibited higher efficacy in suppressing tumor growth in mice bearing A549-induced tumors. Furthermore, rFMW/AP did not display apparent toxic effects in either normal cells or control mice.
Conclusion:
Our results suggest that the recombinant NDV expressing apoptin is a promising novel antitumor agent.
Insights
Engineered Newcastle disease virus (NDV) expressing apoptin shows enhanced tumor cell killing. This novel oncolytic virus effectively suppressed tumor growth in mice without apparent toxicity, indicating its potential as an antitumor agent.
Area of Science:
- Oncolytic virology
- Molecular oncology
- Viral gene therapy
Background:
- Naturally occurring Newcastle disease virus (NDV) strains exhibit oncolytic properties.
- Apoptin, a protein from chicken infectious anemia virus, induces apoptosis independently of p53 and Bcl-2 in cancer cells.
- Combining NDV with apoptin may enhance cancer cell death.
Purpose of the Study:
- To engineer an oncolytic NDV strain expressing apoptin.
- To evaluate the antitumor efficacy of the recombinant virus (rFMW/AP) in vitro and in vivo.
- To assess the safety profile of rFMW/AP.
Main Methods:
- Reverse genetics was employed to construct the recombinant NDV (rFMW/AP) expressing apoptin.
- In vitro studies utilized tumor cell lines (A459, SMMC7721) to assess cytotoxicity.
- In vivo studies involved tumor-bearing mice (A549-induced tumors) to evaluate tumor growth suppression.
Main Results:
- The recombinant rFMW/AP demonstrated increased potency in killing A459 and SMMC7721 tumor cells compared to the parental FMW strain.
- rFMW/AP significantly suppressed tumor growth in mice with A549-induced tumors.
- No apparent toxic effects were observed in normal cells or control mice treated with rFMW/AP.
Conclusions:
- The engineered NDV expressing apoptin (rFMW/AP) is a potent oncolytic virus.
- rFMW/AP shows enhanced antitumor efficacy and a favorable safety profile.
- This recombinant NDV represents a promising novel therapeutic agent for cancer treatment.
Related Concept Videos
The Extrinsic Apoptotic Pathway
Tumor Immunotherapy
Apoptosis
The Intrinsic Apoptotic Pathway

