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Published on: October 11, 2013
Newcastle disease virus strain AF2240 as an oncolytic virus: A review
Jeevanathan Kalyanasundram1, Aini Hamid2, Khatijah Yusoff3
1Department of Microbiology, Faculty of Biotechnology and Biomolecular Sciences, Universiti Putra Malaysia, 43400, UPM Serdang, Selangor D.E., Malaysia; Malaysian Genome Institute, Jalan Bangi, 43000 Kajang, Selangor D.E., Malaysia.
Abstract:
The discovery of tumour selective virus-mediated apoptosis marked the birth of an alternative cancer treatment in the form of oncolytic viruses. Even though, its oncolytic efficiency was demonstrated more than 50 years ago, safety concerns which resulted from mild to lethal side effects hampered the progress of oncolytic virus research. Since the classical oncolytic virus studies rely heavily on its natural oncolytic ability, virus manipulation was limited, thereby, restricted efforts to improve its safety. In order to circumvent such restriction, experiments involving non-human viruses such as the avian Newcastle disease virus (NDV) was conducted using cultured cells, animal models and human subjects. The corresponding reports on its significant tumour cytotoxicity along with impressive safety profile initiated immense research interest in the field of oncolytic NDV. The varying degree of oncolytic efficiency and virulency among NDV strains encouraged researchers from all around the world to experiment with their respective local NDV isolates in order to develop an oncolytic virus with desirable characteristics. Such desirable features include high tumour-killing ability, selectivity and low systemic cytotoxicity. The Malaysian field outbreak isolate, NDV strain AF2240, also currently, receives significant research attention. Apart from its high cytotoxicity against tumour cells, this strain also provided fundamental insight into NDV-mediated apoptosis mechanism which involves Bax protein recruitment as well as death receptor engagement. Studies on its ability to selectively induce apoptosis in tumour cells also resulted in a proposed p38 MAPK/NF-κB/IκBα pathway. The immunogenicity of AF2240 was also investigated through PBMC stimulation and macrophage infection. In addition, the enhanced oncolytic ability of this strain under hypoxic condition signifies its dynamic tumour tropism. This review is aimed to introduce and discuss the aforementioned details of the oncolytic AF2240 strain along with its current challenges which outlines the future research direction of this virus.
Insights
Oncolytic Newcastle disease virus (NDV) offers a promising cancer therapy. The NDV strain AF2240 shows high tumor-killing ability and a good safety profile, advancing oncolytic virus research.
Area of Science:
- Oncology
- Virology
- Immunology
Background:
- Oncolytic viruses offer a novel cancer treatment, but safety concerns have limited progress.
- Newcastle disease virus (NDV) has emerged as a promising candidate due to its tumor selectivity and safety.
- Research focuses on optimizing NDV strains for enhanced efficacy and reduced toxicity.
Purpose of the Study:
- To review the potential of NDV strain AF2240 as an oncolytic virus.
- To discuss its tumor cytotoxicity, apoptosis mechanisms, and immunogenicity.
- To outline current challenges and future research directions for oncolytic NDV.
Main Methods:
- In vitro studies using cultured cells.
- In vivo studies using animal models.
- Analysis of apoptosis pathways and immunogenicity.
Main Results:
- NDV strain AF2240 demonstrates significant tumor cytotoxicity and selective apoptosis induction.
- The mechanism involves Bax recruitment, death receptor engagement, and the p38 MAPK/NF-κB/IκBα pathway.
- AF2240 exhibits enhanced oncolytic activity under hypoxia, indicating dynamic tumor tropism.
Conclusions:
- NDV strain AF2240 is a potent oncolytic virus with a favorable safety profile.
- Further research is needed to overcome challenges and optimize its therapeutic application.
- AF2240 holds significant promise for developing effective oncolytic virotherapy.
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