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Updated: Jul 2, 2026

Genome-wide RNAi Screening to Identify Host Factors That Modulate Oncolytic Virus Therapy
Published on: April 3, 2018
Organoid-based platforms for oncolytic virus discovery and optimization: Bridging in vitro innovation and clinical
Fan Yang1, Hui Wang2, Yigang Wang1
1Gene Therapy Center, College of Life Science and Medicine, Zhejiang Sci-Tech University, Hangzhou 310018, Zhejiang, PR China.
Abstract:
Although oncolytic virus therapy has shown promising efficacy in preclinical studies, its clinical translation remains limited because conventional experimental models fail to replicate the human tumor microenvironment accurately. As an advanced three-dimensional culture system, organoid technology provides a powerful platform to address this challenge, as it retains the heterogeneity and microenvironmental features of primary tumors. This review systematically summarizes organoid modeling technology and highlights its critical role in the research and development of oncolytic viruses. The development of organoid biobanks, together with their integration into high-throughput screening systems, has facilitated rational viral engineering and targeted optimization through large-scale data analysis. In clinical applications, patient-derived organoids have enabled personalized prediction of therapeutic responses by serving as functional models for drug testing. Despite ongoing challenges in protocol standardization and in accurately simulating the immune microenvironment, organoid technology is rapidly becoming a key bridge between basic research and clinical translation in oncolytic virotherapy, accelerating the development of next-generation oncolytic virus therapies.
Insights
Organoid technology accurately models human tumors, overcoming limitations in oncolytic virus therapy research. This approach accelerates the development of personalized oncolytic virus treatments by enabling better drug testing and prediction of therapeutic responses.
Area of Science:
- Oncology
- Virology
- Biotechnology
Background:
- Oncolytic virus therapy shows promise but faces clinical translation challenges due to inadequate preclinical models.
- Current models fail to replicate the complex human tumor microenvironment, limiting therapeutic development.
Purpose of the Study:
- To review organoid modeling technology for oncolytic virus research and development.
- To highlight the role of organoids in overcoming limitations of conventional experimental models.
Main Methods:
- Systematic review of organoid modeling techniques.
- Integration of organoid biobanks with high-throughput screening systems.
- Application of patient-derived organoids for drug testing and response prediction.
Main Results:
- Organoids retain tumor heterogeneity and microenvironmental features, offering a superior model.
- Organoid biobanks and screening systems facilitate viral engineering and optimization.
- Patient-derived organoids enable personalized prediction of therapeutic responses.
Conclusions:
- Organoid technology is crucial for advancing oncolytic virus therapy research and clinical translation.
- Despite challenges in standardization and immune simulation, organoids accelerate the development of next-generation therapies.
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