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Translational Medicine / 转化医学Adenoviral p53 Gene Therapy, Gendicine

Zhaohui Peng

PhD

🏢Shenzhen SiBiono GeneTech🌐China

Chief Scientist

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Key Papers
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Key Contributions

👥Biography 个人简介

Zhaohui Peng led the development of Gendicine (recombinant human p53 adenovirus), the world's first commercially approved gene therapy product, receiving Chinese SFDA approval in 2003 for treatment of head and neck squamous cell carcinoma. Gendicine delivers wild-type p53 tumor suppressor gene via replication-defective adenoviral vector to restore p53-dependent apoptosis in p53-mutant tumors. Clinical data from thousands of treated patients have demonstrated that Gendicine combined with radiation or chemotherapy improves response rates in head and neck, liver, and lung cancers. His work pioneered the regulatory pathway for gene therapy approval and demonstrated the clinical feasibility of tumor suppressor gene replacement therapy.

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🧪Research Fields 研究领域

Gendicine adenoviral p53 gene therapy
tumor suppressor gene replacement
p53 gene therapy head neck cancer
recombinant adenovirus Ad-p53
gene therapy regulatory approval China

🎓Key Contributions 主要贡献

Representative Works 代表性著作

📄Data Sources 数据来源

Last updated: 2026-04-01 | All information from publicly available academic sources

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