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Updated: Apr 19, 2026

Lentiviral Vector-mediated Gene Therapy of Hepatocytes Ex Vivo for Autologous Transplantation in Swine
Published on: November 4, 2018
Current status of gene therapy for hepatocellular carcinoma, with a focus on gene delivery approaches
Xiaoyu Wang, Zongguang Tai, Wei Zhang
1Department of Pharmaceutics, Changhai Hospital, 168# Changhai Road, Shanghai 200433, China. liullk@126.com.
Abstract:
Hepatocellular carcinoma (HCC) is a malignancy with high morbidity and mortality rates, especially in East Asia. Gene therapy is a potential approach for treating HCC. An efficient and safe gene delivery method is a crucial factor for HCC gene therapy. In recent years, gene delivery systems, including viral and non-viral gene vectors, bacteria, and physical methods, have undergone substantial development. Among them, various non-viral vectors have been studied widely and in detail because they are relatively safe and have a high capacity. In this review, we focus on current and emerging HCC delivery techniques and address the challenges involved in the use and improvement of non-viral vectors.
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