Targeting adeno-associated virus and adenoviral gene therapy for hepatocellular carcinoma

被引:36
作者
Wang, Yi-Gang [1 ]
Huang, Pan-Pan [1 ]
Zhang, Rong [1 ]
Ma, Bu-Yun [1 ]
Zhou, Xiu-Mei [1 ]
Sun, Yan-Fang [1 ]
机构
[1] Zhejiang Sci Tech Univ, Sch Life Sci, Xinyuan Inst Med & Biotechnol, Hangzhou 310018, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Hepatocellular carcinoma; Adeno-associated virus; Adenovirus; Virus vectors; MANGANESE SUPEROXIDE-DISMUTASE; GOLGI PROTEIN 73; ONCOLYTIC ADENOVIRUS; ANTITUMOR-ACTIVITY; TELOMERASE ACTIVITY; LIVER-CANCER; IN-VITRO; TUMOR-GROWTH; REPLICATING ADENOVIRUS; MICRORNA DELIVERY;
D O I
10.3748/wjg.v22.i1.326
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Human hepatocellular carcinoma (HCC) heavily endangers human heath worldwide. HCC is one of most frequent cancers in China because patients with liver disease, such as chronic hepatitis, have the highest cancer susceptibility. Traditional therapeutic approaches have limited efficacy in advanced liver cancer, and novel strategies are urgently needed to improve the limited treatment options for HCC. This review summarizes the basic knowledge, current advances, and future challenges and prospects of adeno-associated virus (AAV) and adenoviruses as vectors for gene therapy of HCC. This paper also reviews the clinical trials of gene therapy using adenovirus vectors, immunotherapy, toxicity and immunological barriers for AAV and adenoviruses, and proposes several alternative strategies to overcome the therapeutic barriers to using AAV and adenoviruses as vectors.
引用
收藏
页码:326 / 337
页数:12
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