广州医药 ›› 2023, Vol. 54 ›› Issue (3): 8-13.DOI: 10.3969/j.issn.1000-8535.2023.03.002

• 专家综述 • 上一篇    下一篇

基因编辑在非酒精性脂肪性肝病动物模型构建中的应用及研究进展

李兴会1,2, 郭晨1,2, 陈汉清1,2   

  1. 1 广州市第一人民医院医学研究与创新转化中心(广州 510180)
    2 华南理工大学附属第二医院消化内科(广州 510180)
  • 收稿日期:2022-12-10 出版日期:2023-03-20 发布日期:2023-04-14
  • 通讯作者: 陈汉清,E-mail: chenhq921@163.com
  • 作者简介:陈汉清,博士,华南理工大学附属第二医院(广州市第一人民医院),研究员,博士生导师。美国波士顿大学医学院和得州大学圣安东尼奥健康科学中心博士后,北京市海外引进高层次人才(青年项目),广州市青年后备人才,广州市医学骨干人才,国家自然科学基金评审专家。主要从事消化系统疾病发病机制及精准治疗研究。近5年共主持包括2项国自然等7项科研项目。共发表SCI 论文 40 余篇,其中,以第一作者/通讯作者在HepatologyNano TodaySmallCancer Science等发表SCI论文21篇,其中IF>10有7篇。担任 Frontiers in PharmacologyFrontiers in EndocrinologyFrontiers in Chemistry客座主编,Journal of Clinical and Translational Hepatology和《广州医药》编委,iMetaHepatobiliary & Pancreatic Diseases International青年编委。
  • 基金资助:
    国家自然科学基金青年科学项目(82000250);国家自然科学基金面上项目(32171370);广东省自然科学基金面上项目(2021A1515011005,2022A1515010415)

Research progress of genome editing for constructing the animal models of nonalcoholic fatty liver disease

LI Xinghui1,2, GUO Chen1,2, CHEN Hanqing1,2   

  1. 1 Center for Medical Research on Innovation and Translation, Guangzhou First People's Hospital, Guangzhou 510180, China
    2 Department of Gastroenterology and Hepatology, the Second Affiliated Hospital, School of Medicine, South China University of Technology, Guangzhou 510180, China
  • Received:2022-12-10 Online:2023-03-20 Published:2023-04-14

摘要: 非酒精性脂肪性肝病(NAFLD)是世界范围内慢性肝病的一个主要原因,约15%的NAFLD患者会发展为非酒精性脂肪性肝炎、肝纤维化、肝硬化甚至肝癌。目前其发病及进展机制尚未明确,也无有效治疗手段。因此,构建临床前NAFLD动物模型至关重要,有助于为NAFLD提供临床治疗的新方案。本文将系统分析目前已构建的NAFLD动物模型在临床前研究中的局限性,并重点总结和综述基于基因编辑在NAFLD动物模型构建中的应用及研究进展,这对于探讨NAFLD发病机制及新药研发具有重要的临床意义。

关键词: 非酒精性脂肪性肝病, 动物模型, 基因编辑

Abstract: Nonalcoholic fatty liver disease (NAFLD) is a leading cause of chronic liver disease worldwide, and about 15% of NAFLD patients will develop into nonalcoholic steatohepatitis, hepatic fibrosis, cirrhosis, and ultimately hepatocellular carcinoma. However, the biological mechanism of the pathogenesis and progression of NAFLD is not fully understood, and there are still no effective or targeted therapies for NAFLD. Therefore, it is an urgent need to construct pre-clinical animal models of NAFLD, which will help to better understand and explore the potential therapeutic strategy in the treatment of NAFLD. Here, we summarize the recent advances and limitations of the established animal models of NAFLD and focus on the potential application and research progress of genome editing for constructing the animal models of NAFLD. There animal models will be very useful to reveal the pathologic mechanism of human NAFLD, and to screen new therapeutic drugs.

Key words: nonalcoholic fatty liver disease, animal model, genome editing