Literature DB >> 22348553

Advances in liver-directed gene therapy for hepatocellular carcinoma by non-viral delivery systems.

Buyun Ding1, Tao Li, Jian Zhang, Lixia Zhao, Guangxi Zhai.   

Abstract

Hepatocellular carcinoma (HCC) is a malignancy with a high mortality. Gene therapy provides a promising way for the treatment of HCC. Efficient gene delivery system, suitable gene target and appropriate way of administration together determine the effect of gene therapy for HCC. In recent years, employing non-viral gene delivery systems in gene therapy for HCC has attracted a lot of attention. Compared with viral vectors, non-viral gene delivery systems are nearly non-immunogenic, relatively safer, less expensive to produce and can carry a good many of genetic materials. But the transfection efficiency of these vectors still needs to be improved. And the liver targeting is another problem that needs to be solved. Attaching ligands to the non-viral vectors to enhance the targeting ability to the specific receptor and targeting to molecular targets of HCC are the effective strategies. Adopting suitable ways of administration is also a factor that plays an important role to achieve liver targeting. This review introduced the advances in liver-targeted gene therapy by non-viral vectors including the efforts to overcome the low transfection efficiency and enhance the liver targeting effect.

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Year:  2012        PMID: 22348553     DOI: 10.2174/156652312800099625

Source DB:  PubMed          Journal:  Curr Gene Ther        ISSN: 1566-5232            Impact factor:   4.391


  6 in total

1.  ApoE-modified liposomes mediate the antitumour effect of survivin promoter-driven HSVtk in hepatocellular carcinoma.

Authors:  Xiuli Mu; Xi Wang; Yan Wei; Chaochao Wen; Qi Zhang; Chunyang Xu; Chang Liu; Chan Zhang; Fanxiu Meng; Na Zhao; Tao Gong; Rui Guo; Gongqin Sun; Gaopeng Li; Hongwei Zhang; Qin Qin; Jun Xu; Xiushan Dong; Lumei Wang; Baofeng Yu
Journal:  Cancer Gene Ther       Date:  2019-10-23       Impact factor: 5.987

Review 2.  Liver-targeted gene therapy: Approaches and challenges.

Authors:  Rajagopal N Aravalli; John D Belcher; Clifford J Steer
Journal:  Liver Transpl       Date:  2015-06       Impact factor: 6.112

3.  Asialoglycoprotein receptor-magnetic dual targeting nanoparticles for delivery of RASSF1A to hepatocellular carcinoma.

Authors:  Wan-Jiang Xue; Ying Feng; Fei Wang; Yi-Bing Guo; Peng Li; Lei Wang; Yi-Fei Liu; Zhi-Wei Wang; Yu-Min Yang; Qin-Sheng Mao
Journal:  Sci Rep       Date:  2016-02-26       Impact factor: 4.379

4.  Exosome-mediated delivery of Cas9 ribonucleoprotein complexes for tissue-specific gene therapy of liver diseases.

Authors:  Tao Wan; Jiafeng Zhong; Qi Pan; Tianhua Zhou; Yuan Ping; Xiangrui Liu
Journal:  Sci Adv       Date:  2022-09-14       Impact factor: 14.957

5.  MicroRNA-regulated non-viral vectors with improved tumor specificity in an orthotopic rat model of hepatocellular carcinoma.

Authors:  J A Ronald; R Katzenberg; C H Nielsen; H J Jae; L V Hofmann; S S Gambhir
Journal:  Gene Ther       Date:  2013-05-30       Impact factor: 5.250

6.  miR‑378 in combination with ultrasonic irradiation and SonoVue microbubbles transfection inhibits hepatoma cell growth.

Authors:  Jianjun Wang; Yunchun Li; Qianfeng Ma; Jiaxin Huang
Journal:  Mol Med Rep       Date:  2020-03-30       Impact factor: 2.952

  6 in total

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