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Ultrasound-Sensitive Targeted Liposomes as a Gene Delivery System for the Synergistic Treatment of Hepatocellular Carcinoma.
Wang, Guannan; Lu, Hongtong; Pan, Yong; Qi, Yanxin; Huang, Yubin.
Afiliação
  • Wang G; Faculty of Chemistry, Northeast Normal University, Changchun, 130024, P. R. China.
  • Lu H; Faculty of Chemistry, Northeast Normal University, Changchun, 130024, P. R. China.
  • Pan Y; Faculty of Chemistry, Northeast Normal University, Changchun, 130024, P. R. China.
  • Qi Y; Faculty of Chemistry, Northeast Normal University, Changchun, 130024, P. R. China.
  • Huang Y; Faculty of Chemistry, Northeast Normal University, Changchun, 130024, P. R. China.
Small ; : e2406182, 2024 Aug 27.
Article em En | MEDLINE | ID: mdl-39189532
ABSTRACT
Gene therapy and sonodynamic therapy, as emerging treatment methods, have great potential in cancer treatment. However, there are significant challenges in the in vivo delivery of genes and sonosensitizers during the treatment process, which ultimately affects the therapeutic outcome. In this study, an ultrasound-sensitive targeted liposome nanoparticle system (MLipsiBcl-2) is developed to deliver the sonosensitizers and siRNA for the synergistic treatment of hepatocellular carcinoma. Generation of reactive oxygen species (ROS) by MLipsiBcl-2 can be initiated through ultrasound stimulation, leading to liposome rupture and release of the sonosensitizer and small interfering RNA (siRNA). Furthermore, ROS can disrupt lysosomal membranes, facilitating gene release for downregulating overexpressed antiapoptotic protein levels in cancer cells. Experimental results from in vitro and in vivo studies demonstrated the efficacy of synergistic treatment on hepatocellular carcinoma cells and the high biocompatibility of MLipsiBcl-2 under ultrasound stimulation. The advancement of this ultrasound-sensitive targeted gene delivery system shows potential as a versatile therapeutic platform that is easily operable, presenting a prospect for a synergistic treatment approach across various cancer types.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article