Efficient CRISPR/Cas9 gene-chemo synergistic cancer therapy via a stimuli-responsive chitosan-based nanocomplex elicits anti-tumorigenic pathway effect

• Published in: Chemical engineering journal (Lausanne, Switzerland : 1996) Vol. 393; p. 124688
• Main Authors: Zhang, Bing-Chen, Wu, Peng-Yu, Zou, Jun-Jie, Jiang, Jia-Li, Zhao, Rui-Rui, Luo, Bang-Yue, Liao, Yu-Qin, Shao, Jing-Wei
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 01.08.2020
• Subjects: Co-delivery nanosystem; CRISPR/Cas9 system; Gene-chemo synergistic therapy; HCC treatment; Paclitaxel; Co-delivery nanosystem; HCC treatment; CRISPR/Cas9 system; Gene-chemo synergistic therapy; Paclitaxel
• DOI: 10.1016/j.cej.2020.124688
• ISSN: 1385-8947

[Display omitted] •Nanocomplex for co-delivery of CRISPR/Cas9 and paclitaxel was constructed.•The nanosystem triggered efficient gene-editing with good safety.•The gene therapy of VEGFR2 sensitized the treatment effect of paclitaxel.•The nanosystem exhibited the synergistic modulation for IL-6-IL-8/NF-κB pathway.•The nanosystem achieved significant synergistic gene-chemo HCC treatment. Clustered regularly interspaced short palindromic repeat (CRISPR)-associated Cas9 nuclease system (CRISPR/Cas9) has become a powerful toolbox as a gene fixed-point knock-out method and hold the promising prospect for cancer therapy. However, the biological safety of the viral vectors and the instability of exogenous plasmid in blood circulation limits its application. Herein, we reported a lactobionic acid functionalized and stimuli-responsive chitosan based nanocomplex to co-deliver sgVEGFR2/Cas9 plasmid and paclitaxel for hepatoma carcinoma therapy. The genome editing efficiency of sgVEGFR2/Cas9 in the nanosystem achieved up to 38.6% of HepG2 cells in vitro and 33.4% of tumor tissues in vivo. The nanocomplex suppressed >60% VEGFR2 protein expression of HepG2 cells and inhibited hepatoma carcinoma (HCC) tumor progress by 70% on mice. In vivo study indicated the obvious tumor accumulation and the good biosafety of the nanosystem. Moreover, the gene-drug co-loaded nanoparticles stimulate anti-tumorigenic pathway of HCC by suppressing pro-inflammatory cytokines (IL-6/IL-8) and tumor angiogenesis-related protein (NF-κB p65) expression, which revealed the potential pathway inhibition of PTX when combined with the gene therapy for overexpression VEGFR2 on HCC cells. Overall, this strategy provided a versatile method for high efficiency CRISPR/Cas9 system delivery and showed tremendous application prospect for gene-chemo synergistic therapy.