1. Enhancing CRISPR/Cas gene editing through modulating cellular mechanical properties for cancer therapy
- Author
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Di Zhang, Guoxun Wang, Xueliang Yu, Tuo Wei, Lukas Farbiak, Lindsay T. Johnson, Alan Mark Taylor, Jiazhu Xu, Yi Hong, Hao Zhu, and Daniel J. Siegwart
- Subjects
Gene Editing ,Gene Transfer Techniques ,Biomedical Engineering ,Bioengineering ,Condensed Matter Physics ,B7-H1 Antigen ,Atomic and Molecular Physics, and Optics ,Mice ,Neoplasms ,Liposomes ,Animals ,Nanoparticles ,General Materials Science ,CRISPR-Cas Systems ,Electrical and Electronic Engineering - Abstract
Genome editing holds great potential for cancer treatment due to the ability to precisely inactivate or repair cancer-related genes. However, delivery of CRISPR/Cas to solid tumours for efficient cancer therapy remains challenging. Here we targeted tumour tissue mechanics via a multiplexed dendrimer lipid nanoparticle (LNP) approach involving co-delivery of focal adhesion kinase (FAK) siRNA, Cas9 mRNA and sgRNA (siFAK + CRISPR-LNPs) to enable tumour delivery and enhance gene-editing efficacy. We show that gene editing was enhanced10-fold in tumour spheroids due to increased cellular uptake and tumour penetration of nanoparticles mediated by FAK-knockdown. siFAK + CRISPR-PD-L1-LNPs reduced extracellular matrix stiffness and efficiently disrupted PD-L1 expression by CRISPR/Cas gene editing, which significantly inhibited tumour growth and metastasis in four mouse models of cancer. Overall, we provide evidence that modulating the stiffness of tumour tissue can enhance gene editing in tumours, which offers a new strategy for synergistic LNPs and other nanoparticle systems to treat cancer using gene editing.
- Published
- 2022