Tumor cell-targeted delivery of CRISPR/Cas9 by aptamer-functionalized lipopolymer for therapeutic genome editing of VEGFA in osteosarcoma

C Liang, F Li, L Wang, ZK Zhang, C Wang, B He, J Li… - Biomaterials, 2017 - Elsevier
Osteosarcoma (OS) is a highly aggressive pediatric cancer, characterized by frequent lung
metastasis and pathologic bone destruction. Vascular endothelial growth factor A (VEGFA) …

Lipid nanoparticle-mediated efficient delivery of CRISPR/Cas9 for tumor therapy

L Zhang, P Wang, Q Feng, N Wang, Z Chen… - NPG Asia …, 2017 - nature.com
The emerging CRISPR/Cas9 system represents a promising platform for genome editing.
However, its low transfection efficiency is a major problem hampering the application of the …

Engineered nanomaterials to potentiate CRISPR/Cas9 gene editing for cancer therapy

K Yi, H Kong, YH Lao, D Li, RL Mintz, T Fang… - Advanced …, 2024 - Wiley Online Library
Clustered regularly interspaced short palindromic repeats/associated protein 9
(CRISPR/Cas9) gene‐editing technology shows promise for manipulating single or multiple …

Non-viral delivery systems for CRISPR/Cas9-based genome editing: Challenges and opportunities

L Li, S Hu, X Chen - Biomaterials, 2018 - Elsevier
In recent years, CRISPR (clustered regularly interspaced short palindromic repeat)/Cas
(CRISPR-associated) genome editing systems have become one of the most robust …

Engineered extracellular vesicle-delivered CRISPR/Cas9 for radiotherapy sensitization of glioblastoma

X Liu, Z Cao, W Wang, C Zou, Y Wang, L Pan, B Jia… - ACS …, 2023 - ACS Publications
Radiotherapy is a mainstay of glioblastoma (GBM) treatment; however, the development of
therapeutic resistance has hampered the efficacy of radiotherapy, suggesting that additional …

Biomaterial-assisted targeted and controlled delivery of CRISPR/Cas9 for precise gene editing

Z Iqbal, K Rehman, J Xia, M Shabbir, M Zaman… - Biomaterials …, 2023 - pubs.rsc.org
RISPR-Cas9 has exhibited enormous potential in gene therapy. It can perform genome
editing with single-nucleotide precision in various types of cell and tissue, providing a …

CRISPR-Cas9 genome editing using targeted lipid nanoparticles for cancer therapy

D Rosenblum, A Gutkin, R Kedmi, S Ramishetti… - Science …, 2020 - science.org
Harnessing CRISPR-Cas9 technology for cancer therapeutics has been hampered by low
editing efficiency in tumors and potential toxicity of existing delivery systems. Here, we …

Effective PEI-mediated delivery of CRISPR-Cas9 complex for targeted gene therapy

N Ryu, MA Kim, D Park, B Lee, YR Kim, KH Kim… - … , Biology and Medicine, 2018 - Elsevier
The-state-of-art CRISPR/Cas9 is one of the most powerful among the approaches being
developed to rescue fundamental causes of gene-based inheritable diseases. Several …

Brain-targeted CRISPR/Cas9 nanomedicine for effective glioblastoma therapy

W Ruan, M Jiao, S Xu, M Ismail, X Xie, Y An… - Journal of Controlled …, 2022 - Elsevier
CRISPR/Cas9 gene-editing technology shows great potential for treating a variety of
diseases, such as glioblastoma multiforme (GBM). However, CRISPR components suffer …

Tropism-facilitated delivery of CRISPR/Cas9 system with chimeric antigen receptor-extracellular vesicles against B-cell malignancies

Q Xu, Z Zhang, L Zhao, Y Qin, H Cai, Z Geng… - Journal of Controlled …, 2020 - Elsevier
The CRISPR/Cas9 system is an efficient genome-editing system that has been successfully
applied in the field of gene therapy. However, clinical applications of the CRISPR/Cas9 …