Bioorthogonal CRISPR/Cas9-Drug Conjugate: A Combinatorial Nanomedicine Platform.
Marcel Janis BehaJoo-Chan KimSan Hae ImYunsu KimSeungju YangJuhee LeeYu Ri NamHaeshin LeeHee-Sung ParkHyun Jung ChungPublished in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2023)
Bioconjugation of proteins can substantially expand the opportunities in biopharmaceutical development, however, applications are limited for the gene editing machinery despite its tremendous therapeutic potential. Here, a self-delivered nanomedicine platform based on bioorthogonal CRISPR/Cas9 conjugates, which can be armed with a chemotherapeutic drug for combinatorial therapy is introduced. It is demonstrated that multi-functionalized Cas9 with a drug and polymer can form self-condensed nanocomplexes, and induce significant gene editing upon delivery while avoiding the use of a conventional carrier formulation. It is shown that the nanomedicine platform can be applied for combinatorial therapy by incorporating the anti-cancer drug olaparib and targeting the RAD52 gene, leading to significant anti-tumor effects in BRCA-mutant cancer. The current development provides a versatile nanomedicine platform for combination treatment of human diseases such as cancer.
Keyphrases
- crispr cas
- cancer therapy
- genome editing
- high throughput
- papillary thyroid
- drug delivery
- endothelial cells
- adverse drug
- stem cells
- dna damage
- drug induced
- emergency department
- squamous cell carcinoma
- genome wide
- single cell
- high resolution
- dna methylation
- dna repair
- lymph node metastasis
- young adults
- childhood cancer
- copy number
- wild type
- replacement therapy