Cell Membrane-Camouflaged Chitosan-Polypyrrole Nanogels Co-Deliver Drug and Gene for Targeted Chemotherapy and Bone Metastasis Inhibition of Prostate Cancer.
Qiuyu YuYue GaoWaicong DaiDanni LiLu ZhangMeera Moydeen Abdul HameedRui GuoMin LiuXiangyang ShiXueyan CaoPublished in: Advanced healthcare materials (2024)
The development of functional nanoplatforms to improve the chemotherapy outcome and inhibit distal cancer cell metastasis remains an extreme challenge in cancer management. In this work, a human-derived PC-3 cancer cell membrane-camouflaged chitosan-polypyrrole nanogel (CH-PPy NG) platform, which can be loaded with chemotherapeutic drug docetaxel (DTX) and RANK siRNA for targeted chemotherapy and gene silencing-mediated metastasis inhibition of late-stage prostate cancer in a mouse model, is reported. The prepared NGs with a size of 155.8 nm show good biocompatibility, pH-responsive drug release profile, and homologous targeting specificity to cancer cells, allowing for efficient and precise drug/gene co-delivery. Through in-vivo antitumor treatment in a xenografted PC-3 mouse tumor model, it is shown that such a CH-PPy NG-facilitated co-delivery system allows for effective chemotherapy to slow down the tumor growth rate, and effectively inhibits the metastasis of prostate cancer to the bone via downregulation of the RANK/RANKL signaling pathway. The created CH-Ppy NGs may be utilized as a promising platform for enhanced chemotherapy and anti-metastasis treatment of prostate cancer.
Keyphrases
- prostate cancer
- locally advanced
- drug delivery
- radical prostatectomy
- cancer therapy
- drug release
- signaling pathway
- mouse model
- papillary thyroid
- rectal cancer
- high throughput
- squamous cell carcinoma
- copy number
- cell proliferation
- chemotherapy induced
- endothelial cells
- drug induced
- epithelial mesenchymal transition
- climate change
- body composition
- gene expression
- dna damage
- squamous cell
- emergency department
- pi k akt
- immune response
- dna repair
- wound healing
- transcription factor
- oxidative stress
- combination therapy
- childhood cancer
- postmenopausal women
- gold nanoparticles
- inflammatory response
- induced apoptosis
- tandem mass spectrometry
- induced pluripotent stem cells
- electronic health record