Cell membrane based biomimetic nanocomposites for targeted therapy of drug resistant EGFR-mutated lung cancer.
Pengying WuDongtao YinJiaming LiuHuige ZhouMengyu GuoJing LiuYang LiuXiaobing WangYing LiuChunying ChenPublished in: Nanoscale (2019)
The therapeutic efficacy of anti-cancer nanomedicines is generally constrained due to limited accumulation in the solid tumors. In this study, we developed a biomimetic nano-carrier to enhance the chemo-therapeutic efficacy of doxorubicin and icotinib in a chemo-resistant non-small cell lung cancer (NSCLC) cell line harboring a mutation in the epidermal growth factor receptor (EGFR). The unique nanomedicine was prepared by coating with targeting cancer cell membrane proteins as highly specific ligands. The resulting biomimetic nanoparticles were highly stable and exhibited superior homologous targeting ability in vitro compared with control groups. In a mouse EGFR-mutated NSCLC xenograft model, intravenous injection of the biomimetic nanomedicine led to a high tumour inhibition rate (87.56%). Histopathological analysis demonstrated that the biomimetic nanomedicine had minimal side effects. Taken together, a cancer cell membrane-based biomimetic drug carrier can significantly enhance drug accumulation and improve therapeutic efficacy in cancers.
Keyphrases
- epidermal growth factor receptor
- cancer therapy
- small cell lung cancer
- advanced non small cell lung cancer
- drug resistant
- tyrosine kinase
- drug delivery
- tissue engineering
- papillary thyroid
- multidrug resistant
- photodynamic therapy
- squamous cell
- acinetobacter baumannii
- high dose
- dna damage
- emergency department
- lymph node metastasis
- dna repair
- drug induced
- cystic fibrosis
- gold nanoparticles
- ultrasound guided