Novel Lipid Nanocomplex Co-Carrying Bcl2 siRNA and Quantum Dots for EGF Receptor-Targeted Anti-Cancer Theranosis.
Moon Jung ChoiSeong Jae KangYeon Kyung LeeKang Chan ChoiDo Hyun LeeHwa Yeon JeongMin Woo KimKeun Sik KimYong Serk ParkPublished in: International journal of molecular sciences (2024)
Many different types of nanoparticles have been suggested for tumor-targeted theranosis. However, most systems were prepared through a series of complicated processes and could not even overcome the blood-immune barriers. For the accurate diagnosis and effective treatment of cancers, herein we suggested the lipid micellar structure capturing quantum dot (QD) for cancer theranosis. The QD/lipid micelles (QDMs) were prepared using a simple self-assembly procedure and then conjugated with anti-epidermal growth factor receptor (EGFR) antibodies for tumor targeting. As a therapeutic agent, Bcl2 siRNA-cholesterol conjugates were loaded on the surface of QDMs. The EGFR-directed QDMs containing Bcl2 siRNA, so-called immuno-QDM/siBcl2 (iQDM/siBcl2), exhibited the more effective delivery of QDs and siBcl2 to target human colorectal cancer cells in cultures as well as in mouse xenografts. The effective in vivo targeting of iQDM/siBcl2 resulted in a more enhanced therapeutic efficacy of siBcl2 to the target cancer in mice. Based on the results, anti-EGFR QDM capturing therapeutic siRNA could be suggested as an alternative modality for tumor-targeted theranosis.
Keyphrases
- cancer therapy
- epidermal growth factor receptor
- drug delivery
- tyrosine kinase
- advanced non small cell lung cancer
- small cell lung cancer
- papillary thyroid
- quantum dots
- fatty acid
- endothelial cells
- squamous cell carcinoma
- childhood cancer
- lymph node metastasis
- photodynamic therapy
- high resolution
- minimally invasive
- drug release
- metabolic syndrome
- growth factor
- sensitive detection
- skeletal muscle
- induced pluripotent stem cells
- wound healing
- insulin resistance