Abstract
Here, we investigated the effects of dual delivery of IGF-1R siRNA and doxorubicin by chitosan nanoparticles on viability of A549 lung cancer cells line by utilization of MTT and qRT-PCR. Furthermore apoptosis and migration of treated cells were assessed by Annexin-PI and wound healing assays, respectively. The chitosan nanoparticles had about 176 nm size with zeta potential and polydispersive index about 11 mV and 0.3, respectively. The IGF-1R siRNA had synergistic effect on DOX-induced cytotoxicity and apoptosis in tumour cells. In addition, siRNA/DOX-loaded chitosan nanoparticles could significantly decrease migration and expressions of mmp9, VEGF and STAT3 in A549 cells.
Author supplied keywords
Cite
CITATION STYLE
Shali, H., Shabani, M., Pourgholi, F., Hajivalili, M., Aghebati-Maleki, L., Jadidi-Niaragh, F., … Yousefi, M. (2018). Co-delivery of insulin-like growth factor 1 receptor specific siRNA and doxorubicin using chitosan-based nanoparticles enhanced anticancer efficacy in A549 lung cancer cell line. Artificial Cells, Nanomedicine and Biotechnology, 46(2), 293–302. https://doi.org/10.1080/21691401.2017.1307212
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.