Inhibition of chemotherapy-related breast tumor EMT by application of redox-sensitive siRNA delivery system CSO-ss-SA/siRNA along with doxorubicin treatment.
- Author:
Xuan LIU
1
;
Xue-Qing ZHOU
1
;
Xu-Wei SHANG
1
;
Li WANG
1
;
Yi LI
1
;
Hong YUAN
1
;
Fu-Qiang HU
1
Author Information
- Publication Type:Journal Article
- Keywords: Doxorubicin; Tumor metastasis; Ras-related C3 botulinum toxin substrate 1 (RAC1); Epithelial-mesenchymal transition (EMT); Chitosan micelles; Small interfering RNA (siRNA)
- MeSH: Amines/chemistry*; Antineoplastic Agents/adverse effects*; Breast Neoplasms/pathology*; Chitosan/chemistry*; Doxorubicin/adverse effects*; Drug Delivery Systems; Epithelial-Mesenchymal Transition/drug effects*; Female; Humans; MCF-7 Cells; Neoplasm Metastasis/prevention & control*; Oxidation-Reduction; RNA, Small Interfering/administration & dosage*; Reactive Oxygen Species/metabolism*; rac1 GTP-Binding Protein/physiology*
- From: Journal of Zhejiang University. Science. B 2020;21(3):218-233
- CountryChina
- Language:English
- Abstract: Metastasis is one of the main reasons causing death in cancer patients. It was reported that chemotherapy might induce metastasis. In order to uncover the mechanism of chemotherapy-induced metastasis and find solutions to inhibit treatment-induced metastasis, the relationship between epithelial-mesenchymal transition (EMT) and doxorubicin (DOX) treatment was investigated and a redox-sensitive small interfering RNA (siRNA) delivery system was designed. DOX-related reactive oxygen species (ROS) were found to be responsible for the invasiveness of tumor cells in vitro, causing enhanced EMT and cytoskeleton reconstruction regulated by Ras-related C3 botulinum toxin substrate 1 (RAC1). In order to decrease RAC1, a redox-sensitive glycolipid drug delivery system (chitosan-ss-stearylamine conjugate (CSO-ss-SA)) was designed to carry siRNA, forming a gene delivery system (CSO-ss-SA/siRNA) downregulating RAC1. CSO-ss-SA/siRNA exhibited an enhanced redox sensitivity compared to nonresponsive complexes in 10 mmol/L glutathione (GSH) and showed a significant safety. CSO-ss-SA/siRNA could effectively transmit siRNA into tumor cells, reducing the expression of RAC1 protein by 38.2% and decreasing the number of tumor-induced invasion cells by 42.5%. When combined with DOX, CSO-ss-SA/siRNA remarkably inhibited the chemotherapy-induced EMT in vivo and enhanced therapeutic efficiency. The present study indicates that RAC1 protein is a key regulator of chemotherapy-induced EMT and CSO-ss-SA/siRNA silencing RAC1 could efficiently decrease the tumor metastasis risk after chemotherapy.
