Enhanced and Prolonged Antitumor Effect of Salinomycin-Loaded Gelatinase-Responsive Nanoparticles via Targeted Drug Delivery and Inhibition of Cervical Cancer Stem Cells
Qin Wang,1,* Fangcen Liu,2,* Lifeng Wang,1 Chen Xie,3 Puyuan Wu,1 Shiyao Du,1 Shujuan Zhou,1 Zhichen Sun,1 Qin Liu,1 Lixia Yu,1 Baorui Liu,1 Rutian Li1 1The Comprehensive Cancer Centre of Drum Tower Hospital, Medical School of Nanjing University, Clinical Cancer Institute of Nanjing University, Nanj...
| Main Authors: | , , , , , , , , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Dove Medical Press
2020-02-01
|
| Series: | International Journal of Nanomedicine |
| Subjects: | |
| Online Access: | https://www.dovepress.com/enhanced-and-prolonged-antitumor-effect-of-salinomycin-loaded-gelatina-peer-reviewed-article-IJN |
| _version_ | 1818424509419487232 |
|---|---|
| author | Wang Q Liu F Wang L Xie C Wu P Du S Zhou S Sun Z Liu Q Yu L Liu B Li R |
| author_facet | Wang Q Liu F Wang L Xie C Wu P Du S Zhou S Sun Z Liu Q Yu L Liu B Li R |
| author_sort | Wang Q |
| collection | DOAJ |
| description | Qin Wang,1,* Fangcen Liu,2,* Lifeng Wang,1 Chen Xie,3 Puyuan Wu,1 Shiyao Du,1 Shujuan Zhou,1 Zhichen Sun,1 Qin Liu,1 Lixia Yu,1 Baorui Liu,1 Rutian Li1 1The Comprehensive Cancer Centre of Drum Tower Hospital, Medical School of Nanjing University, Clinical Cancer Institute of Nanjing University, Nanjing 210008, People’s Republic of China; 2The Comprehensive Cancer Centre, Nanjing Drum Tower Hospital, Clinical College of Nanjing Medical University, Nanjing, People’s Republic of China; 3Key Laboratory for Organic Electronics and Information Displays, Institute of Advanced Materials (IAM), Jiangsu National Synergetic Innovation Center for Advanced Materials (SICAM), Nanjing University of Posts & Telecommunications, Nanjing 210023, People’s Republic of China*These authors contributed equally to this workCorrespondence: Rutian Li; Baorui LiuThe Comprehensive Cancer Centre of Drum Tower Hospital, Medical School of Nanjing University, Clinical Cancer Institute of Nanjing University, 321 Zhongshan Road, Nanjing 210008, People’s Republic of ChinaTel +86-25-83107081Fax +86-25-83317016Email rutianli@nju.edu.cn; baoruiliu@nju.edu.cnBackground: Cervical cancer stem cells (CCSCs) represent a subpopulation of tumor cells that possess self-renewal capacity and numerous intrinsic mechanisms of resistance to conventional chemotherapy and radiotherapy. These cells play a crucial role in relapse and metastasis of cervical cancer. Therefore, eradication of CCSCs is the primary objective in cervical cancer therapy. Salinomycin (Sal) is an agent used for the elimination of cancer stem cells (CSCs); however, the occurrence of several side effects hinders its application. Nanoscale drug-delivery systems offer great promise for the diagnosis and treatment of tumors. These systems can be used to reduce the side effects of Sal and improve clinical benefit.Methods: Sal-loaded polyethylene glycol-peptide-polycaprolactone nanoparticles (Sal NPs) were fabricated under mild and non-toxic conditions. The real-time biodistribution of Sal NPs was investigated through non-invasive near-infrared fluorescent imaging. The efficacy of tumor growth inhibition by Sal NPs was evaluated using tumor xenografts in nude mice. Flow cytometry, immunohistochemistry, and Western blotting were used to detect the apoptosis of CSCs after treatment with Sal NPs. Immunohistochemistry and Western blotting were used to examine epithelial–mesenchymal transition (epithelial interstitial transformation) signal-related molecules.Results: Sal NPs exhibited antitumor efficacy against cervical cancers by inducing apoptosis of CCSCs and inhibiting the epithelial–mesenchymal transition pathway. Besides, tumor pieces resected from Sal NP-treated mice showed decreased reseeding ability and growth speed, further demonstrating the significant inhibitory ability of Sal NPs against CSCs. Moreover, owing to targeted delivery based on the gelatinase-responsive strategy, Sal NPs was more effective and tolerable than free Sal.Conclusion: To the best of our knowledge, this is the first study to show that CCSC-targeted Sal NPs provide a potential approach to selectively target and efficiently eradicate CCSCs. This renders them a promising strategy to improve the therapeutic effect against cervical cancer.Keywords: nanoparticles, salinomycin, tumor-targeted delivery, cancer stem cells, epithelial interstitial transformation |
| first_indexed | 2024-12-14T13:59:10Z |
| format | Article |
| id | doaj.art-0b658a021cfa42d5b0ddbec2b0d66c36 |
| institution | Directory Open Access Journal |
| issn | 1178-2013 |
| language | English |
| last_indexed | 2024-12-14T13:59:10Z |
| publishDate | 2020-02-01 |
| publisher | Dove Medical Press |
| record_format | Article |
| series | International Journal of Nanomedicine |
| spelling | doaj.art-0b658a021cfa42d5b0ddbec2b0d66c362022-12-21T22:58:46ZengDove Medical PressInternational Journal of Nanomedicine1178-20132020-02-01Volume 151283129552086Enhanced and Prolonged Antitumor Effect of Salinomycin-Loaded Gelatinase-Responsive Nanoparticles via Targeted Drug Delivery and Inhibition of Cervical Cancer Stem CellsWang QLiu FWang LXie CWu PDu SZhou SSun ZLiu QYu LLiu BLi RQin Wang,1,* Fangcen Liu,2,* Lifeng Wang,1 Chen Xie,3 Puyuan Wu,1 Shiyao Du,1 Shujuan Zhou,1 Zhichen Sun,1 Qin Liu,1 Lixia Yu,1 Baorui Liu,1 Rutian Li1 1The Comprehensive Cancer Centre of Drum Tower Hospital, Medical School of Nanjing University, Clinical Cancer Institute of Nanjing University, Nanjing 210008, People’s Republic of China; 2The Comprehensive Cancer Centre, Nanjing Drum Tower Hospital, Clinical College of Nanjing Medical University, Nanjing, People’s Republic of China; 3Key Laboratory for Organic Electronics and Information Displays, Institute of Advanced Materials (IAM), Jiangsu National Synergetic Innovation Center for Advanced Materials (SICAM), Nanjing University of Posts & Telecommunications, Nanjing 210023, People’s Republic of China*These authors contributed equally to this workCorrespondence: Rutian Li; Baorui LiuThe Comprehensive Cancer Centre of Drum Tower Hospital, Medical School of Nanjing University, Clinical Cancer Institute of Nanjing University, 321 Zhongshan Road, Nanjing 210008, People’s Republic of ChinaTel +86-25-83107081Fax +86-25-83317016Email rutianli@nju.edu.cn; baoruiliu@nju.edu.cnBackground: Cervical cancer stem cells (CCSCs) represent a subpopulation of tumor cells that possess self-renewal capacity and numerous intrinsic mechanisms of resistance to conventional chemotherapy and radiotherapy. These cells play a crucial role in relapse and metastasis of cervical cancer. Therefore, eradication of CCSCs is the primary objective in cervical cancer therapy. Salinomycin (Sal) is an agent used for the elimination of cancer stem cells (CSCs); however, the occurrence of several side effects hinders its application. Nanoscale drug-delivery systems offer great promise for the diagnosis and treatment of tumors. These systems can be used to reduce the side effects of Sal and improve clinical benefit.Methods: Sal-loaded polyethylene glycol-peptide-polycaprolactone nanoparticles (Sal NPs) were fabricated under mild and non-toxic conditions. The real-time biodistribution of Sal NPs was investigated through non-invasive near-infrared fluorescent imaging. The efficacy of tumor growth inhibition by Sal NPs was evaluated using tumor xenografts in nude mice. Flow cytometry, immunohistochemistry, and Western blotting were used to detect the apoptosis of CSCs after treatment with Sal NPs. Immunohistochemistry and Western blotting were used to examine epithelial–mesenchymal transition (epithelial interstitial transformation) signal-related molecules.Results: Sal NPs exhibited antitumor efficacy against cervical cancers by inducing apoptosis of CCSCs and inhibiting the epithelial–mesenchymal transition pathway. Besides, tumor pieces resected from Sal NP-treated mice showed decreased reseeding ability and growth speed, further demonstrating the significant inhibitory ability of Sal NPs against CSCs. Moreover, owing to targeted delivery based on the gelatinase-responsive strategy, Sal NPs was more effective and tolerable than free Sal.Conclusion: To the best of our knowledge, this is the first study to show that CCSC-targeted Sal NPs provide a potential approach to selectively target and efficiently eradicate CCSCs. This renders them a promising strategy to improve the therapeutic effect against cervical cancer.Keywords: nanoparticles, salinomycin, tumor-targeted delivery, cancer stem cells, epithelial interstitial transformationhttps://www.dovepress.com/enhanced-and-prolonged-antitumor-effect-of-salinomycin-loaded-gelatina-peer-reviewed-article-IJNnanoparticlessalinomycintumor targeted deliverycancer stem cellsepithelial interstitial transformation; |
| spellingShingle | Wang Q Liu F Wang L Xie C Wu P Du S Zhou S Sun Z Liu Q Yu L Liu B Li R Enhanced and Prolonged Antitumor Effect of Salinomycin-Loaded Gelatinase-Responsive Nanoparticles via Targeted Drug Delivery and Inhibition of Cervical Cancer Stem Cells International Journal of Nanomedicine nanoparticles salinomycin tumor targeted delivery cancer stem cells epithelial interstitial transformation; |
| title | Enhanced and Prolonged Antitumor Effect of Salinomycin-Loaded Gelatinase-Responsive Nanoparticles via Targeted Drug Delivery and Inhibition of Cervical Cancer Stem Cells |
| title_full | Enhanced and Prolonged Antitumor Effect of Salinomycin-Loaded Gelatinase-Responsive Nanoparticles via Targeted Drug Delivery and Inhibition of Cervical Cancer Stem Cells |
| title_fullStr | Enhanced and Prolonged Antitumor Effect of Salinomycin-Loaded Gelatinase-Responsive Nanoparticles via Targeted Drug Delivery and Inhibition of Cervical Cancer Stem Cells |
| title_full_unstemmed | Enhanced and Prolonged Antitumor Effect of Salinomycin-Loaded Gelatinase-Responsive Nanoparticles via Targeted Drug Delivery and Inhibition of Cervical Cancer Stem Cells |
| title_short | Enhanced and Prolonged Antitumor Effect of Salinomycin-Loaded Gelatinase-Responsive Nanoparticles via Targeted Drug Delivery and Inhibition of Cervical Cancer Stem Cells |
| title_sort | enhanced and prolonged antitumor effect of salinomycin loaded gelatinase responsive nanoparticles via targeted drug delivery and inhibition of cervical cancer stem cells |
| topic | nanoparticles salinomycin tumor targeted delivery cancer stem cells epithelial interstitial transformation; |
| url | https://www.dovepress.com/enhanced-and-prolonged-antitumor-effect-of-salinomycin-loaded-gelatina-peer-reviewed-article-IJN |
| work_keys_str_mv | AT wangq enhancedandprolongedantitumoreffectofsalinomycinloadedgelatinaseresponsivenanoparticlesviatargeteddrugdeliveryandinhibitionofcervicalcancerstemcells AT liuf enhancedandprolongedantitumoreffectofsalinomycinloadedgelatinaseresponsivenanoparticlesviatargeteddrugdeliveryandinhibitionofcervicalcancerstemcells AT wangl enhancedandprolongedantitumoreffectofsalinomycinloadedgelatinaseresponsivenanoparticlesviatargeteddrugdeliveryandinhibitionofcervicalcancerstemcells AT xiec enhancedandprolongedantitumoreffectofsalinomycinloadedgelatinaseresponsivenanoparticlesviatargeteddrugdeliveryandinhibitionofcervicalcancerstemcells AT wup enhancedandprolongedantitumoreffectofsalinomycinloadedgelatinaseresponsivenanoparticlesviatargeteddrugdeliveryandinhibitionofcervicalcancerstemcells AT dus enhancedandprolongedantitumoreffectofsalinomycinloadedgelatinaseresponsivenanoparticlesviatargeteddrugdeliveryandinhibitionofcervicalcancerstemcells AT zhous enhancedandprolongedantitumoreffectofsalinomycinloadedgelatinaseresponsivenanoparticlesviatargeteddrugdeliveryandinhibitionofcervicalcancerstemcells AT sunz enhancedandprolongedantitumoreffectofsalinomycinloadedgelatinaseresponsivenanoparticlesviatargeteddrugdeliveryandinhibitionofcervicalcancerstemcells AT liuq enhancedandprolongedantitumoreffectofsalinomycinloadedgelatinaseresponsivenanoparticlesviatargeteddrugdeliveryandinhibitionofcervicalcancerstemcells AT yul enhancedandprolongedantitumoreffectofsalinomycinloadedgelatinaseresponsivenanoparticlesviatargeteddrugdeliveryandinhibitionofcervicalcancerstemcells AT liub enhancedandprolongedantitumoreffectofsalinomycinloadedgelatinaseresponsivenanoparticlesviatargeteddrugdeliveryandinhibitionofcervicalcancerstemcells AT lir enhancedandprolongedantitumoreffectofsalinomycinloadedgelatinaseresponsivenanoparticlesviatargeteddrugdeliveryandinhibitionofcervicalcancerstemcells |