A cisplatin prodrug-based self-assembling ozone delivery nanosystem sensitizes radiotherapy in triple-negative breast cancer.
10.1016/j.apsb.2025.03.020
- Author:
Tianyue XU
1
;
Dan ZHENG
1
;
Meixu CHEN
1
;
Linlin SONG
1
;
Zhihui LIU
1
;
Yan CHENG
2
;
Yujie ZHAO
1
;
Liwen HUANG
1
;
Yixuan LI
1
;
Zhankun YANG
3
;
Cong LI
4
;
Biao DONG
5
;
Jing JING
1
;
Hubing SHI
1
Author Information
1. Institute of Breast Health Medicine, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University and Collaborative Innovation Center, Chengdu 610041, China.
2. Cancer Center, Breast Center, West China Hospital, Sichuan University, Chengdu 610041, China.
3. College of Chemical Engineering, Shijiazhuang University, Shijiazhuang 050035, China.
4. Core Facilities of West China Hospital, Sichuan University, Chengdu 610041, China.
5. National Clinical Research Center for Geriatrics and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu 610041, China.
- Publication Type:Journal Article
- Keywords:
Cisplatin;
Controlled-release system;
Immunogenic cell death;
Ozone;
Prodrug;
Radiotherapy;
Reactive oxygen species;
Triple-negative breast cancer
- From:
Acta Pharmaceutica Sinica B
2025;15(5):2703-2722
- CountryChina
- Language:English
-
Abstract:
Lacking therapeutic targets highlights the crucial roles of chemotherapy and radiotherapy in the clinical management of triple-negative breast cancer (TNBC). To relieve the side effects of the chemoradiotherapy combination regimen, we design and develop a self-assembled micelle nanosystem consisting of perfluorocarbon chain-modified cisplatin prodrug. By incorporating perfluorodecalin, this nanosystem can effectively carry ozone and promote irradiation-derived reactive oxygen species (ROS) production. By leveraging the perfluorocarbon sidechain, the nanosystem exhibits efficient internalization by TNBC cells and effectively escapes from lysosomal entrapment. Under X-ray irradiation, ozone-generated ROS disrupts the intracellular redox balance, thereby facilitating the release of cisplatin in a reduction-responsive manner mediated by reduced glutathione. Moreover, oxygen derived from ozone decomposition enhances the efficacy of radiotherapy by alleviating tumor hypoxia. Notably, the combination of irradiation with ozone-loaded cisplatin prodrug nano system synergistically prompts antitumor efficacy and reduces cellular/systemic toxicity in vitro and in vivo. Furthermore, the combo regimen remodels the tumor microenvironment into an immune-favored state by triggering immunogenic cell death and relieving hypoxia, which provides a promising foundation for a combination regimen of immunotherapy. In conclusion, our nanosystem presents a novel strategy for integrating chemotherapy and radiotherapy to optimize the efficacy and safety of TNBC clinical treatment.
