Cryo-Shocked Cancer Cell Biomimetic Carriers Enhance Tumor-Targeted Doxorubicin Delivery in Triple-Negative Breast Cancer
Source abstract
Abstract
Triple-negative breast cancer (TNBC) is an aggressive subtype with no defined therapeutic targets and high intratumoral heterogeneity. These features severely limit the efficacy of conventional chemotherapy. In this study, a biomimetic drug delivery platform was developed by cryo-shock treatment of 4T1 tumor cells (CS cells) to generate nonviable, structurally intact carriers, which were subsequently loaded with doxorubicin (DOX/CS cells). DOX/CS cells preserve native membrane proteins and chemotactic properties, facilitating enhanced tumor homing and tissue penetration without the risks associated with live-cell vectors. In vitro and in vivo analyses demonstrated that DOX/CS cells exhibit improved tumor-specific uptake, sustained drug release, and markedly enhanced antitumor activity compared to free DOX. Furthermore, systemic administration of DOX/CS cells achieved favorable biodistribution with minimal off-target toxicity. These findings indicate that cryo-shocked cancer cells offer a simplified yet potent platform for targeted drug delivery, offering a promising strategy for the safe and effective treatment of TNBC.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Nanoplatforms for cancer theranostics · Nanoparticle-Based Drug Delivery · Endoplasmic Reticulum Stress and Disease
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Pharmaceutical Sciences
Wenzhou Medical University
Research Institute of Pharmaceutical Sciences, College of Pharmacy
Chonnam National University
Cixi Biomedical Research Institute
Funding
Natural Science Foundation of Zhejiang Province · the Summit Advancement Disciplines of Zhejiang Province (Wenzhou Medical University - Pharmaceutics)
References (29)
Show source-provided references
1. 10.1002/advs.20230285710.1002/advs.202302857 ↗
2. 10.1016/j.mtbio.2024.10135810.1016/j.mtbio.2024.101358 ↗
3. 10.1016/j.jconrel.2024.05.02010.1016/j.jconrel.2024.05.020 ↗
4. 10.1002/adhm.20240418410.1002/adhm.202404184 ↗
5. 10.1038/s41392-023-01703-110.1038/s41392-023-01703-1 ↗
6. 10.1002/adhm.20240021910.1002/adhm.202400219 ↗
7. 10.1021/acs.molpharmaceut.3c0000910.1021/acs.molpharmaceut.3c00009 ↗
8. 10.1016/j.apsb.2019.01.01110.1016/j.apsb.2019.01.011 ↗
9. 10.1021/acsnano.4c0707410.1021/acsnano.4c07074 ↗
10. 10.1016/j.mtbio.2025.10159710.1016/j.mtbio.2025.101597 ↗
11. 10.1016/j.jconrel.2023.07.06310.1016/j.jconrel.2023.07.063 ↗
12. 10.1016/j.bioactmat.2022.08.02810.1016/j.bioactmat.2022.08.028 ↗
13. 10.1016/j.biomaterials.2022.12172210.1016/j.biomaterials.2022.121722 ↗
14. 10.1002/smll.20240719110.1002/smll.202407191 ↗
15. 10.1021/acsnano.4c0565710.1021/acsnano.4c05657 ↗
16. 10.1007/s11010-022-04459-410.1007/s11010-022-04459-4 ↗
17. 10.1186/s12951-019-0526-710.1186/s12951-019-0526-7 ↗
18. 10.1038/s41467-019-11718-410.1038/s41467-019-11718-4 ↗
19. 10.1016/j.jconrel.2024.07.00910.1016/j.jconrel.2024.07.009 ↗
20. 10.1002/adma.20231221910.1002/adma.202312219 ↗
21. 10.1002/adhm.20240012510.1002/adhm.202400125 ↗
22. 10.1126/sciadv.adk826410.1126/sciadv.adk8264 ↗
23. 10.1021/acsnano.2c1186510.1021/acsnano.2c11865 ↗
24. 10.7150/ijbs.6843810.7150/ijbs.68438 ↗
25. 10.1016/j.ijpharm.2022.12177510.1016/j.ijpharm.2022.121775 ↗
26. 10.1002/adma.20240851110.1002/adma.202408511 ↗
27. 10.1002/smll.20230927910.1002/smll.202309279 ↗
28. 10.1021/acsnano.3c0019510.1021/acsnano.3c00195 ↗
29. 10.1136/bmj-2022-07167410.1136/bmj-2022-071674 ↗