Nanodelivery Vectors Veiled in Natural Killer Cell Membranes: Enhancing Colorectal Cancer Therapy through Synergistic Starvation and Chemotherapy
Source abstract
Abstract
The application of oxaliplatin (L–OHP) in colorectal cancer chemotherapy has attracted considerable attention. However, its toxic side effects have hindered its clinical use. This study aims to develop a nanoparticle-based drug delivery system using L–OHP as the therapeutic agent, designated as NGMP. NGMP is designed to possess targeting capability, pH responsiveness, and MR imaging functionality. The ultimated goal of this system is to achieve a synergistic effect in colorectal cancer treatment by combining starvation therapy, chemodynamic therapy, and chemotherapy. NGMP delivers Manganese dioxide (MnO 2 ) into tumor cells, where the acidic and glutathione (GSH)-rich tumor microenvironment (TME) rapidly triggers its degradation. This reaction liberates L–OHP, glucose oxidase (GOX), and Mn 2+ ions. The released Mn 2+ catalyzes a Fenton-like reaction with endogenous hydrogen peroxide (H 2 O 2 ), producing abundant reactive oxygen species (ROS) and driving oxidative damage–induced cell death. Concurrent GSH depletion sensitizes tumor cells to ROS and chemotherapeutic agents, thereby amplifying cytotoxicity. GOX-mediated glucose consumption induces metabolic starvation (starvation therapy), simultaneously replenishes H 2 O 2, and lowers the local pH, thereby establishing a positive feedback loop that synergistically enhances both starvation therapy and chemodynamic therapy. Collectively, these effects result in self-amplifying, multimodal tumor eradication. NGMP is cloaked with natural killer cell membranes (NKm) to enhance tumor specificity and modulate immune responses. This coating enables immune evasion, facilitates active tumor targeting, and promotes immunotherapeutic synergy. Compared with free L–OHP, NGMP demonstrates superior antitumor efficacy, greater biocompatibility, and integrated diagnostic functionality. These combined features position NGMP as a potential theranostic platform for colorectal cancer.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Nanoplatforms for cancer theranostics · Nanoparticle-Based Drug Delivery · Sulfur Compounds in Biology
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Gastrointestinal Surgery, Zhongshan Hospital of Xiamen University, No.201-209, Hubin South Road, Xiamen 361004, Fujian, People’s Republic of China
Medical College of Guangxi University
Fujian Maternity and Child Health Hospital, 18 Daoshan Road, Fuzhou 350001, Fujian, People’s Republic of China
Institute of Gastrointestinal Oncology, Medical College of Xiamen University, No. 201-209, Hubin South Road, Xiamen 361004, Fujian, People’s Republic of China
Funding
Fujian Provincial Department of Science and Technology
References (31)
Show source-provided references
1. 10.1038/d41573-020-00202-010.1038/d41573-020-00202-0 ↗
2. 10.1093/clinchem/hvad20210.1093/clinchem/hvad202 ↗
3. Global, regional, and national burden of colorectal cancer and its risk factors, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019 Lancet Gastroenterol. Hepatol. 2022; Vol. 7 7, pp 627–647.
4. Liuchuang Z. · J. Colorectal Anal Surgery · 2025 · 31 · 179
5. 10.1016/S0140-6736(19)32319-010.1016/S0140-6736(19)32319-0 ↗
6. 10.1001/jama.2018.1932310.1001/jama.2018.19323 ↗
7. 10.1016/j.drup.2024.10115210.1016/j.drup.2024.101152 ↗
8. 10.1371/journal.pone.018625010.1371/journal.pone.0186250 ↗
9. 10.1016/j.biomaterials.2020.12034610.1016/j.biomaterials.2020.120346 ↗
10. 10.1016/j.actbio.2022.05.02410.1016/j.actbio.2022.05.024 ↗
11. 10.1021/jacs.8b0871410.1021/jacs.8b08714 ↗
12. 10.1016/j.pdpdt.2021.10260510.1016/j.pdpdt.2021.102605 ↗
13. 10.1002/adma.20200689210.1002/adma.202006892 ↗
14. 10.1039/D1NA00697E10.1039/D1NA00697E ↗
15. 10.1016/j.jconrel.2025.02.07610.1016/j.jconrel.2025.02.076 ↗
16. 10.1016/j.actbio.2022.01.01910.1016/j.actbio.2022.01.019 ↗
17. 10.1021/acsnano.9b0583610.1021/acsnano.9b05836 ↗
18. 10.1016/j.cclet.2024.11077010.1016/j.cclet.2024.110770 ↗
19. 10.1002/advs.20210574710.1002/advs.202105747 ↗
20. 10.1016/j.biomaterials.2025.12331910.1016/j.biomaterials.2025.123319 ↗
21. 10.1016/j.biomaterials.2025.12335410.1016/j.biomaterials.2025.123354 ↗
22. 10.1016/j.biomaterials.2024.12292110.1016/j.biomaterials.2024.122921 ↗
23. 10.3390/pharmaceutics1402030410.3390/pharmaceutics14020304 ↗
24. 10.1016/j.jcis.2023.04.04910.1016/j.jcis.2023.04.049 ↗
25. 10.1016/j.actbio.2021.03.04810.1016/j.actbio.2021.03.048 ↗
26. 10.1039/D0CC02782K10.1039/D0CC02782K ↗
27. 10.1186/s12951-019-0513-z10.1186/s12951-019-0513-z ↗
28. 10.1021/acs.accounts.9b0007910.1021/acs.accounts.9b00079 ↗
29. 10.1016/j.biomaterials.2018.01.01810.1016/j.biomaterials.2018.01.018 ↗
30. 10.3389/fimmu.2017.0121410.3389/fimmu.2017.01214 ↗
31. 10.1016/j.aca.2020.09.01010.1016/j.aca.2020.09.010 ↗