Cancer cell membrane-coated siRNA-Decorated Au/MnO2 nanosensitizers for synergistically enhanced radio-immunotherapy of breast cancer
Open accessAbstract
Radiotherapy plays a critical role in the clinical treatment of breast cancer. However, the efficacy of traditional X-ray radiotherapy is greatly limited by its low tumor specificity and treatment tolerance mediated by the tumor microenvironment. Herein, we proposed a novel nano-radiotherapy sensitization strategy to design and construct a cancer cell membrane-coated siRNA-decorated Au/MnO 2 nanosensitizer (R&F@Au/MnO 2 -CM) to synergistically enhance radio-immunotherapy for breast cancer. In the integrated nanosensitizer, the cancer cell membrane (CM) derived from 4T1 breast cancer cells is utilized for targeted functionality, while Au/MnO 2 is designed to improve X-ray absorption and alleviate tumor hypoxia. Additionally, PD-L1 siRNA (R) is used to downregulate PD-L1 expression in tumor cells. In an in situ mouse model of 4T1 breast cancer, R&F@Au/MnO 2 -CM demonstrated accurate tumor identification via CM-mediated homologous targeting after intravenous injection, which was monitored in real-time through NIR-II fluorescence imaging of NIR-935 (F). Subsequently, the radiotherapy sensitivity was achieved due to the strong radiation absorption properties and oxygen generation through catalysis of Au/MnO 2 upon X-ray irradiation. Furthermore, the immunosuppressive microenvironment of the tumor is improved by downregulating PD-L1, enhancing synergistic anti-tumor effect. Our findings demonstrate a promising approach for tumor treatment by combining targeted enhanced radiotherapy with immune activation.
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Biomimetic strategies, including cell membrane-coated nanoparticles, were reported to enhance circulation time and immune evasion.
“Biomimetic strategies, including cell membrane-coated nanoparticles, were reported to enhance circulation time and immune evasion [34,44,50,56].”
From Nanoparticle-Mediated Radiosensitization in Breast Cancer: A Systematic Review of Preclinical Evidence and Translational Challenges (2026) · cites this paper as [56]
The Results and discussion section (‘In vivo homologous targeting and anti-tumor efficiency’; page unavailable) reports a 3.79-hour blood half-life for the cell membrane-coated nanosensitizer and calls its circulation characteristics favorable. It does not show that membrane coating increased circulation time relative to an uncoated comparator or that the nanoparticles evaded immune clearance. Its discussion of immune evasion concerns tumor-cell PD-L1, not nanoparticle immune evasion. (LLM, conf=0.82)
Experimental — accuracy not yet measuredImmune-modulating strategies, including checkpoint-related approaches, were described in combination with radiotherapy in selected nanoplatforms.
“Immune-modulating strategies, including checkpoint-related approaches, were described in combination with radiotherapy in selected nanoplatforms [17,21,23,26,39,56].”
From Nanoparticle-Mediated Radiosensitization in Breast Cancer: A Systematic Review of Preclinical Evidence and Translational Challenges (2026) · cites this paper as [56]
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- Authors
- Wang, D., Lin, S., Li, T., Yang, X., Zhong, X., Chen, Q., Jiang, G., & Li, C.
- Affiliations
- Chinese Academy of Sciences (CN)
- Second Affiliated Hospital of Soochow University (CN)
- University of Science and Technology of China (CN)
- Corresponding author
- Jiang, Guoqin
- Li, Chunyan
- Venue
- Materials Today Bio
- Publisher
- Elsevier BV
- Published
- 2024-12
- Volume
- 29
- Pages
- 101275
- ISSN
- 2590-0064 (ISSN-L)
- PMC
- PMC11471673
- OpenAlex
- W4402878349
- Cited by
- 18
- References
- 67
- Citations by year
- 2026: 6 · 2025: 12
- FWCI
- 1.98
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Materials Today Bio (publishedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Key Research and Development Program of China Stem Cell and Translational Research
- Topics
- Physical Sciences › Engineering › Biomedical Engineering › Nanoplatforms for cancer theranostics
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Radiation Therapy and Dosimetry
- Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
- Keywords
- breast cancer, radioimmunotherapy, cancer cell membrane coating, tumor hypoxia, X-ray absorption, NIR-II fluorescence imaging, tumor microenvironment, 4T1 cells, targeted drug delivery, oxygen production
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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