Phase-Change Assembling Nanostructures Synergistically Potentiate Tumor Radiosensitivity by Reducing the Stemness of Cancer Stem-Like Cells

Yuanfang Chen , Xueyin Hu , Ze Hu , Yuwei Yang , Changfen Bi , Guangyou Shi , Lumeng Zhang , Wenqing Xu , Shuqin Li , Luntao Liu

Exploration ›› 2026, Vol. 6 ›› Issue (1) : 20250179

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Exploration ›› 2026, Vol. 6 ›› Issue (1) :20250179 DOI: 10.1002/EXP.20250179
RESEARCH ARTICLE
Phase-Change Assembling Nanostructures Synergistically Potentiate Tumor Radiosensitivity by Reducing the Stemness of Cancer Stem-Like Cells
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Abstract

Cancer stem-like cells (CSCs) within deep tumors are a fundamental contributor to radiotherapy (RT) resistance due to their pronounced stemness resulting in unique unlimited self-renewal and differentiation capabilities. Alleviating hypoxic microenvironment of deep tumors to attenuate the stemness of CSCs remains a significant challenge, as the dense extracellular matrix (ECM) severely restricts oxygen diffusion into deep tumors. Herein, a nano-delivery particle (AMPM) is constructed to improve ECM permeability for deep tumor oxygen and radiosensitizer delivery. Natural fatty acid low-melting eutectic mixtures are employed as phase change materials (PCM) to encapsulate thermoresponsive self-assembled micelles, O2 pre-saturated perfluoropentane, and nitroimidazole sensitizers (metronidazole, MTZ), with the goal of enhancing RT. Under 808 nm light irradiation, PCM acts as a temperature-sensitive gatekeeper that undergoes solid-to-liquid phase transition under mild hyperthermic conditions (40°C), precisely controlling the release of MTZ and oxygen. Additionally, this design enhances the ECM permeability of the tumor, facilitating the delivery of oxygen and MTZ to deep-seated tumors. In TNBC (triple-negative breast cancer) mouse models, the combination of oxygen and MTZ effectively reverses radioresistance caused by hypoxic tumor microenvironment and CSCs, while significantly enhancing the efficacy of RT. Combination treatment with AMPM and RT (4 Gy) achieves a tumor inhibition rate of 91.2%, substantially surpassing high-dose RT alone (12 Gy, 52.1% inhibition). This study presents an innovative sensitization strategy with considerable clinical application potential for radiosensitization.

Keywords

cancer stem-like cells / radiosensitization / deep delivery / improved tumor hypoxia / photothermal effect

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Yuanfang Chen, Xueyin Hu, Ze Hu, Yuwei Yang, Changfen Bi, Guangyou Shi, Lumeng Zhang, Wenqing Xu, Shuqin Li, Luntao Liu. Phase-Change Assembling Nanostructures Synergistically Potentiate Tumor Radiosensitivity by Reducing the Stemness of Cancer Stem-Like Cells. Exploration, 2026, 6 (1) : 20250179 DOI:10.1002/EXP.20250179

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References

[1]

B. Jovanović, S. E. Church, K. M. Gorman, et al., “Integrative Multiomic Profiling of Triple-Negative Breast Cancer for Identifying Suitable Therapies,” Clinical Cancer Research 30 (2024): 4768–4779, https://doi.org/10.1158/1078-0432.CCR-23-1242.

[2]

R. A. Leon-Ferre and M. P. Goetz, “Advances in Systemic Therapies for Triple Negative Breast Cancer,” BMJ 381 (2023): e071674, https://doi.org/10.1136/bmj-2022-071674.

[3]

S. Zhu, Y. Wu, B. Song, et al., “Recent Advances in Targeted Strategies for Triple-Negative Breast Cancer,” Journal of Hematology & Oncology 16 (2023): 100, https://doi.org/10.1186/s13045-023-01497-3.

[4]

J. B. Schaubaecher, B. Smiljanov, F. Haring, et al., “Procoagulant Platelets Promote Immune Evasion in Triple-Negative Breast Cancer,” Blood 144 (2024): 216–226, https://doi.org/10.1182/blood.2023022928.

[5]

B. Liu, H. Zhou, L. Tan, K. T. H. Siu, and X.-Y. Guan, “Exploring Treatment Options in Cancer: Tumor Treatment Strategies,” Signal Transduction and Targeted Therapy 9 (2024): 175, https://doi.org/10.1038/s41392-024-01856-7.

[6]

I. Dagogo-Jack and A. T. Shaw, “Tumour Heterogeneity and Resistance to Cancer Therapies,” Nature Reviews Clinical oncology 15 (2018): 81–94, https://doi.org/10.1038/nrclinonc.2017.166.

[7]

F. Yang, “The Integration of Radiotherapy With Systemic Therapy in Advanced Triple-Negative Breast Cancer,” Critical Reviews in Oncology/Hematology 204 (2024): 104546.

[8]

G. Patel, A. Prince, and M. Harries, “Advanced Triple-Negative Breast Cancer,” Seminars in Oncology Nursing 40 (2024): 151548.

[9]

C. Sousa, M. Cruz, A. Neto, et al., “Neoadjuvant Radiotherapy in the Approach of Locally Advanced Breast Cancer,” ESMO Open 5 (2020): e000640.

[10]

M. Charpentier, S. Spada, S. J. Van Nest, and S. Demaria, “Radiation Therapy-Induced Remodeling of the Tumor Immune Microenvironment,” Seminars in Cancer Biology 86 (2022): 737–747, https://doi.org/10.1016/j.semcancer.2022.04.003.

[11]

T. Suwa, M. Kobayashi, J.-M. Nam, and H. Harada, “Tumor Microenvironment and Radioresistance,” Experimental & Molecular Medicine 53 (2021): 1029–1035, https://doi.org/10.1038/s12276-021-00640-9.

[12]

Y. Wu, Y. Song, R. Wang, and T. Wang, “Molecular Mechanisms of Tumor Resistance to Radiotherapy,” Molecular Cancer 22 (2023): 96, https://doi.org/10.1186/s12943-023-01801-2.

[13]

G. Dontu, M. Al-Hajj, W. M. Abdallah, M. F. Clarke, and M. S. Wicha, “Stem Cells in Normal Breast Development and Breast Cancer,” Cell Proliferation 36 (2003): 59–72, https://doi.org/10.1046/j.1365-2184.36.s.1.6.x.

[14]

F. R. Greten, “Tumour Stem-Cell Surprises,” Nature 543 (2017): 626–627, https://doi.org/10.1038/543626a.

[15]

M. Krause, A. Dubrovska, A. Linge, and M. Baumann, “Cancer Stem Cells: Radioresistance, Prediction of Radiotherapy Outcome and Specific Targets for Combined Treatments,” Advanced Drug Delivery Reviews 109 (2017): 63–73, https://doi.org/10.1016/j.addr.2016.02.002.

[16]

C. Peitzsch, A. Tyutyunnykova, K. Pantel, and A. Dubrovska, “Cancer Stem Cells: The Root of Tumor Recurrence and Metastases,” Seminars in Cancer Biology 44 (2017): 10–24, https://doi.org/10.1016/j.semcancer.2017.02.011.

[17]

X. Zhuo, R. Aishajiang, Y. Liang, et al., “Empowering Radiotherapy: Harnessing Nanomedicines to Enhance Radiation Response and Boost Antitumor Efficacy,” Coordination Chemistry Reviews 520 (2024): 216140, https://doi.org/10.1016/j.ccr.2024.216140.

[18]

G. Li, D. Wang, Y. Zhai, et al., “Glycometabolic Reprogramming-Induced XRCC1 Lactylation Confers Therapeutic Resistance in ALDH1A3-overexpressing Glioblastoma,” Cell Metabolism 36 (2024): 1696–1710.e10, https://doi.org/10.1016/j.cmet.2024.07.011.

[19]

D. C. Singleton, A. Macann, and W. R. Wilson, “Therapeutic Targeting of the Hypoxic Tumour Microenvironment,” Nature Reviews Clinical Oncology 18 (2021): 751–772, https://doi.org/10.1038/s41571-021-00539-4.

[20]

I. Telarovic, R. H. Wenger, and M. Pruschy, “Interfering with Tumor Hypoxia for Radiotherapy Optimization,” Journal of Experimental & Clinical Cancer Research 40 (2021): 197, https://doi.org/10.1186/s13046-021-02000-x.

[21]

H. Dou, Z. Luo, H. Wang, et al., “Tumor Microenvironment-Responsive Intelligent Nanoplatform With Oxygen Self-Supply for Synergistic Chemotherapy/Photodynamic Therapy/Photothermal Therapy against Hypoxic Tumors,” Chemical Engineering Journal 487 (2024): 150523, https://doi.org/10.1016/j.cej.2024.150523.

[22]

R. Kv, T.-I. Liu, I. L. Lu, et al., “Tumor Microenvironment-Responsive and Oxygen Self-Sufficient Oil Droplet Nanoparticles for Enhanced Photothermal/Photodynamic Combination Therapy Against Hypoxic Tumors,” Journal of Controlled Release 328 (2020): 87–99, https://doi.org/10.1016/j.jconrel.2020.08.038.

[23]

W. Wang, H. Zheng, J. Jiang, et al., “Engineering Micro Oxygen Factories to Slow Tumour Progression via Hyperoxic Microenvironments,” Nature Communications 13 (2022): 4495, https://doi.org/10.1038/s41467-022-32066-w.

[24]

Q. Wang, H. Cao, X. Hou, et al., “Cancer Stem-Like Cells-Oriented Surface Self-Assembly to Conquer Radioresistance,” Advanced Materials 35 (2023): 2302916, https://doi.org/10.1002/adma.202302916.

[25]

A. Choudhury, M. A. Cady, C.-H. G. Lucas, et al., “Perivascular NOTCH3+ Stem Cells Drive Meningioma Tumorigenesis and Resistance to Radiotherapy,” Cancer Discovery 14 (2024): 1823–1837.

[26]

T. Sun, B. Liu, Y. Cao, Y. Li, L. Cai, and W. Yang, “AMPK-Mediated CD47 H3K4 Methylation Promotes Phagocytosis Evasion of Glioma Stem Cells Post-Radiotherapy,” Cancer Letters 583 (2024): 216605, https://doi.org/10.1016/j.canlet.2023.216605.

[27]

B. C. Prager, Q. Xie, S. Bao, and J. N. Rich, “Cancer Stem Cells: The Architects of the Tumor Ecosystem,” Cell Stem Cell 24 (2019): 41–53, https://doi.org/10.1016/j.stem.2018.12.009.

[28]

M. Tutter, C. Schug, K. A. Schmohl, et al., “Regional Hyperthermia Enhances Mesenchymal Stem Cell Recruitment to Tumor Stroma: Implications for Mesenchymal Stem Cell-Based Tumor Therapy,” Molecular Therapy 29 (2021): 788–803, https://doi.org/10.1016/j.ymthe.2020.10.009.

[29]

X. Wu, Y. Zhu, W. Huang, et al., “Hyperbaric Oxygen Potentiates Doxil Antitumor Efficacy by Promoting Tumor Penetration and Sensitizing Cancer Cells,” Advancement of Science 5 (2018): 1700859, https://doi.org/10.1002/advs.201700859.

[30]

J. Gao, H. Qin, F. Wang, et al., “Hyperthermia-Triggered Biomimetic Bubble Nanomachines,” Nature Communications 14 (2023): 4867, https://doi.org/10.1038/s41467-023-40474-9.

[31]

S. He, X. Gou, S. Zhang, et al., “Nanodelivery Systems as a Novel Strategy to Overcome Treatment Failure of Cancer,” Small Methods 8 (2024): 2301127, https://doi.org/10.1002/smtd.202301127.

[32]

Y. Xia, S. Fu, Q. Ma, Y. Liu, and N. Zhang, “Application of Nano-Delivery Systems in Lymph Nodes for Tumor Immunotherapy,” Nano-Micro Letters 15 (2023): 145, https://doi.org/10.1007/s40820-023-01125-2.

[33]

M. I. Priester and T. L. M. ten Hagen, “Image-Guided Drug Delivery in Nanosystem-Based Cancer Therapies,” Advanced Drug Delivery Reviews 192 (2023): 114621, https://doi.org/10.1016/j.addr.2022.114621.

[34]

Z. Cao, J. Liu, and X. Yang, “Deformable Nanocarriers for Enhanced Drug Delivery and Cancer Therapy,” Exploration 4 (2024): 20230037, https://doi.org/10.1002/EXP.20230037.

[35]

A. D. Theocharis, S. S. Skandalis, C. Gialeli, and N. K. Karamanos, “Extracellular Matrix Structure,” Advanced Drug Delivery Reviews 97 (2016): 4–27.

[36]

Y. X. Zhu, H. R. Jia, Y. W. Jiang, et al., “A Red Blood Cell-Derived Bionic Microrobot Capable of Hierarchically Adapting to Five Critical Stages in Systemic Drug Delivery,” Exploration 4 (2024): 20230105, https://doi.org/10.1002/EXP.20230105.

[37]

J. Insua-Rodríguez and T. Oskarsson, “The Extracellular Matrix in Breast Cancer,” Advanced Drug Delivery Reviews 97 (2016): 41–55, https://doi.org/10.1016/j.addr.2015.12.017.

[38]

M. Li, Y. Zhang, Q. Zhang, and J. Li, “Tumor Extracellular Matrix Modulating Strategies for Enhanced Antitumor Therapy of Nanomedicines,” Mater Today Bio 16 (2022): 100364, https://doi.org/10.1016/j.mtbio.2022.100364.

[39]

Q. Zhou, S. Shao, J. Wang, et al., “Enzyme-Activatable Polymer–Drug Conjugate Augments Tumour Penetration and Treatment Efficacy,” Nature Nanotechnology 14 (2019): 799–809, https://doi.org/10.1038/s41565-019-0485-z.

[40]

Y. Shen, Y. Zou, B. Bie, and Y. Lv, “Hierarchically Released Liquid Metal Nanoparticles for Mild Photothermal Therapy/Chemotherapy of Breast Cancer Bone Metastases via Remodeling Tumor Stromal Microenvironment,” Advanced Healthcare Materials 12 (2023): 2301080, https://doi.org/10.1002/adhm.202301080.

[41]

M. Zhan, X. Yu, W. Zhao, et al., “Extracellular Matrix-Degrading STING Nanoagonists for Mild NIR-II Photothermal-Augmented Chemodynamic-Immunotherapy,” Journal of Nanbiotechnology 20 (2022): 23, https://doi.org/10.1186/s12951-021-01226-3.

[42]

L. P. Liew, A. Shome, W. W. Wong, et al., “Design, Synthesis and Anticancer Evaluation of Nitroimidazole Radiosensitisers,” Molecules (Basel, Switzerland) 28 (2023): 4457, https://doi.org/10.3390/molecules28114457.

[43]

C. Li, Y. Zhang, Z. Li, et al., “Light-Responsive Biodegradable Nanorattles for Cancer Theranostics,” Advanced Materials 30 (2018): 1706150, https://doi.org/10.1002/adma.201706150.

[44]

X. Wang, Y. Mao, C. Sun, Q. Zhao, Y. Gao, and S. Wang, “A Versatile Gas-Generator Promoting Drug Release and Oxygen Replenishment for Amplifying Photodynamic-Chemotherapy Synergetic Anti-Tumor Effects,” Biomaterials 276 (2021): 120985, https://doi.org/10.1016/j.biomaterials.2021.120985.

[45]

X. Liang, W. Chen, C. Wang, et al., “A Mesoporous Theranostic Platform for Ultrasound and Photoacoustic Dual Imaging-Guided Photothermal and Enhanced Starvation Therapy for Cancer,” Acta Biomaterialia 183 (2024): 264–277, https://doi.org/10.1016/j.actbio.2024.05.040.

[46]

M. W. Luczak and A. Zhitkovich, “Monoubiquitinated γ-H2AX: Abundant Product and Specific Biomarker for Non-Apoptotic DNA Double-Strand Breaks,” Toxicology and Applied Pharmacology 355 (2018): 238–246, https://doi.org/10.1016/j.taap.2018.07.007.

[47]

V. Raavi, V. Perumal, and S. F. D. Paul, “Potential Application of γ-H2AX as a Biodosimetry Tool for Radiation Triage,” Mutation Research Reviews in Mutation Research 787 (2021): 108350.

[48]

A. Collins, P. Møller, G. Gajski, et al., “Measuring DNA Modifications With the Comet Assay: A Compendium of Protocols,” Nature Protocols 18 (2023): 929–989, https://doi.org/10.1038/s41596-022-00754-y.

[49]

E. Bivehed, B. Hellman, L. Wenson, B. Stenerlöw, O. Söderberg, and J. Heldin, “Visualizing DNA Single- and Double-Strand Breaks in the Flash Comet Assay by DNA Polymerase-Assisted End-Labelling,” Nucleic Acids Research 52 (2024): e22, https://doi.org/10.1093/nar/gkae009.

[50]

S. Basu, Y. Dong, R. Kumar, C. Jeter, and D. G. Tang, “Slow-Cycling (Dormant) Cancer Cells in Therapy Resistance, Cancer Relapse and Metastasis,” Seminars in Cancer Biology 78 (2022): 90–103, https://doi.org/10.1016/j.semcancer.2021.04.021.

[51]

L. Ma, B. Qiu, J. Zhang, et al., “Survival and Prognostic Factors of Non-Small Cell Lung Cancer Patients with Postoperative Locoregional Recurrence Treated With Radical Radiotherapy,” Chinese Journal of Cancer 36 (2017): 93, https://doi.org/10.1186/s40880-017-0261-0.

[52]

M. Rafat, T. A. Aguilera, M. Vilalta, et al., “Macrophages Promote Circulating Tumor Cell–Mediated Local Recurrence Following Radiotherapy in Immunosuppressed Patients,” Cancer Research 78 (2018): 4241–4252, https://doi.org/10.1158/0008-5472.CAN-17-3623.

[53]

D. Bayik and J. D. Lathia, “Cancer Stem Cell-Immune Cell Crosstalk in Tumour Progression,” Nature Reviews Cancer 21 (2021): 526–536.

[54]

S. Shen, X. Xu, S. Lin, et al., “A Nanotherapeutic Strategy to Overcome Chemotherapeutic Resistance of Cancer Stem-Like Cells,” Nature Nanotechnology 16 (2021): 104–113, https://doi.org/10.1038/s41565-020-00793-0.

[55]

Y. Xiong, Z. Yong, C. Xu, et al., “Hyperbaric Oxygen Activates Enzyme-Driven Cascade Reactions for Cooperative Cancer Therapy and Cancer Stem Cells Elimination,” Advancement of Science 10 (2023): 2301278, https://doi.org/10.1002/advs.202301278.

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