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Magnetically Stimulated Integrin Binding Alters Cell Polarity and Affects Epithelial–Mesenchymal Plasticity in Metastatic Cancer Cells
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    Biological and Medical Applications of Materials and Interfaces

    Magnetically Stimulated Integrin Binding Alters Cell Polarity and Affects Epithelial–Mesenchymal Plasticity in Metastatic Cancer Cells
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    • Yu Jin Kim
      Yu Jin Kim
      Institute for High Technology Materials and Devices, Korea University, Seoul 02841, Korea
      More by Yu Jin Kim
    • Dae Beom Lee
      Dae Beom Lee
      Department of Materials Science and Engineering, Korea University, Seoul 02841, Korea
      More by Dae Beom Lee
    • Eunjin Jeong
      Eunjin Jeong
      Department of Materials Science and Engineering, Korea University, Seoul 02841, Korea
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    • Joo Yeong Jeon
      Joo Yeong Jeon
      Seoul Center, Korea Basic Science Institute, Seoul 03759, Korea
    • Hee-Dae Kim
      Hee-Dae Kim
      Department of Basic Medical Sciences, University of Arizona College of Medicine─Phoenix, Phoenix, Arizona 85004, United States
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    • Heemin Kang
      Heemin Kang
      Department of Materials Science and Engineering, Korea University, Seoul 02841, Korea
      More by Heemin Kang
    • Young Keun Kim*
      Young Keun Kim
      Institute for High Technology Materials and Devices, Korea University, Seoul 02841, Korea
      Department of Materials Science and Engineering, Korea University, Seoul 02841, Korea
      *Email: [email protected]
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    ACS Applied Materials & Interfaces

    Cite this: ACS Appl. Mater. Interfaces 2024, 16, 7, 8365–8377
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    https://doi.org/10.1021/acsami.3c16720
    Published February 6, 2024
    Copyright © 2024 American Chemical Society

    Abstract

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    Inorganic nanoparticles (NPs) have been widely recognized for their stability and biocompatibility, leading to their widespread use in biomedical applications. Our study introduces a novel approach that harnesses inorganic magnetic nanoparticles (MNPs) to stimulate apical–basal polarity and induce epithelial traits in cancer cells, targeting the hybrid epithelial/mesenchymal (E/M) state often linked to metastasis. We employed mesocrystalline iron oxide MNPs to apply an external magnetic field, disrupting normal cell polarity and simulating an artificial cellular environment. These led to noticeable changes in the cell shape and function, signaling a shift toward the hybrid E/M state. Our research suggests that apical–basal stimulation in cells through MNPs can effectively modulate key cellular markers associated with both epithelial and mesenchymal states without compromising the structural properties typical of mesenchymal cells. These insights advance our understanding of how cells respond to physical cues and pave the way for novel cancer treatment strategies. We anticipate that further research and validation will be instrumental in exploring the full potential of these findings in clinical applications, ensuring their safety and efficacy.

    Copyright © 2024 American Chemical Society

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    Supporting Information

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    The Supporting Information is available free of charge at https://pubs.acs.org/doi/10.1021/acsami.3c16720.

    • Detailed information on materials characterizations and additional experimental processes, including the characterization of nanoparticles, surface modifications, Western blot, AFM image, and immunofluorescence images; Figures S1–S12 (PDF)

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    Cited By

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    This article is cited by 1 publications.

    1. Zhiyu Ding, Junjie Huang, Yijun Ren, Ning Tang, Xin Luo, Huancheng Zhu, Xu Cao, Ming Zhao, Song Wu. 3D bioprinted advanced cartilage organoids with engineered magnetic nanoparticles polarized-BMSCs/alginate/gelatin for cartilage tissue regeneration. Nano Research 2025, 18 (2) , 94907084. https://doi.org/10.26599/NR.2025.94907084

    ACS Applied Materials & Interfaces

    Cite this: ACS Appl. Mater. Interfaces 2024, 16, 7, 8365–8377
    Click to copy citationCitation copied!
    https://doi.org/10.1021/acsami.3c16720
    Published February 6, 2024
    Copyright © 2024 American Chemical Society

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