Ultra-sensitive Nanoprobe Modified with Tumor Cell Membrane for UCL/MRI/PET Multimodality Precise Imaging of

Hanyi Fang1,2, Mengting Li1,2, Qingyao Liu1,2

  • 1Department of Nuclear Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, People's Republic of China.

Nano-Micro Letters
|June 17, 2021
PubMed

Insights

Researchers developed novel cancer cell membrane-coated upconversion nanoparticles (CCm-UCNPs) for improved triple-negative breast cancer (TNBC) diagnosis. This molecular imaging probe shows promise for differentiating TNBC subtypes and potential future therapeutic applications.

Area of Science:

  • Biomedical Engineering
  • Molecular Imaging
  • Nanotechnology

Background:

  • Triple-negative breast cancer (TNBC) presents significant diagnostic and therapeutic challenges due to the absence of key biomarkers.
  • Molecular imaging offers a promising avenue for TNBC diagnosis, with upconversion nanoparticles (UCNPs) emerging as potential probes.
  • Existing UCNPs require enhancements in tumor-targeting and biocompatibility for clinical utility.

Purpose of the Study:

  • To develop a novel molecular imaging probe for enhanced breast cancer molecular classification and TNBC diagnosis.
  • To improve the tumor-targeting ability and biocompatibility of upconversion nanoparticles (UCNPs).
  • To evaluate the tri-modality imaging capabilities (UCL/MRI/PET) of the novel probe in vivo.

Main Methods:

  • Fabrication of cancer cell membrane-coated upconversion nanoparticles (CCm-UCNPs) using biomimetic principles.
  • In vivo tri-modality imaging (UCL/MRI/PET) for molecular classification of breast cancer subtypes.
  • Differentiation of MDA-MB-231 (TNBC) from MCF-7 tumor models using the CCm-UCNPs probe.

Main Results:

  • The CCm-UCNPs probe demonstrated effective homologous-targeting and low immunogenicity.
  • Successful in vivo differentiation between MDA-MB-231 and MCF-7 tumor models was achieved.
  • The probe exhibited excellent performance in breast cancer molecular classification and TNBC diagnosis via tri-modality imaging.

Conclusions:

  • Biomimetic cancer cell membrane coating significantly enhances UCNP functionality for molecular imaging.
  • The developed CCm-UCNPs probe is highly effective for in vivo TNBC diagnosis and molecular subtyping.
  • This approach holds potential for future therapeutic modifications and broader clinical applications in oncology.

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