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A Cascade Recognition of Activatable Probe for Fluorescence Navigation Glioblastoma Surgery: Overcoming Blood-Brain
Xinru An1, Yu Guo2,3, Yongning Bian1
1Department of Chemistry, Beijing University of Technology, Beijing, P. R. China.
Abstract:
Precise imaging and complete resection of glioblastoma (GBM) remain critically challenging due to two major obstacles: the inefficient delivery of probes across the blood-brain barrier (BBB) and the lack of tumor-specific activation, leading to poor contrast and inadequate tumor margin delineation. To address these challenges, we developed ANG-hCy-MC, a cascade recognition of activatable probe designed for high-fidelity visualization of GBM. This probe leverages Angiopep-2-mediated targeting of LRP1 receptors to facilitate efficient BBB crossing, followed by a cascaded activation process triggered specifically by the tumor-associated enzymes cathepsin B (Cat B) and monoamine oxidase (MAO). This dual-enzyme cascade mechanism ensures ultra-selective fluorescence turn-on exclusively within tumor cells, thereby eliminating off-target signals and providing exceptional tumor-to-normal tissue contrast, enabling the precise navigation and resection of orthotopic glioblastoma in live mice. Notably, in ex vivo human GBM specimens, ANG-hCy-MC achieved a remarkable tumor-to-normal fluorescence ratio of 7.83 at the invasive edge, enabling clear identification of even single infiltrating tumor cells. This probe allows real-time, high-contrast intraoperative guidance with unprecedented resolution, offering a powerful and clinically translatable strategy for achieving complete tumor resection and improved patient outcomes in GBM surgery.
Insights
A new activatable probe, ANG-hCy-MC, improves glioblastoma (GBM) imaging by crossing the blood-brain barrier and activating via tumor enzymes. This enhances tumor visualization for precise surgical resection.
Area of Science:
- Neuro-oncology
- Molecular Imaging
- Biotechnology
Background:
- Glioblastoma (GBM) resection is limited by poor contrast and blood-brain barrier (BBB) penetration of imaging probes.
- Current probes lack tumor-specific activation, leading to inadequate delineation of tumor margins.
Purpose of the Study:
- To develop a novel activatable probe for high-fidelity visualization and precise resection of GBM.
- To overcome challenges of BBB delivery and achieve tumor-specific probe activation.
Main Methods:
- Development of ANG-hCy-MC, a probe utilizing Angiopep-2 for LRP1 receptor targeting across the BBB.
- Cascade activation triggered by tumor-associated enzymes: cathepsin B (Cat B) and monoamine oxidase (MAO).
- Evaluation in orthotopic glioblastoma mouse models and ex vivo human GBM specimens.
Main Results:
- ANG-hCy-MC demonstrated efficient BBB crossing and selective fluorescence turn-on within tumor cells.
- Achieved exceptional tumor-to-normal tissue contrast, enabling precise navigation in live mice.
- Ex vivo human GBM specimens showed a 7.83 tumor-to-normal fluorescence ratio at the invasive edge, identifying infiltrating cells.
Conclusions:
- ANG-hCy-MC offers real-time, high-contrast intraoperative guidance for GBM surgery.
- The probe enables precise identification of tumor margins and infiltrating cells.
- This strategy is clinically translatable for improving GBM resection and patient outcomes.
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