# Targeting Gliomas with Beta-Amyloid-Specific Dyes: A Novel Approach for In Vivo Staining and Potential Therapeutic Applications

**Authors:** Lilia Kucheryavykh, Jescelica Ortiz Rivera, Boris Ermolinsky, Vassiliy Tsytsarev, Lynnette Cary, Janaina Alves, Adriana Reyes, Noelis de la Cruz-Rivera, Kevin Rosa Gonzalez, Felix Narvaez Irizarry, Tyrel R. Porter, Mikhail Inyushin

PMC · DOI: 10.3390/ijms262110450 · International Journal of Molecular Sciences · 2025-10-28

## TL;DR

This study explores using beta-amyloid-specific dyes to stain gliomas in the brain, offering new ways to visualize and potentially treat these tumors.

## Contribution

The novel use of beta-amyloid-specific dyes for glioma staining and potential targeted therapy delivery is introduced.

## Key findings

- Brilliant Blue G and BAP-1 selectively stain gliomas in mouse models.
- The dyes provide clear contrast between glioma and normal brain tissue.
- The dyes show potential for glioma visualization and targeted therapeutic applications.

## Abstract

Gliomas, the most common primary brain tumors, present significant diagnostic and treatment challenges due to their infiltrative nature and heterogeneity. Our previous research revealed that glioma tumors in both animals and humans accumulate beta-amyloid protein (Aβ), detectable through immunohistochemical methods or staining with amyloid-specific dyes. We hypothesize that beta-amyloid-specific dyes could serve as glioma markers, potentially enabling the delineation of glioma tumors or targeted therapeutics delivery. In this study, the specificity and blood-brain barrier permeability of two fluorescent beta-amyloid-specific dyes, Brilliant Blue G (BBG) and BODIPY-based Amyloid Probe-1 (BAP-1), were evaluated in C57Bl/6 mouse glioma implantation models using GL261 and KR158 glioma cells. The findings demonstrate that both BBG and BAP-1 selectively stain gliomas, providing a clear contrast from normal brain tissue. The study results open avenues for further development of glioma visualization methods and targeted therapeutic delivery strategies for clinical applications.

## Linked entities

- **Proteins:** ab (abrupt)
- **Chemicals:** Brilliant Blue G (PubChem CID 61363)

## Full-text entities

- **Genes:** App (amyloid beta precursor protein) [NCBI Gene 11820] {aka Abeta, Abpp, Adap, Ag, Cvap, E030013M08Rik}
- **Diseases:** brain tumors (MESH:D001932), Gliomas (MESH:D005910)
- **Chemicals:** Amyloid Probe-1 (-), BBG (MESH:C004692), BODIPY (MESH:C095489)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** GL261 — Mus musculus (Mouse), Mouse glioblastoma, Cancer cell line (CVCL_Y003), C57Bl/6 — Mus musculus (Mouse), Mouse melanoma, Cancer cell line (CVCL_0192), KR158 — Xenopus laevis (African clawed frog), Spontaneously immortalized cell line (CVCL_VQ55)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12607655/full.md

## References

51 references — full list in the complete paper: https://tomesphere.com/paper/PMC12607655/full.md

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Source: https://tomesphere.com/paper/PMC12607655