# A Glucosylated BODIPY Uses the GLUT Channel to Target Cancer Cells in In Vitro and In Vivo Models

**Authors:** Marta Turati, Giacomo Biagiotti, Cosetta Ravelli, Chiara Tobia, Jacopo Cardellini, Luca Mignani, Jacopo Tricomi, Debora Berti, Stefano Cicchi, Barbara Richichi, Roberto Ronca

PMC · DOI: 10.1021/acsomega.5c06410 · 2025-11-07

## TL;DR

This study introduces a glucosylated BODIPY that targets cancer cells using glucose transporters, showing potential for cancer imaging and treatment.

## Contribution

A novel glucosylated BODIPY probe is developed for broad-spectrum cancer targeting via GLUT channels.

## Key findings

- Glc-BODIPY effectively targets various cancer cell types in vitro.
- The probe demonstrates tumor-targeting ability in in vivo models.
- The use of d-glucose enhances targeting by exploiting cancer cell metabolism.

## Abstract

The conjugation of
fluorescent probes to tumor-targeting molecules
represents a promising strategy for the development of precision cancer
bioimaging and treatment. Among the different tumor-targeting strategies,
the use of d-glucose residues, which exploit the high energy
demand of cancer cells, can enable recognition by a broad spectrum
of tumors, thus overcoming limitations related to cancer heterogeneity.
In this study, we combined the distinctive optical properties of BODIPY-based
probes with the known tumor-targeting abilities of d-glucose.
We report on the characterization of a glucosylated BODIPY, named Glc-BODIPY, and its ability to target different cancer cell
types in both in vitro and in vivo models.

## Linked entities

- **Chemicals:** BODIPY (PubChem CID 25058173), d-glucose (PubChem CID 5793)
- **Diseases:** cancer (MONDO:0004992)

## Full-text entities

- **Genes:** SLC2A1 (solute carrier family 2 member 1) [NCBI Gene 6513] {aka CSE, DYT17, DYT18, DYT9, EIG12, GLUT}
- **Diseases:** Cancer (MESH:D009369)
- **Chemicals:** BODIPY (MESH:C095489), Glc-BODIPY (-), d-glucose (MESH:D005947)

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12631688/full.md

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Source: https://tomesphere.com/paper/PMC12631688