Molecular imaging of VEGF in gastrointestinal cancer in vivo using confocal laser endomicroscopy

Sebastian Foersch1, Ralf Kiesslich, Maximillian J Waldner

  • 1Medical Clinic I, University of Mainz, Mainz, Germany.

Gut
|July 20, 2010
PubMed
Abstract

Insights

Confocal laser endomicroscopy (CLE) allows in vivo molecular imaging of vascular endothelial growth factor (VEGF) in gastrointestinal cancers. This technique enables patient stratification and potential prediction of treatment response during colonoscopy.

Area of Science:

  • Gastroenterology
  • Oncology
  • Medical Imaging

Background:

  • Vascular endothelial growth factor (VEGF) is a key therapeutic target in gastrointestinal cancer (GiC).
  • Current endoscopic techniques lack the ability for in vivo visualization of VEGF.
  • Confocal laser endomicroscopy (CLE) offers subcellular resolution for in vivo gastrointestinal imaging.

Purpose of the Study:

  • To evaluate the efficacy of CLE for in vivo molecular imaging of VEGF in GiC.
  • To assess the potential of CLE for patient stratification in colorectal cancer (CRC).

Main Methods:

  • Labeled antibodies targeting VEGF were applied to tumors in APCmin mice, xenograft models, and human CRC specimens.
  • Tumor sites were scanned using CLE to detect specific fluorescent signals.
  • CLE findings were correlated with histology, immunohistochemistry (IHC), and ex vivo fluorescence microscopy.

Main Results:

  • VEGF-specific signals were visualized in vivo in murine tumors (13/15 APCmin mice, 9/10 xenografts) and human tissues (12/13 malignant, 10/11 healthy mucosa).
  • CLE's subcellular resolution allowed visualization of cytoplasmic VEGF distribution.
  • CLE findings demonstrated strong correlation with ex vivo microscopy.

Conclusions:

  • In vivo molecular imaging of VEGF using CLE is feasible in preclinical models and human tissues.
  • CLE is technically transferable to human colonoscopy for molecular imaging.
  • CLE holds potential for patient stratification and predicting treatment response in CRC.

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