Specific visualization of glioma cells in living low-grade tumor tissue.

<h4>Background</h4>The current therapy of malignant gliomas is based on surgical resection, radio-chemotherapy and chemotherapy. Recent retrospective case-series have highlighted the significance of the extent of resection as a prognostic factor predicting the course of the disease. Comp...

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Main Authors: Sven R Kantelhardt, Wouter Caarls, Anthony H B de Vries, Guy M Hagen, Thomas M Jovin, Walter Schulz-Schaeffer, Veit Rohde, Alf Giese, Donna J Arndt-Jovin
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-06-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20614029/?tool=EBI
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author Sven R Kantelhardt
Wouter Caarls
Anthony H B de Vries
Guy M Hagen
Thomas M Jovin
Walter Schulz-Schaeffer
Veit Rohde
Alf Giese
Donna J Arndt-Jovin
author_facet Sven R Kantelhardt
Wouter Caarls
Anthony H B de Vries
Guy M Hagen
Thomas M Jovin
Walter Schulz-Schaeffer
Veit Rohde
Alf Giese
Donna J Arndt-Jovin
author_sort Sven R Kantelhardt
collection DOAJ
description <h4>Background</h4>The current therapy of malignant gliomas is based on surgical resection, radio-chemotherapy and chemotherapy. Recent retrospective case-series have highlighted the significance of the extent of resection as a prognostic factor predicting the course of the disease. Complete resection in low-grade gliomas that show no MRI-enhanced images are especially difficult. The aim in this study was to develop a robust, specific, new fluorescent probe for glioma cells that is easy to apply to live tumor biopsies and could identify tumor cells from normal brain cells at all levels of magnification.<h4>Methodology/principal findings</h4>In this investigation we employed brightly fluorescent, photostable quantum dots (QDs) to specifically target epidermal growth factor receptor (EGFR) that is upregulated in many gliomas. Living glioma and normal cells or tissue biopsies were incubated with QDs coupled to EGF and/or monoclonal antibodies against EGFR for 30 minutes, washed and imaged. The data include results from cell-culture, animal model and ex vivo human tumor biopsies of both low-grade and high-grade gliomas and show high probe specificity. Tumor cells could be visualized from the macroscopic to single cell level with contrast ratios as high as 1000: 1 compared to normal brain tissue.<h4>Conclusions/significance</h4>The ability of the targeted probes to clearly distinguish tumor cells in low-grade tumor biopsies, where no enhanced MRI image was obtained, demonstrates the great potential of the method. We propose that future application of specifically targeted fluorescent particles during surgery could allow intraoperative guidance for the removal of residual tumor cells from the resection cavity and thus increase patient survival.
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spelling doaj.art-9c184c9dde40499fa32bef8084b017952022-12-21T21:46:42ZengPublic Library of Science (PLoS)PLoS ONE1932-62032010-06-0156e1132310.1371/journal.pone.0011323Specific visualization of glioma cells in living low-grade tumor tissue.Sven R KantelhardtWouter CaarlsAnthony H B de VriesGuy M HagenThomas M JovinWalter Schulz-SchaefferVeit RohdeAlf GieseDonna J Arndt-Jovin<h4>Background</h4>The current therapy of malignant gliomas is based on surgical resection, radio-chemotherapy and chemotherapy. Recent retrospective case-series have highlighted the significance of the extent of resection as a prognostic factor predicting the course of the disease. Complete resection in low-grade gliomas that show no MRI-enhanced images are especially difficult. The aim in this study was to develop a robust, specific, new fluorescent probe for glioma cells that is easy to apply to live tumor biopsies and could identify tumor cells from normal brain cells at all levels of magnification.<h4>Methodology/principal findings</h4>In this investigation we employed brightly fluorescent, photostable quantum dots (QDs) to specifically target epidermal growth factor receptor (EGFR) that is upregulated in many gliomas. Living glioma and normal cells or tissue biopsies were incubated with QDs coupled to EGF and/or monoclonal antibodies against EGFR for 30 minutes, washed and imaged. The data include results from cell-culture, animal model and ex vivo human tumor biopsies of both low-grade and high-grade gliomas and show high probe specificity. Tumor cells could be visualized from the macroscopic to single cell level with contrast ratios as high as 1000: 1 compared to normal brain tissue.<h4>Conclusions/significance</h4>The ability of the targeted probes to clearly distinguish tumor cells in low-grade tumor biopsies, where no enhanced MRI image was obtained, demonstrates the great potential of the method. We propose that future application of specifically targeted fluorescent particles during surgery could allow intraoperative guidance for the removal of residual tumor cells from the resection cavity and thus increase patient survival.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20614029/?tool=EBI
spellingShingle Sven R Kantelhardt
Wouter Caarls
Anthony H B de Vries
Guy M Hagen
Thomas M Jovin
Walter Schulz-Schaeffer
Veit Rohde
Alf Giese
Donna J Arndt-Jovin
Specific visualization of glioma cells in living low-grade tumor tissue.
PLoS ONE
title Specific visualization of glioma cells in living low-grade tumor tissue.
title_full Specific visualization of glioma cells in living low-grade tumor tissue.
title_fullStr Specific visualization of glioma cells in living low-grade tumor tissue.
title_full_unstemmed Specific visualization of glioma cells in living low-grade tumor tissue.
title_short Specific visualization of glioma cells in living low-grade tumor tissue.
title_sort specific visualization of glioma cells in living low grade tumor tissue
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20614029/?tool=EBI
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