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Fluorescent Affibody Peptide Penetration in Glioma Margin Is Superior to Full Antibody

OBJECT: Fluorescence imaging has the potential to significantly improve neurosurgical resection of oncologic lesions through improved differentiation between normal and cancerous tissue at the tumor margins. In order to successfully mark glioma tissue a fluorescent tracer must have the ability to pe...

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Autores principales: Sexton, Kristian, Tichauer, Kenneth, Samkoe, Kimberley S., Gunn, Jason, Hoopes, P. Jack, Pogue, Brian W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3625207/
https://www.ncbi.nlm.nih.gov/pubmed/23593208
http://dx.doi.org/10.1371/journal.pone.0060390
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author Sexton, Kristian
Tichauer, Kenneth
Samkoe, Kimberley S.
Gunn, Jason
Hoopes, P. Jack
Pogue, Brian W.
author_facet Sexton, Kristian
Tichauer, Kenneth
Samkoe, Kimberley S.
Gunn, Jason
Hoopes, P. Jack
Pogue, Brian W.
author_sort Sexton, Kristian
collection PubMed
description OBJECT: Fluorescence imaging has the potential to significantly improve neurosurgical resection of oncologic lesions through improved differentiation between normal and cancerous tissue at the tumor margins. In order to successfully mark glioma tissue a fluorescent tracer must have the ability to penetrate through the blood brain barrier (BBB) and provide delineation in the tumor periphery where heterogeneously intact BBB may exist. In this study it was hypothesized that, due to its smaller size, fluorescently labeled anti-EGFR Affibody protein (∼7 kDa) would provide a more clear delineation of the tumor margin than would fluorescently labeled cetuximab, a full antibody (∼150 kDa) to the epidermal growth factor receptor (EGFR). METHODS: Cetuximab and anti-EGFR targeted Affibody were conjugated to two different fluorescent dyes (both emitting in the near-infrared) and injected intravenously into 6 athymic mice which were inoculated orthotopically with green fluorescent protein (GFP) expressing human U251 glioma cells. Each mouse was sacrificed at 1-h post injection, at which time brains were removed, snap frozen, sectioned and quantitatively analyzed for fluorescence distribution. RESULTS: Ex vivo analysis showed on average, nearly equal concentrations of cetuximab and Affibody within the tumor (on average Affibody made up 49±6% of injected protein), however, the cetuximab was more confined to the center of the tumor with Affibody showing significantly higher concentrations at the tumor periphery (on average Affibody made up 72±15% of injected protein in the outer 50 um of the tumor). Further ex vivo analysis of detection studies showed that the Affibody provided superior discrimination for differentiation of tumor from surrounding normal brain. CONCLUSIONS: The present study indicates that fluorescently labeled anti-EGFR Affibody can provide significantly better delineation of tumor margins than a fluorescently labeled anti-EGFR antibody and shows considerable potential for guiding margin detection during neurosurgery.
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spelling pubmed-36252072013-04-16 Fluorescent Affibody Peptide Penetration in Glioma Margin Is Superior to Full Antibody Sexton, Kristian Tichauer, Kenneth Samkoe, Kimberley S. Gunn, Jason Hoopes, P. Jack Pogue, Brian W. PLoS One Research Article OBJECT: Fluorescence imaging has the potential to significantly improve neurosurgical resection of oncologic lesions through improved differentiation between normal and cancerous tissue at the tumor margins. In order to successfully mark glioma tissue a fluorescent tracer must have the ability to penetrate through the blood brain barrier (BBB) and provide delineation in the tumor periphery where heterogeneously intact BBB may exist. In this study it was hypothesized that, due to its smaller size, fluorescently labeled anti-EGFR Affibody protein (∼7 kDa) would provide a more clear delineation of the tumor margin than would fluorescently labeled cetuximab, a full antibody (∼150 kDa) to the epidermal growth factor receptor (EGFR). METHODS: Cetuximab and anti-EGFR targeted Affibody were conjugated to two different fluorescent dyes (both emitting in the near-infrared) and injected intravenously into 6 athymic mice which were inoculated orthotopically with green fluorescent protein (GFP) expressing human U251 glioma cells. Each mouse was sacrificed at 1-h post injection, at which time brains were removed, snap frozen, sectioned and quantitatively analyzed for fluorescence distribution. RESULTS: Ex vivo analysis showed on average, nearly equal concentrations of cetuximab and Affibody within the tumor (on average Affibody made up 49±6% of injected protein), however, the cetuximab was more confined to the center of the tumor with Affibody showing significantly higher concentrations at the tumor periphery (on average Affibody made up 72±15% of injected protein in the outer 50 um of the tumor). Further ex vivo analysis of detection studies showed that the Affibody provided superior discrimination for differentiation of tumor from surrounding normal brain. CONCLUSIONS: The present study indicates that fluorescently labeled anti-EGFR Affibody can provide significantly better delineation of tumor margins than a fluorescently labeled anti-EGFR antibody and shows considerable potential for guiding margin detection during neurosurgery. Public Library of Science 2013-04-12 /pmc/articles/PMC3625207/ /pubmed/23593208 http://dx.doi.org/10.1371/journal.pone.0060390 Text en © 2013 Sexton et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Sexton, Kristian
Tichauer, Kenneth
Samkoe, Kimberley S.
Gunn, Jason
Hoopes, P. Jack
Pogue, Brian W.
Fluorescent Affibody Peptide Penetration in Glioma Margin Is Superior to Full Antibody
title Fluorescent Affibody Peptide Penetration in Glioma Margin Is Superior to Full Antibody
title_full Fluorescent Affibody Peptide Penetration in Glioma Margin Is Superior to Full Antibody
title_fullStr Fluorescent Affibody Peptide Penetration in Glioma Margin Is Superior to Full Antibody
title_full_unstemmed Fluorescent Affibody Peptide Penetration in Glioma Margin Is Superior to Full Antibody
title_short Fluorescent Affibody Peptide Penetration in Glioma Margin Is Superior to Full Antibody
title_sort fluorescent affibody peptide penetration in glioma margin is superior to full antibody
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3625207/
https://www.ncbi.nlm.nih.gov/pubmed/23593208
http://dx.doi.org/10.1371/journal.pone.0060390
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