Fluorescent affibody peptide penetration in glioma margin is superior to full antibody.

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...

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Main Authors: Kristian Sexton, Kenneth Tichauer, Kimberley S Samkoe, Jason Gunn, P Jack Hoopes, Brian W Pogue
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3625207?pdf=render
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spelling doaj-1aefe75ed5da40d3b34feaea00b855852020-11-25T01:52:49ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0184e6039010.1371/journal.pone.0060390Fluorescent affibody peptide penetration in glioma margin is superior to full antibody.Kristian SextonKenneth TichauerKimberley S SamkoeJason GunnP Jack HoopesBrian W PogueFluorescence 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).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.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.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.http://europepmc.org/articles/PMC3625207?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Kristian Sexton
Kenneth Tichauer
Kimberley S Samkoe
Jason Gunn
P Jack Hoopes
Brian W Pogue
spellingShingle Kristian Sexton
Kenneth Tichauer
Kimberley S Samkoe
Jason Gunn
P Jack Hoopes
Brian W Pogue
Fluorescent affibody peptide penetration in glioma margin is superior to full antibody.
PLoS ONE
author_facet Kristian Sexton
Kenneth Tichauer
Kimberley S Samkoe
Jason Gunn
P Jack Hoopes
Brian W Pogue
author_sort Kristian Sexton
title 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_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_sort fluorescent affibody peptide penetration in glioma margin is superior to full antibody.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description 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).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.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.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.
url http://europepmc.org/articles/PMC3625207?pdf=render
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