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Imaging heterogeneity of peptide delivery and binding in solid tumors using SPECT imaging and MRI

BACKGROUND: As model system, a solid-tumor patient-derived xenograft (PDX) model characterized by high peptide receptor expression and histological tissue homogeneity was used to study radiopeptide targeting. In this solid-tumor model, high tumor uptake of targeting peptides was expected. However, i...

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Autores principales: Haeck, J. C., Bol, K., de Ridder, C. M. A., Brunel, L., Fehrentz, J. A., Martinez, J., van Weerden, W. M., Bernsen, M. R., de Jong, M., Veenland, J. F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4713394/
https://www.ncbi.nlm.nih.gov/pubmed/26769345
http://dx.doi.org/10.1186/s13550-016-0160-4
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author Haeck, J. C.
Bol, K.
de Ridder, C. M. A.
Brunel, L.
Fehrentz, J. A.
Martinez, J.
van Weerden, W. M.
Bernsen, M. R.
de Jong, M.
Veenland, J. F.
author_facet Haeck, J. C.
Bol, K.
de Ridder, C. M. A.
Brunel, L.
Fehrentz, J. A.
Martinez, J.
van Weerden, W. M.
Bernsen, M. R.
de Jong, M.
Veenland, J. F.
author_sort Haeck, J. C.
collection PubMed
description BACKGROUND: As model system, a solid-tumor patient-derived xenograft (PDX) model characterized by high peptide receptor expression and histological tissue homogeneity was used to study radiopeptide targeting. In this solid-tumor model, high tumor uptake of targeting peptides was expected. However, in vivo SPECT images showed substantial heterogeneous radioactivity accumulation despite homogenous receptor distribution in the tumor xenografts as assessed by in vitro autoradiography. We hypothesized that delivery of peptide to the tumor cells is dictated by adequate local tumor perfusion. To study this relationship, sequential SPECT/CT and MRI were performed to assess the role of vascular functionality in radiopeptide accumulation. METHODS: High-resolution SPECT and dynamic contrast-enhanced (DCE)-MRI were acquired in six mice bearing PC295 PDX tumors expressing the gastrin-releasing peptide (GRP) receptor. Two hours prior to SPECT imaging, animals received 25 MBq (111)In(DOTA-(βAla)2-JMV594) (25 pmol). Images were acquired using multipinhole SPECT/CT. Directly after SPECT imaging, MR images were acquired on a 7.0-T dedicated animal scanner. DCE-MR images were quantified using semi-quantitative and quantitative models. The DCE-MR and SPECT images were spatially aligned to compute the correlations between radioactivity and DCE-MRI-derived parameters over the tumor. RESULTS: Whereas histology, in vitro autoradiography, and multiple-weighted MRI scans all showed homogenous tissue characteristics, both SPECT and DCE-MRI showed heterogeneous distribution patterns throughout the tumor. The average Spearman’s correlation coefficient between SPECT and DCE-MRI ranged from 0.57 to 0.63 for the “exchange-related” DCE-MRI perfusion parameters. CONCLUSIONS: A positive correlation was shown between exchange-related DCE-MRI perfusion parameters and the amount of radioactivity accumulated as measured by SPECT, demonstrating that vascular function was an important aspect of radiopeptide distribution in solid tumors. The combined use of SPECT and MRI added crucial information on the perfusion efficiency versus radiopeptide uptake in solid tumors and showed that functional tumor characteristics varied locally even when the tissue appeared homogenous on current standard assessment techniques. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13550-016-0160-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-47133942016-01-31 Imaging heterogeneity of peptide delivery and binding in solid tumors using SPECT imaging and MRI Haeck, J. C. Bol, K. de Ridder, C. M. A. Brunel, L. Fehrentz, J. A. Martinez, J. van Weerden, W. M. Bernsen, M. R. de Jong, M. Veenland, J. F. EJNMMI Res Original Research BACKGROUND: As model system, a solid-tumor patient-derived xenograft (PDX) model characterized by high peptide receptor expression and histological tissue homogeneity was used to study radiopeptide targeting. In this solid-tumor model, high tumor uptake of targeting peptides was expected. However, in vivo SPECT images showed substantial heterogeneous radioactivity accumulation despite homogenous receptor distribution in the tumor xenografts as assessed by in vitro autoradiography. We hypothesized that delivery of peptide to the tumor cells is dictated by adequate local tumor perfusion. To study this relationship, sequential SPECT/CT and MRI were performed to assess the role of vascular functionality in radiopeptide accumulation. METHODS: High-resolution SPECT and dynamic contrast-enhanced (DCE)-MRI were acquired in six mice bearing PC295 PDX tumors expressing the gastrin-releasing peptide (GRP) receptor. Two hours prior to SPECT imaging, animals received 25 MBq (111)In(DOTA-(βAla)2-JMV594) (25 pmol). Images were acquired using multipinhole SPECT/CT. Directly after SPECT imaging, MR images were acquired on a 7.0-T dedicated animal scanner. DCE-MR images were quantified using semi-quantitative and quantitative models. The DCE-MR and SPECT images were spatially aligned to compute the correlations between radioactivity and DCE-MRI-derived parameters over the tumor. RESULTS: Whereas histology, in vitro autoradiography, and multiple-weighted MRI scans all showed homogenous tissue characteristics, both SPECT and DCE-MRI showed heterogeneous distribution patterns throughout the tumor. The average Spearman’s correlation coefficient between SPECT and DCE-MRI ranged from 0.57 to 0.63 for the “exchange-related” DCE-MRI perfusion parameters. CONCLUSIONS: A positive correlation was shown between exchange-related DCE-MRI perfusion parameters and the amount of radioactivity accumulated as measured by SPECT, demonstrating that vascular function was an important aspect of radiopeptide distribution in solid tumors. The combined use of SPECT and MRI added crucial information on the perfusion efficiency versus radiopeptide uptake in solid tumors and showed that functional tumor characteristics varied locally even when the tissue appeared homogenous on current standard assessment techniques. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13550-016-0160-4) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2016-01-14 /pmc/articles/PMC4713394/ /pubmed/26769345 http://dx.doi.org/10.1186/s13550-016-0160-4 Text en © Haeck et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Research
Haeck, J. C.
Bol, K.
de Ridder, C. M. A.
Brunel, L.
Fehrentz, J. A.
Martinez, J.
van Weerden, W. M.
Bernsen, M. R.
de Jong, M.
Veenland, J. F.
Imaging heterogeneity of peptide delivery and binding in solid tumors using SPECT imaging and MRI
title Imaging heterogeneity of peptide delivery and binding in solid tumors using SPECT imaging and MRI
title_full Imaging heterogeneity of peptide delivery and binding in solid tumors using SPECT imaging and MRI
title_fullStr Imaging heterogeneity of peptide delivery and binding in solid tumors using SPECT imaging and MRI
title_full_unstemmed Imaging heterogeneity of peptide delivery and binding in solid tumors using SPECT imaging and MRI
title_short Imaging heterogeneity of peptide delivery and binding in solid tumors using SPECT imaging and MRI
title_sort imaging heterogeneity of peptide delivery and binding in solid tumors using spect imaging and mri
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4713394/
https://www.ncbi.nlm.nih.gov/pubmed/26769345
http://dx.doi.org/10.1186/s13550-016-0160-4
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