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DCE-MRI-Derived Parameters in Evaluating Abraxane-Induced Early Vascular Response and the Effectiveness of Its Synergistic Interaction with Cisplatin

Our previous studies revealed molecular alterations of tumor vessels, varying from immature to mature alterations, resulting from Abraxane, and demonstrated that the integrin-specific PET tracer (18)F-FPPRGD2 can be used to noninvasively monitor such changes. However, changes in the tumor vasculatur...

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Autores principales: Sun, Xilin, Yang, Lili, Yan, Xuefeng, Sun, Yingying, Zhao, Dongliang, Ji, Yang, Wang, Kai, Chen, Xiaoyuan, Shen, Baozhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025193/
https://www.ncbi.nlm.nih.gov/pubmed/27632532
http://dx.doi.org/10.1371/journal.pone.0162601
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author Sun, Xilin
Yang, Lili
Yan, Xuefeng
Sun, Yingying
Zhao, Dongliang
Ji, Yang
Wang, Kai
Chen, Xiaoyuan
Shen, Baozhong
author_facet Sun, Xilin
Yang, Lili
Yan, Xuefeng
Sun, Yingying
Zhao, Dongliang
Ji, Yang
Wang, Kai
Chen, Xiaoyuan
Shen, Baozhong
author_sort Sun, Xilin
collection PubMed
description Our previous studies revealed molecular alterations of tumor vessels, varying from immature to mature alterations, resulting from Abraxane, and demonstrated that the integrin-specific PET tracer (18)F-FPPRGD2 can be used to noninvasively monitor such changes. However, changes in the tumor vasculature at functional levels such as perfusion and permeability are also important for monitoring Abraxane treatment outcomes in patients with cancer. The purpose of this study is to further investigate the vascular response during Abraxane therapy and the effectiveness of its synergistic interaction with cisplatin using Dynamic contrast enhanced-magnetic resonance imaging (DCE-MRI). Thirty MDA-MB-435 tumor mice were randomized into three groups: PBS control (C group), Abraxane only (A group), and sequential treatment with Abraxane followed by cisplatin (A-P group). Tumor volume was monitored based on caliper measurements. A DCE-MRI protocol was performed at baseline and day 3. The K(trans), K(ep) and V(e) were calculated and compared with CD31, α-SMA, and Ki67 histology data. Sequential treatment with Abraxane followed by cisplatin produced a significantly greater inhibition of tumor growth during the three weeks of the observation period. Decreases in K(trans) and K(ep) for the A and A-P groups were observed on day 3. Immunohistological staining suggested vascular remodeling during the Abraxane therapy. The changes in K(trans) and K(ep) values were correlated with alterations in the permeability of the tumor vasculature induced by the Abraxane treatment. In conclusion, Abraxane-mediated permeability variations in tumor vasculature can be quantitatively visualized by DCE-MRI, making this a useful method for studying the effects of early cancer treatment, especially the early vascular response. Vascular remodeling by Abraxane improves the efficiency of cisplatin delivery and thus results in a favorable treatment outcome.
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spelling pubmed-50251932016-09-27 DCE-MRI-Derived Parameters in Evaluating Abraxane-Induced Early Vascular Response and the Effectiveness of Its Synergistic Interaction with Cisplatin Sun, Xilin Yang, Lili Yan, Xuefeng Sun, Yingying Zhao, Dongliang Ji, Yang Wang, Kai Chen, Xiaoyuan Shen, Baozhong PLoS One Research Article Our previous studies revealed molecular alterations of tumor vessels, varying from immature to mature alterations, resulting from Abraxane, and demonstrated that the integrin-specific PET tracer (18)F-FPPRGD2 can be used to noninvasively monitor such changes. However, changes in the tumor vasculature at functional levels such as perfusion and permeability are also important for monitoring Abraxane treatment outcomes in patients with cancer. The purpose of this study is to further investigate the vascular response during Abraxane therapy and the effectiveness of its synergistic interaction with cisplatin using Dynamic contrast enhanced-magnetic resonance imaging (DCE-MRI). Thirty MDA-MB-435 tumor mice were randomized into three groups: PBS control (C group), Abraxane only (A group), and sequential treatment with Abraxane followed by cisplatin (A-P group). Tumor volume was monitored based on caliper measurements. A DCE-MRI protocol was performed at baseline and day 3. The K(trans), K(ep) and V(e) were calculated and compared with CD31, α-SMA, and Ki67 histology data. Sequential treatment with Abraxane followed by cisplatin produced a significantly greater inhibition of tumor growth during the three weeks of the observation period. Decreases in K(trans) and K(ep) for the A and A-P groups were observed on day 3. Immunohistological staining suggested vascular remodeling during the Abraxane therapy. The changes in K(trans) and K(ep) values were correlated with alterations in the permeability of the tumor vasculature induced by the Abraxane treatment. In conclusion, Abraxane-mediated permeability variations in tumor vasculature can be quantitatively visualized by DCE-MRI, making this a useful method for studying the effects of early cancer treatment, especially the early vascular response. Vascular remodeling by Abraxane improves the efficiency of cisplatin delivery and thus results in a favorable treatment outcome. Public Library of Science 2016-09-15 /pmc/articles/PMC5025193/ /pubmed/27632532 http://dx.doi.org/10.1371/journal.pone.0162601 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Sun, Xilin
Yang, Lili
Yan, Xuefeng
Sun, Yingying
Zhao, Dongliang
Ji, Yang
Wang, Kai
Chen, Xiaoyuan
Shen, Baozhong
DCE-MRI-Derived Parameters in Evaluating Abraxane-Induced Early Vascular Response and the Effectiveness of Its Synergistic Interaction with Cisplatin
title DCE-MRI-Derived Parameters in Evaluating Abraxane-Induced Early Vascular Response and the Effectiveness of Its Synergistic Interaction with Cisplatin
title_full DCE-MRI-Derived Parameters in Evaluating Abraxane-Induced Early Vascular Response and the Effectiveness of Its Synergistic Interaction with Cisplatin
title_fullStr DCE-MRI-Derived Parameters in Evaluating Abraxane-Induced Early Vascular Response and the Effectiveness of Its Synergistic Interaction with Cisplatin
title_full_unstemmed DCE-MRI-Derived Parameters in Evaluating Abraxane-Induced Early Vascular Response and the Effectiveness of Its Synergistic Interaction with Cisplatin
title_short DCE-MRI-Derived Parameters in Evaluating Abraxane-Induced Early Vascular Response and the Effectiveness of Its Synergistic Interaction with Cisplatin
title_sort dce-mri-derived parameters in evaluating abraxane-induced early vascular response and the effectiveness of its synergistic interaction with cisplatin
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025193/
https://www.ncbi.nlm.nih.gov/pubmed/27632532
http://dx.doi.org/10.1371/journal.pone.0162601
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