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Correlation of quantitative dynamic contrast‐enhanced MRI with microvascular density in necrotic, partial necrotic, and viable liver tumors in a rabbit model
The purpose of this study was to examine the correlation of quantitative dynamic contrast‐enhanced (DCE) magnetic resonance imaging (MRI) with microvessel density (MVD) in necrotic, partial necrotic, and viable tumors using a rabbit VX2 liver tumor model. Nine rabbits were used for this study. The c...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5874097/ https://www.ncbi.nlm.nih.gov/pubmed/27685133 http://dx.doi.org/10.1120/jacmp.v17i5.6314 |
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author | Moon, Jungwon Kim, Jae‐Hun Choi, Dongil Yang, Jehoon Lee, Min Woo Choi, Yoon‐La Rhim, MD, Hyunchul |
author_facet | Moon, Jungwon Kim, Jae‐Hun Choi, Dongil Yang, Jehoon Lee, Min Woo Choi, Yoon‐La Rhim, MD, Hyunchul |
author_sort | Moon, Jungwon |
collection | PubMed |
description | The purpose of this study was to examine the correlation of quantitative dynamic contrast‐enhanced (DCE) magnetic resonance imaging (MRI) with microvessel density (MVD) in necrotic, partial necrotic, and viable tumors using a rabbit VX2 liver tumor model. Nine rabbits were used for this study. The complete necrotic area (CNA), partial necrotic area (PNA), and viable tumor area (VTA) of liver tumors were experimentally induced by radiofrequency ablation (RFA). DCE‐MRI data were processed based on the extended Kety model to estimate [Formula: see text] and v(p) parameters. The boundaries among CNA, PNA, and VTA were delineated based on H&E stain images, and MVD was assessed for each subregion of each VX2 tumor based. There were no correlations between ph‐parameters ([Formula: see text] , and [Formula: see text]) and MVD for CNA. For PNA, the [Formula: see text] values were positively correlated with the MVD ([Formula: see text]). For VTA, we found a positive correlation between [Formula: see text] values and the MVD ([Formula: see text]). Measuring from both the PNA and the VTA, mean [Formula: see text] values were positively correlated with mean MVD ([Formula: see text]). In a rabbit VX2 liver tumor model, [Formula: see text] values correlated well with MVD counts of PNA and VTA in liver tumors. PACS number(s): 87.19.If MRI |
format | Online Article Text |
id | pubmed-5874097 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58740972018-04-02 Correlation of quantitative dynamic contrast‐enhanced MRI with microvascular density in necrotic, partial necrotic, and viable liver tumors in a rabbit model Moon, Jungwon Kim, Jae‐Hun Choi, Dongil Yang, Jehoon Lee, Min Woo Choi, Yoon‐La Rhim, MD, Hyunchul J Appl Clin Med Phys Medical Imaging The purpose of this study was to examine the correlation of quantitative dynamic contrast‐enhanced (DCE) magnetic resonance imaging (MRI) with microvessel density (MVD) in necrotic, partial necrotic, and viable tumors using a rabbit VX2 liver tumor model. Nine rabbits were used for this study. The complete necrotic area (CNA), partial necrotic area (PNA), and viable tumor area (VTA) of liver tumors were experimentally induced by radiofrequency ablation (RFA). DCE‐MRI data were processed based on the extended Kety model to estimate [Formula: see text] and v(p) parameters. The boundaries among CNA, PNA, and VTA were delineated based on H&E stain images, and MVD was assessed for each subregion of each VX2 tumor based. There were no correlations between ph‐parameters ([Formula: see text] , and [Formula: see text]) and MVD for CNA. For PNA, the [Formula: see text] values were positively correlated with the MVD ([Formula: see text]). For VTA, we found a positive correlation between [Formula: see text] values and the MVD ([Formula: see text]). Measuring from both the PNA and the VTA, mean [Formula: see text] values were positively correlated with mean MVD ([Formula: see text]). In a rabbit VX2 liver tumor model, [Formula: see text] values correlated well with MVD counts of PNA and VTA in liver tumors. PACS number(s): 87.19.If MRI John Wiley and Sons Inc. 2016-09-08 /pmc/articles/PMC5874097/ /pubmed/27685133 http://dx.doi.org/10.1120/jacmp.v17i5.6314 Text en © 2016 The Authors. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/3.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Medical Imaging Moon, Jungwon Kim, Jae‐Hun Choi, Dongil Yang, Jehoon Lee, Min Woo Choi, Yoon‐La Rhim, MD, Hyunchul Correlation of quantitative dynamic contrast‐enhanced MRI with microvascular density in necrotic, partial necrotic, and viable liver tumors in a rabbit model |
title | Correlation of quantitative dynamic contrast‐enhanced MRI with microvascular density in necrotic, partial necrotic, and viable liver tumors in a rabbit model |
title_full | Correlation of quantitative dynamic contrast‐enhanced MRI with microvascular density in necrotic, partial necrotic, and viable liver tumors in a rabbit model |
title_fullStr | Correlation of quantitative dynamic contrast‐enhanced MRI with microvascular density in necrotic, partial necrotic, and viable liver tumors in a rabbit model |
title_full_unstemmed | Correlation of quantitative dynamic contrast‐enhanced MRI with microvascular density in necrotic, partial necrotic, and viable liver tumors in a rabbit model |
title_short | Correlation of quantitative dynamic contrast‐enhanced MRI with microvascular density in necrotic, partial necrotic, and viable liver tumors in a rabbit model |
title_sort | correlation of quantitative dynamic contrast‐enhanced mri with microvascular density in necrotic, partial necrotic, and viable liver tumors in a rabbit model |
topic | Medical Imaging |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5874097/ https://www.ncbi.nlm.nih.gov/pubmed/27685133 http://dx.doi.org/10.1120/jacmp.v17i5.6314 |
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