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Evaluation of metronomic chemotherapy response using diffusion and dynamic contrast-enhanced MRI
PURPOSE: To investigate the feasibility of using diffusion MRI (dMRI) and dynamic contrast-enhanced (DCE) MRI to evaluate the treatment response of metronomic chemotherapy (MCT) in the 4T1 mammary tumor model of locally advanced breast cancer. METHODS: Twelve Balb/c mice with metastatic breast cance...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7688103/ https://www.ncbi.nlm.nih.gov/pubmed/33237905 http://dx.doi.org/10.1371/journal.pone.0241916 |
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author | Baboli, Mehran Winters, Kerryanne V. Freed, Melanie Zhang, Jin Kim, Sungheon Gene |
author_facet | Baboli, Mehran Winters, Kerryanne V. Freed, Melanie Zhang, Jin Kim, Sungheon Gene |
author_sort | Baboli, Mehran |
collection | PubMed |
description | PURPOSE: To investigate the feasibility of using diffusion MRI (dMRI) and dynamic contrast-enhanced (DCE) MRI to evaluate the treatment response of metronomic chemotherapy (MCT) in the 4T1 mammary tumor model of locally advanced breast cancer. METHODS: Twelve Balb/c mice with metastatic breast cancer were divided into treated and untreated (control) groups. The treated group (n = 6) received five treatments of anti-metabolite agent 5-Fluorouracil (5FU) in the span of two weeks. dMRI and DCE-MRI were acquired for both treated and control groups before and after MCT. Immunohistochemically staining and measurements were performed after the post-MRI measurements for comparison. RESULTS: The control mice had significantly (p<0.005) larger tumors than the MCT treated mice. The DCE-MRI analysis showed a decrease in contrast enhancement for the control group, whereas the MCT mice had a more stable enhancement between the pre-chemo and post-chemo time points. This confirms the antiangiogenic effects of 5FU treatment. Comparing amplitude of enhancement revealed a significantly (p<0.05) higher enhancement in the MCT tumors than in the controls. Moreover, the MCT uptake rate was significantly (p<0.001) slower than the controls. dMRI analysis showed the MCT ADC values were significantly larger than the control group at the post-scan time point. CONCLUSION: dMRI and DCE-MRI can be used as potential biomarkers for assessing the treatment response of MCT. The MRI and pathology observations suggested that in addition to the cytotoxic effect of cell kills, the MCT with a cytotoxic drug, 5FU, induced changes in the tumor vasculature similar to the anti-angiogenic effect. |
format | Online Article Text |
id | pubmed-7688103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-76881032020-12-05 Evaluation of metronomic chemotherapy response using diffusion and dynamic contrast-enhanced MRI Baboli, Mehran Winters, Kerryanne V. Freed, Melanie Zhang, Jin Kim, Sungheon Gene PLoS One Research Article PURPOSE: To investigate the feasibility of using diffusion MRI (dMRI) and dynamic contrast-enhanced (DCE) MRI to evaluate the treatment response of metronomic chemotherapy (MCT) in the 4T1 mammary tumor model of locally advanced breast cancer. METHODS: Twelve Balb/c mice with metastatic breast cancer were divided into treated and untreated (control) groups. The treated group (n = 6) received five treatments of anti-metabolite agent 5-Fluorouracil (5FU) in the span of two weeks. dMRI and DCE-MRI were acquired for both treated and control groups before and after MCT. Immunohistochemically staining and measurements were performed after the post-MRI measurements for comparison. RESULTS: The control mice had significantly (p<0.005) larger tumors than the MCT treated mice. The DCE-MRI analysis showed a decrease in contrast enhancement for the control group, whereas the MCT mice had a more stable enhancement between the pre-chemo and post-chemo time points. This confirms the antiangiogenic effects of 5FU treatment. Comparing amplitude of enhancement revealed a significantly (p<0.05) higher enhancement in the MCT tumors than in the controls. Moreover, the MCT uptake rate was significantly (p<0.001) slower than the controls. dMRI analysis showed the MCT ADC values were significantly larger than the control group at the post-scan time point. CONCLUSION: dMRI and DCE-MRI can be used as potential biomarkers for assessing the treatment response of MCT. The MRI and pathology observations suggested that in addition to the cytotoxic effect of cell kills, the MCT with a cytotoxic drug, 5FU, induced changes in the tumor vasculature similar to the anti-angiogenic effect. Public Library of Science 2020-11-25 /pmc/articles/PMC7688103/ /pubmed/33237905 http://dx.doi.org/10.1371/journal.pone.0241916 Text en © 2020 Baboli 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Baboli, Mehran Winters, Kerryanne V. Freed, Melanie Zhang, Jin Kim, Sungheon Gene Evaluation of metronomic chemotherapy response using diffusion and dynamic contrast-enhanced MRI |
title | Evaluation of metronomic chemotherapy response using diffusion and dynamic contrast-enhanced MRI |
title_full | Evaluation of metronomic chemotherapy response using diffusion and dynamic contrast-enhanced MRI |
title_fullStr | Evaluation of metronomic chemotherapy response using diffusion and dynamic contrast-enhanced MRI |
title_full_unstemmed | Evaluation of metronomic chemotherapy response using diffusion and dynamic contrast-enhanced MRI |
title_short | Evaluation of metronomic chemotherapy response using diffusion and dynamic contrast-enhanced MRI |
title_sort | evaluation of metronomic chemotherapy response using diffusion and dynamic contrast-enhanced mri |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7688103/ https://www.ncbi.nlm.nih.gov/pubmed/33237905 http://dx.doi.org/10.1371/journal.pone.0241916 |
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