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In-Vivo Retention of 5-Fluorouracil Using (19)F Magnetic Resonance Chemical Shift Imaging in Colorectal Cancer in a Murine Model

Colorectal cancer is the third leading cause of cancer death worldwide. 5-Fluorouracil (5-FU) is one of the most commonly used chemotherapies for treatment of solid tumours, including colorectal cancer. The efficacy of treatment is dependent on tumour type and can only be determined six weeks after...

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Autores principales: Shepelytskyi, Yurii, Fox, Matthew S., Davenport, Karen, Li, Tao, Albert, Mitchell S., Davenport, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6744414/
https://www.ncbi.nlm.nih.gov/pubmed/31519979
http://dx.doi.org/10.1038/s41598-019-49716-7
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author Shepelytskyi, Yurii
Fox, Matthew S.
Davenport, Karen
Li, Tao
Albert, Mitchell S.
Davenport, Eric
author_facet Shepelytskyi, Yurii
Fox, Matthew S.
Davenport, Karen
Li, Tao
Albert, Mitchell S.
Davenport, Eric
author_sort Shepelytskyi, Yurii
collection PubMed
description Colorectal cancer is the third leading cause of cancer death worldwide. 5-Fluorouracil (5-FU) is one of the most commonly used chemotherapies for treatment of solid tumours, including colorectal cancer. The efficacy of treatment is dependent on tumour type and can only be determined six weeks after beginning chemotherapy, with only 40–50% of patients responding positively to the 5-FU therapy. In this paper, we demonstrate the potential of using Magnetic Resonance (MR) Chemical Shift Imaging (CSI) for in-vivo monitoring of 5-FU tumor-retention in two different colorectal tumour types (HT-29 & H-508). Time curves for 5-FU signals from the liver and bladder were also acquired. We observed significant differences (p < 0.01) in 5-FU signal time dependencies for the HT-29 and H-508 tumours. Retention of 5-FU occurred in the H-508 tumour, whereas the HT-29 tumour is not expected to retain 5FU due to the observation of the negative b time constant indicating a decline in 5FU within the tumour. This study successfully demonstrates that CSI may be a useful tool for early identification of 5-FU responsive tumours based on observed tumour retention of the 5-FU.
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spelling pubmed-67444142019-09-27 In-Vivo Retention of 5-Fluorouracil Using (19)F Magnetic Resonance Chemical Shift Imaging in Colorectal Cancer in a Murine Model Shepelytskyi, Yurii Fox, Matthew S. Davenport, Karen Li, Tao Albert, Mitchell S. Davenport, Eric Sci Rep Article Colorectal cancer is the third leading cause of cancer death worldwide. 5-Fluorouracil (5-FU) is one of the most commonly used chemotherapies for treatment of solid tumours, including colorectal cancer. The efficacy of treatment is dependent on tumour type and can only be determined six weeks after beginning chemotherapy, with only 40–50% of patients responding positively to the 5-FU therapy. In this paper, we demonstrate the potential of using Magnetic Resonance (MR) Chemical Shift Imaging (CSI) for in-vivo monitoring of 5-FU tumor-retention in two different colorectal tumour types (HT-29 & H-508). Time curves for 5-FU signals from the liver and bladder were also acquired. We observed significant differences (p < 0.01) in 5-FU signal time dependencies for the HT-29 and H-508 tumours. Retention of 5-FU occurred in the H-508 tumour, whereas the HT-29 tumour is not expected to retain 5FU due to the observation of the negative b time constant indicating a decline in 5FU within the tumour. This study successfully demonstrates that CSI may be a useful tool for early identification of 5-FU responsive tumours based on observed tumour retention of the 5-FU. Nature Publishing Group UK 2019-09-13 /pmc/articles/PMC6744414/ /pubmed/31519979 http://dx.doi.org/10.1038/s41598-019-49716-7 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Shepelytskyi, Yurii
Fox, Matthew S.
Davenport, Karen
Li, Tao
Albert, Mitchell S.
Davenport, Eric
In-Vivo Retention of 5-Fluorouracil Using (19)F Magnetic Resonance Chemical Shift Imaging in Colorectal Cancer in a Murine Model
title In-Vivo Retention of 5-Fluorouracil Using (19)F Magnetic Resonance Chemical Shift Imaging in Colorectal Cancer in a Murine Model
title_full In-Vivo Retention of 5-Fluorouracil Using (19)F Magnetic Resonance Chemical Shift Imaging in Colorectal Cancer in a Murine Model
title_fullStr In-Vivo Retention of 5-Fluorouracil Using (19)F Magnetic Resonance Chemical Shift Imaging in Colorectal Cancer in a Murine Model
title_full_unstemmed In-Vivo Retention of 5-Fluorouracil Using (19)F Magnetic Resonance Chemical Shift Imaging in Colorectal Cancer in a Murine Model
title_short In-Vivo Retention of 5-Fluorouracil Using (19)F Magnetic Resonance Chemical Shift Imaging in Colorectal Cancer in a Murine Model
title_sort in-vivo retention of 5-fluorouracil using (19)f magnetic resonance chemical shift imaging in colorectal cancer in a murine model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6744414/
https://www.ncbi.nlm.nih.gov/pubmed/31519979
http://dx.doi.org/10.1038/s41598-019-49716-7
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