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Treatment of false‐negative metastatic lymph nodes by a lymphatic drug delivery system with 5‐fluorouracil
Metastatic lymph nodes (LNs) may be the origin of systemic metastases. It will be important to develop a strategy that prevents systemic metastasis by treating these LNs at an early stage. False‐negative metastatic LNs, which are found during the early stage of metastasis development, are those that...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6536938/ https://www.ncbi.nlm.nih.gov/pubmed/30945479 http://dx.doi.org/10.1002/cam4.2125 |
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author | Fujii, Honoka Horie, Sachiko Sukhbaatar, Ariunbuyan Mishra, Radhika Sakamoto, Maya Mori, Shiro Kodama, Tetsuya |
author_facet | Fujii, Honoka Horie, Sachiko Sukhbaatar, Ariunbuyan Mishra, Radhika Sakamoto, Maya Mori, Shiro Kodama, Tetsuya |
author_sort | Fujii, Honoka |
collection | PubMed |
description | Metastatic lymph nodes (LNs) may be the origin of systemic metastases. It will be important to develop a strategy that prevents systemic metastasis by treating these LNs at an early stage. False‐negative metastatic LNs, which are found during the early stage of metastasis development, are those that contain tumor cells but have a size and shape similar to LNs that do not host tumor cells. Here, we show that 5‐fluorouracil (5‐FU), delivered by means of a novel lymphatic drug delivery system (LDDS), can treat LNs with false‐negative metastases in a mouse model. The effects of 5‐FU on four cell lines were investigated using in vitro cytotoxicity and cell survival assays. The therapeutic effects of LDDS‐administered 5‐FU on false‐negative metastatic LNs were evaluated using bioluminescence imaging, high‐frequency ultrasound (US), and histology in MHX10/Mo‐lpr/lpr mice. These experimental animals develop LNs that are similar in size to human LNs. We found that all cell lines showed sensitivity to 5‐FU in the in vitro assays. Furthermore, a concentration‐dependent effect of 5‐FU to inhibit tumor growth was observed in tumor cells with low invasive growth characteristics, although a significant reduction in metastatic LN volume was not detected in MHX10/Mo‐lpr/lpr mice. Adverse effects of 5‐FU were not detected. 5‐Fluorouracil administration with a LDDS is an effective treatment method for false‐negative metastatic LNs. We anticipate that the delivery of anticancer drugs by a LDDS will be of great benefit in the prevention and treatment of cancer metastasis via LNs. |
format | Online Article Text |
id | pubmed-6536938 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65369382019-06-03 Treatment of false‐negative metastatic lymph nodes by a lymphatic drug delivery system with 5‐fluorouracil Fujii, Honoka Horie, Sachiko Sukhbaatar, Ariunbuyan Mishra, Radhika Sakamoto, Maya Mori, Shiro Kodama, Tetsuya Cancer Med Clinical Cancer Research Metastatic lymph nodes (LNs) may be the origin of systemic metastases. It will be important to develop a strategy that prevents systemic metastasis by treating these LNs at an early stage. False‐negative metastatic LNs, which are found during the early stage of metastasis development, are those that contain tumor cells but have a size and shape similar to LNs that do not host tumor cells. Here, we show that 5‐fluorouracil (5‐FU), delivered by means of a novel lymphatic drug delivery system (LDDS), can treat LNs with false‐negative metastases in a mouse model. The effects of 5‐FU on four cell lines were investigated using in vitro cytotoxicity and cell survival assays. The therapeutic effects of LDDS‐administered 5‐FU on false‐negative metastatic LNs were evaluated using bioluminescence imaging, high‐frequency ultrasound (US), and histology in MHX10/Mo‐lpr/lpr mice. These experimental animals develop LNs that are similar in size to human LNs. We found that all cell lines showed sensitivity to 5‐FU in the in vitro assays. Furthermore, a concentration‐dependent effect of 5‐FU to inhibit tumor growth was observed in tumor cells with low invasive growth characteristics, although a significant reduction in metastatic LN volume was not detected in MHX10/Mo‐lpr/lpr mice. Adverse effects of 5‐FU were not detected. 5‐Fluorouracil administration with a LDDS is an effective treatment method for false‐negative metastatic LNs. We anticipate that the delivery of anticancer drugs by a LDDS will be of great benefit in the prevention and treatment of cancer metastasis via LNs. John Wiley and Sons Inc. 2019-04-03 /pmc/articles/PMC6536938/ /pubmed/30945479 http://dx.doi.org/10.1002/cam4.2125 Text en © 2019 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Cancer Research Fujii, Honoka Horie, Sachiko Sukhbaatar, Ariunbuyan Mishra, Radhika Sakamoto, Maya Mori, Shiro Kodama, Tetsuya Treatment of false‐negative metastatic lymph nodes by a lymphatic drug delivery system with 5‐fluorouracil |
title | Treatment of false‐negative metastatic lymph nodes by a lymphatic drug delivery system with 5‐fluorouracil |
title_full | Treatment of false‐negative metastatic lymph nodes by a lymphatic drug delivery system with 5‐fluorouracil |
title_fullStr | Treatment of false‐negative metastatic lymph nodes by a lymphatic drug delivery system with 5‐fluorouracil |
title_full_unstemmed | Treatment of false‐negative metastatic lymph nodes by a lymphatic drug delivery system with 5‐fluorouracil |
title_short | Treatment of false‐negative metastatic lymph nodes by a lymphatic drug delivery system with 5‐fluorouracil |
title_sort | treatment of false‐negative metastatic lymph nodes by a lymphatic drug delivery system with 5‐fluorouracil |
topic | Clinical Cancer Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6536938/ https://www.ncbi.nlm.nih.gov/pubmed/30945479 http://dx.doi.org/10.1002/cam4.2125 |
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