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Efficacy of 5-aminolevulinic acid-mediated photodynamic therapy in a mouse model of esophageal cancer
5-Aminolevulinic acid-mediated photodynamic therapy (ALA-PDT) is a minimally invasive therapeutic modality used in the management of various cancers, but to a lesser extent for esophageal cancer (EC). The current study investigated the antitumor effects of ALA-PDT. Human EC cells were treated with A...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7436933/ https://www.ncbi.nlm.nih.gov/pubmed/32863915 http://dx.doi.org/10.3892/ol.2020.11943 |
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author | Tanaka, Yoshihiro Murayama, Yasutoshi Matsumoto, Tatsuya Kubo, Hidemasa Harada, Kyoichi Matsuo, Hisataka Kubota, Takeshi Okamoto, Kazuma Otsuji, Eigo |
author_facet | Tanaka, Yoshihiro Murayama, Yasutoshi Matsumoto, Tatsuya Kubo, Hidemasa Harada, Kyoichi Matsuo, Hisataka Kubota, Takeshi Okamoto, Kazuma Otsuji, Eigo |
author_sort | Tanaka, Yoshihiro |
collection | PubMed |
description | 5-Aminolevulinic acid-mediated photodynamic therapy (ALA-PDT) is a minimally invasive therapeutic modality used in the management of various cancers, but to a lesser extent for esophageal cancer (EC). The current study investigated the antitumor effects of ALA-PDT. Human EC cells were treated with ALA, after which ALA-induced fluorescence was examined under a fluorescence microscope. The cytotoxic effects of ALA-PDT were assessed using three types of LEDs (blue, green and red) in vitro and in vivo. Subcutaneous tumor model mice was constructed with KYSE150 cells. ALA-PDT was performed once a week for 4 weeks and tumor weights were measured. A popliteal lymph node (PLN) metastasis murine model was generated using KYSE150 cells. KYSE150 cells were inoculated into the left footpad of nude mice. ALA-PDT was performed on the footpad once a week for 4 weeks. PLNs were then removed 3 weeks after the last treatment. The lymph nodes were evaluated by hematoxylin and eosin staining. Red fluorescence of protoporphyrin IX (PpIX) was observed in all EC cell lines. ALA-PDT using LEDs exerted significant antitumor effects in vitro and in vivo. The antitumor effects of ALA-PDT with blue LED were the strongest, followed by green and red LEDs. The number of metastasized PLNs was significantly smaller in the ALA-PDT group (0%) than in the control group (37.5%). The present results indicated that ALA-PDT is effective for EC. |
format | Online Article Text |
id | pubmed-7436933 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-74369332020-08-27 Efficacy of 5-aminolevulinic acid-mediated photodynamic therapy in a mouse model of esophageal cancer Tanaka, Yoshihiro Murayama, Yasutoshi Matsumoto, Tatsuya Kubo, Hidemasa Harada, Kyoichi Matsuo, Hisataka Kubota, Takeshi Okamoto, Kazuma Otsuji, Eigo Oncol Lett Articles 5-Aminolevulinic acid-mediated photodynamic therapy (ALA-PDT) is a minimally invasive therapeutic modality used in the management of various cancers, but to a lesser extent for esophageal cancer (EC). The current study investigated the antitumor effects of ALA-PDT. Human EC cells were treated with ALA, after which ALA-induced fluorescence was examined under a fluorescence microscope. The cytotoxic effects of ALA-PDT were assessed using three types of LEDs (blue, green and red) in vitro and in vivo. Subcutaneous tumor model mice was constructed with KYSE150 cells. ALA-PDT was performed once a week for 4 weeks and tumor weights were measured. A popliteal lymph node (PLN) metastasis murine model was generated using KYSE150 cells. KYSE150 cells were inoculated into the left footpad of nude mice. ALA-PDT was performed on the footpad once a week for 4 weeks. PLNs were then removed 3 weeks after the last treatment. The lymph nodes were evaluated by hematoxylin and eosin staining. Red fluorescence of protoporphyrin IX (PpIX) was observed in all EC cell lines. ALA-PDT using LEDs exerted significant antitumor effects in vitro and in vivo. The antitumor effects of ALA-PDT with blue LED were the strongest, followed by green and red LEDs. The number of metastasized PLNs was significantly smaller in the ALA-PDT group (0%) than in the control group (37.5%). The present results indicated that ALA-PDT is effective for EC. D.A. Spandidos 2020-10 2020-08-04 /pmc/articles/PMC7436933/ /pubmed/32863915 http://dx.doi.org/10.3892/ol.2020.11943 Text en Copyright: © Tanaka et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Tanaka, Yoshihiro Murayama, Yasutoshi Matsumoto, Tatsuya Kubo, Hidemasa Harada, Kyoichi Matsuo, Hisataka Kubota, Takeshi Okamoto, Kazuma Otsuji, Eigo Efficacy of 5-aminolevulinic acid-mediated photodynamic therapy in a mouse model of esophageal cancer |
title | Efficacy of 5-aminolevulinic acid-mediated photodynamic therapy in a mouse model of esophageal cancer |
title_full | Efficacy of 5-aminolevulinic acid-mediated photodynamic therapy in a mouse model of esophageal cancer |
title_fullStr | Efficacy of 5-aminolevulinic acid-mediated photodynamic therapy in a mouse model of esophageal cancer |
title_full_unstemmed | Efficacy of 5-aminolevulinic acid-mediated photodynamic therapy in a mouse model of esophageal cancer |
title_short | Efficacy of 5-aminolevulinic acid-mediated photodynamic therapy in a mouse model of esophageal cancer |
title_sort | efficacy of 5-aminolevulinic acid-mediated photodynamic therapy in a mouse model of esophageal cancer |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7436933/ https://www.ncbi.nlm.nih.gov/pubmed/32863915 http://dx.doi.org/10.3892/ol.2020.11943 |
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