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Acridine orange exhibits photodamage in human bladder cancer cells under blue light exposure

Human bladder cancer (BC) cells exhibit a high basal level of autophagic activity with accumulation of acridine-orange(AO)-stained acidic vesicular organelles. The rapid AO relocalization was observed in treated BC cells under blue-light emission. To investigate the cytotoxic effects of AO on human...

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Autores principales: Lin, Yi-Chia, Lin, Ji-Fan, Tsai, Te-Fu, Chen, Hung-En, Chou, Kuang-Yu, Yang, Shan-Che, Tang, Ya-Ming, Hwang, Thomas I.-Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658329/
https://www.ncbi.nlm.nih.gov/pubmed/29074848
http://dx.doi.org/10.1038/s41598-017-13904-0
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author Lin, Yi-Chia
Lin, Ji-Fan
Tsai, Te-Fu
Chen, Hung-En
Chou, Kuang-Yu
Yang, Shan-Che
Tang, Ya-Ming
Hwang, Thomas I.-Sheng
author_facet Lin, Yi-Chia
Lin, Ji-Fan
Tsai, Te-Fu
Chen, Hung-En
Chou, Kuang-Yu
Yang, Shan-Che
Tang, Ya-Ming
Hwang, Thomas I.-Sheng
author_sort Lin, Yi-Chia
collection PubMed
description Human bladder cancer (BC) cells exhibit a high basal level of autophagic activity with accumulation of acridine-orange(AO)-stained acidic vesicular organelles. The rapid AO relocalization was observed in treated BC cells under blue-light emission. To investigate the cytotoxic effects of AO on human BC cell lines under blue-light exposure, human immortalized uroepithelial (SV-Huc-1) and BC cell lines (5637 and T24) were treated with indicated concentrations of AO or blue-light exposure alone and in combination. The cell viability was then determined using WST-1, time-lapse imaging with a Cytosmart System and continuous quantification with a multi-mode image-based reader. Treatment of AO or blue-light exposure alone did not cause a significant loss of viability in BC cells. However, AO exhibited a dose-dependent increment of cytotoxicity toward BC cells under blue-light exposure. Furthermore, the tumor formation of BC cells with treatment was significantly reduced when evaluated in a mouse xenograft model. The photodamage caused by AO was nearly neglected in SV-Huc-1 cells, suggesting a differential effect of this treatment between cancer and normal cells. In summary, AO, as a photosensitizer, disrupts acidic organelles and induces cancer cell death in BC cells under blue-light irradiation. Our findings may serve as a novel therapeutic strategy against human BC.
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spelling pubmed-56583292017-10-31 Acridine orange exhibits photodamage in human bladder cancer cells under blue light exposure Lin, Yi-Chia Lin, Ji-Fan Tsai, Te-Fu Chen, Hung-En Chou, Kuang-Yu Yang, Shan-Che Tang, Ya-Ming Hwang, Thomas I.-Sheng Sci Rep Article Human bladder cancer (BC) cells exhibit a high basal level of autophagic activity with accumulation of acridine-orange(AO)-stained acidic vesicular organelles. The rapid AO relocalization was observed in treated BC cells under blue-light emission. To investigate the cytotoxic effects of AO on human BC cell lines under blue-light exposure, human immortalized uroepithelial (SV-Huc-1) and BC cell lines (5637 and T24) were treated with indicated concentrations of AO or blue-light exposure alone and in combination. The cell viability was then determined using WST-1, time-lapse imaging with a Cytosmart System and continuous quantification with a multi-mode image-based reader. Treatment of AO or blue-light exposure alone did not cause a significant loss of viability in BC cells. However, AO exhibited a dose-dependent increment of cytotoxicity toward BC cells under blue-light exposure. Furthermore, the tumor formation of BC cells with treatment was significantly reduced when evaluated in a mouse xenograft model. The photodamage caused by AO was nearly neglected in SV-Huc-1 cells, suggesting a differential effect of this treatment between cancer and normal cells. In summary, AO, as a photosensitizer, disrupts acidic organelles and induces cancer cell death in BC cells under blue-light irradiation. Our findings may serve as a novel therapeutic strategy against human BC. Nature Publishing Group UK 2017-10-26 /pmc/articles/PMC5658329/ /pubmed/29074848 http://dx.doi.org/10.1038/s41598-017-13904-0 Text en © The Author(s) 2017 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
Lin, Yi-Chia
Lin, Ji-Fan
Tsai, Te-Fu
Chen, Hung-En
Chou, Kuang-Yu
Yang, Shan-Che
Tang, Ya-Ming
Hwang, Thomas I.-Sheng
Acridine orange exhibits photodamage in human bladder cancer cells under blue light exposure
title Acridine orange exhibits photodamage in human bladder cancer cells under blue light exposure
title_full Acridine orange exhibits photodamage in human bladder cancer cells under blue light exposure
title_fullStr Acridine orange exhibits photodamage in human bladder cancer cells under blue light exposure
title_full_unstemmed Acridine orange exhibits photodamage in human bladder cancer cells under blue light exposure
title_short Acridine orange exhibits photodamage in human bladder cancer cells under blue light exposure
title_sort acridine orange exhibits photodamage in human bladder cancer cells under blue light exposure
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658329/
https://www.ncbi.nlm.nih.gov/pubmed/29074848
http://dx.doi.org/10.1038/s41598-017-13904-0
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