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Synergistic anti-tumor effects of arsenic trioxide and blue LED irradiation on human osteosarcoma
Arsenic trioxide (ATO) has been well recognized as an anti-tumor agent for various human cancers. Recently, the blue light emitting diodes (LEDs)-based therapy has also been demonstrated to be potential therapeutic strategies for several cancers. However, the combination effects of ATO and blue LED...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6367547/ https://www.ncbi.nlm.nih.gov/pubmed/30745828 http://dx.doi.org/10.7150/ijbs.28356 |
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author | Feng, Chao Gong, Rui Zheng, Qiuyan Yan, Gege He, Mingyu Lei, Hong Li, Xingda Zhang, Lai Xu, Zihang Liu, Shenzhen Yu, Meixi Ma, Tianshuai Gao, Manqi Bamba, Djibril Idiiatullina, Elina Zagidullin, Naufal Pavlov, Valentin Xu, Chaoqian Yuan, Ye Yang, Lei |
author_facet | Feng, Chao Gong, Rui Zheng, Qiuyan Yan, Gege He, Mingyu Lei, Hong Li, Xingda Zhang, Lai Xu, Zihang Liu, Shenzhen Yu, Meixi Ma, Tianshuai Gao, Manqi Bamba, Djibril Idiiatullina, Elina Zagidullin, Naufal Pavlov, Valentin Xu, Chaoqian Yuan, Ye Yang, Lei |
author_sort | Feng, Chao |
collection | PubMed |
description | Arsenic trioxide (ATO) has been well recognized as an anti-tumor agent for various human cancers. Recently, the blue light emitting diodes (LEDs)-based therapy has also been demonstrated to be potential therapeutic strategies for several cancers. However, the combination effects of ATO and blue LED on tumor suppression are still unclear. In this study, we determined whether combination of ATO and blue LED irradiation at 470 nm in wavelength exhibited superior anti-tumor activity in human osteosarcoma (OS). We observed that combination treatments of ATO and blue LED much more significantly decreased the percentages of proliferative cells, and increased apoptotic rate compared with any single treatments in U-2 OS cells. Furthermore, we found suppression of cell migration and invasion were much more pronounced in ATO plus blue LED treated group than single treated groups. Moreover, reactive oxygen species (ROS) assay and immunostaining of γ-H2A.X and p53 indicated that the combined treatments resulted in further markedly increases in ROS accumulation, DNA damage and p53 activity. Taken together, our study demonstrated synergistical anti-tumor effects of combined treatments of ATO and blue LED on human OS cells, which were associated with an increased ROS accumulation, DNA damaged mediated p53 activation. |
format | Online Article Text |
id | pubmed-6367547 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-63675472019-02-11 Synergistic anti-tumor effects of arsenic trioxide and blue LED irradiation on human osteosarcoma Feng, Chao Gong, Rui Zheng, Qiuyan Yan, Gege He, Mingyu Lei, Hong Li, Xingda Zhang, Lai Xu, Zihang Liu, Shenzhen Yu, Meixi Ma, Tianshuai Gao, Manqi Bamba, Djibril Idiiatullina, Elina Zagidullin, Naufal Pavlov, Valentin Xu, Chaoqian Yuan, Ye Yang, Lei Int J Biol Sci Research Paper Arsenic trioxide (ATO) has been well recognized as an anti-tumor agent for various human cancers. Recently, the blue light emitting diodes (LEDs)-based therapy has also been demonstrated to be potential therapeutic strategies for several cancers. However, the combination effects of ATO and blue LED on tumor suppression are still unclear. In this study, we determined whether combination of ATO and blue LED irradiation at 470 nm in wavelength exhibited superior anti-tumor activity in human osteosarcoma (OS). We observed that combination treatments of ATO and blue LED much more significantly decreased the percentages of proliferative cells, and increased apoptotic rate compared with any single treatments in U-2 OS cells. Furthermore, we found suppression of cell migration and invasion were much more pronounced in ATO plus blue LED treated group than single treated groups. Moreover, reactive oxygen species (ROS) assay and immunostaining of γ-H2A.X and p53 indicated that the combined treatments resulted in further markedly increases in ROS accumulation, DNA damage and p53 activity. Taken together, our study demonstrated synergistical anti-tumor effects of combined treatments of ATO and blue LED on human OS cells, which were associated with an increased ROS accumulation, DNA damaged mediated p53 activation. Ivyspring International Publisher 2019-01-01 /pmc/articles/PMC6367547/ /pubmed/30745828 http://dx.doi.org/10.7150/ijbs.28356 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Feng, Chao Gong, Rui Zheng, Qiuyan Yan, Gege He, Mingyu Lei, Hong Li, Xingda Zhang, Lai Xu, Zihang Liu, Shenzhen Yu, Meixi Ma, Tianshuai Gao, Manqi Bamba, Djibril Idiiatullina, Elina Zagidullin, Naufal Pavlov, Valentin Xu, Chaoqian Yuan, Ye Yang, Lei Synergistic anti-tumor effects of arsenic trioxide and blue LED irradiation on human osteosarcoma |
title | Synergistic anti-tumor effects of arsenic trioxide and blue LED irradiation on human osteosarcoma |
title_full | Synergistic anti-tumor effects of arsenic trioxide and blue LED irradiation on human osteosarcoma |
title_fullStr | Synergistic anti-tumor effects of arsenic trioxide and blue LED irradiation on human osteosarcoma |
title_full_unstemmed | Synergistic anti-tumor effects of arsenic trioxide and blue LED irradiation on human osteosarcoma |
title_short | Synergistic anti-tumor effects of arsenic trioxide and blue LED irradiation on human osteosarcoma |
title_sort | synergistic anti-tumor effects of arsenic trioxide and blue led irradiation on human osteosarcoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6367547/ https://www.ncbi.nlm.nih.gov/pubmed/30745828 http://dx.doi.org/10.7150/ijbs.28356 |
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