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Photoactivatable oncolytic adenovirus for optogenetic cancer therapy

Virotherapy using oncolytic adenovirus is an effective anticancer strategy. However, the tumor selectivity of oncolytic adenoviruses is not enough high. To develop oncolytic adenovirus with a low risk of off-tumor toxicity, we constructed a photoactivatable oncolytic adenovirus (paOAd). In response...

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Autores principales: Hagihara, Yasuko, Sakamoto, Ayaka, Tokuda, Takashi, Yamashita, Tomoki, Ikemoto, Sena, Kimura, Ayaka, Haruta, Makito, Sasagawa, Kiyotaka, Ohta, Jun, Takayama, Kazuo, Mizuguchi, Hiroyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7378209/
https://www.ncbi.nlm.nih.gov/pubmed/32703933
http://dx.doi.org/10.1038/s41419-020-02782-6
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author Hagihara, Yasuko
Sakamoto, Ayaka
Tokuda, Takashi
Yamashita, Tomoki
Ikemoto, Sena
Kimura, Ayaka
Haruta, Makito
Sasagawa, Kiyotaka
Ohta, Jun
Takayama, Kazuo
Mizuguchi, Hiroyuki
author_facet Hagihara, Yasuko
Sakamoto, Ayaka
Tokuda, Takashi
Yamashita, Tomoki
Ikemoto, Sena
Kimura, Ayaka
Haruta, Makito
Sasagawa, Kiyotaka
Ohta, Jun
Takayama, Kazuo
Mizuguchi, Hiroyuki
author_sort Hagihara, Yasuko
collection PubMed
description Virotherapy using oncolytic adenovirus is an effective anticancer strategy. However, the tumor selectivity of oncolytic adenoviruses is not enough high. To develop oncolytic adenovirus with a low risk of off-tumor toxicity, we constructed a photoactivatable oncolytic adenovirus (paOAd). In response to blue light irradiation, the expression of adenoviral E1 genes, which are necessary for adenoviral replication, is induced and replication of this adenovirus occurs. In vitro, efficient lysis of various human cancer cell lines was observed by paOAd infection followed by blue light irradiation. Importantly, there was no off-tumor toxicity unless the cells were irradiated by blue light. In vivo, tumor growth in a subcutaneous tumor model and a mouse model of liver cancer was significantly inhibited by paOAd infection followed by blue light irradiation. In addition, paOAd also showed a therapeutic effect on cancer stem cells. These results suggest that paOAd is useful as a safe and therapeutically effective cancer therapy.
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spelling pubmed-73782092020-07-24 Photoactivatable oncolytic adenovirus for optogenetic cancer therapy Hagihara, Yasuko Sakamoto, Ayaka Tokuda, Takashi Yamashita, Tomoki Ikemoto, Sena Kimura, Ayaka Haruta, Makito Sasagawa, Kiyotaka Ohta, Jun Takayama, Kazuo Mizuguchi, Hiroyuki Cell Death Dis Article Virotherapy using oncolytic adenovirus is an effective anticancer strategy. However, the tumor selectivity of oncolytic adenoviruses is not enough high. To develop oncolytic adenovirus with a low risk of off-tumor toxicity, we constructed a photoactivatable oncolytic adenovirus (paOAd). In response to blue light irradiation, the expression of adenoviral E1 genes, which are necessary for adenoviral replication, is induced and replication of this adenovirus occurs. In vitro, efficient lysis of various human cancer cell lines was observed by paOAd infection followed by blue light irradiation. Importantly, there was no off-tumor toxicity unless the cells were irradiated by blue light. In vivo, tumor growth in a subcutaneous tumor model and a mouse model of liver cancer was significantly inhibited by paOAd infection followed by blue light irradiation. In addition, paOAd also showed a therapeutic effect on cancer stem cells. These results suggest that paOAd is useful as a safe and therapeutically effective cancer therapy. Nature Publishing Group UK 2020-07-23 /pmc/articles/PMC7378209/ /pubmed/32703933 http://dx.doi.org/10.1038/s41419-020-02782-6 Text en © The Author(s) 2020 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
Hagihara, Yasuko
Sakamoto, Ayaka
Tokuda, Takashi
Yamashita, Tomoki
Ikemoto, Sena
Kimura, Ayaka
Haruta, Makito
Sasagawa, Kiyotaka
Ohta, Jun
Takayama, Kazuo
Mizuguchi, Hiroyuki
Photoactivatable oncolytic adenovirus for optogenetic cancer therapy
title Photoactivatable oncolytic adenovirus for optogenetic cancer therapy
title_full Photoactivatable oncolytic adenovirus for optogenetic cancer therapy
title_fullStr Photoactivatable oncolytic adenovirus for optogenetic cancer therapy
title_full_unstemmed Photoactivatable oncolytic adenovirus for optogenetic cancer therapy
title_short Photoactivatable oncolytic adenovirus for optogenetic cancer therapy
title_sort photoactivatable oncolytic adenovirus for optogenetic cancer therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7378209/
https://www.ncbi.nlm.nih.gov/pubmed/32703933
http://dx.doi.org/10.1038/s41419-020-02782-6
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