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Effects of a monoclonal antibody against (pro)renin receptor on gliomagenesis

Glioblastoma is characterized by a strong self-renewal potential and poor differentiated state. We have reported previously that the (pro)renin receptor [(P)RR] is a potential target for glioma therapy by silencing the (P)RR gene. Here, we have examined the effects of a monoclonal antibody against (...

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Autores principales: Fujimori, Takeshi, Shibayama, Yuki, Kanda, Takahiro, Suzuki, Kenta, Ogawa, Daisuke, Ishikawa, Ryou, Kadota, Kyuichi, Matsunaga, Toru, Tamiya, Takashi, Nishiyama, Akira, Miyake, Keisuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842725/
https://www.ncbi.nlm.nih.gov/pubmed/36646875
http://dx.doi.org/10.1038/s41598-023-28133-x
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author Fujimori, Takeshi
Shibayama, Yuki
Kanda, Takahiro
Suzuki, Kenta
Ogawa, Daisuke
Ishikawa, Ryou
Kadota, Kyuichi
Matsunaga, Toru
Tamiya, Takashi
Nishiyama, Akira
Miyake, Keisuke
author_facet Fujimori, Takeshi
Shibayama, Yuki
Kanda, Takahiro
Suzuki, Kenta
Ogawa, Daisuke
Ishikawa, Ryou
Kadota, Kyuichi
Matsunaga, Toru
Tamiya, Takashi
Nishiyama, Akira
Miyake, Keisuke
author_sort Fujimori, Takeshi
collection PubMed
description Glioblastoma is characterized by a strong self-renewal potential and poor differentiated state. We have reported previously that the (pro)renin receptor [(P)RR] is a potential target for glioma therapy by silencing the (P)RR gene. Here, we have examined the effects of a monoclonal antibody against (P)RR on gliomagenesis. Human glioma cell lines (U251MG and U87MG) and a glioma stem cell line (MGG23) were used for the in vitro study. The expressions of the Wnt/β-catenin signaling pathway (Wnt signaling pathway) components and stemness markers were measured by Western blotting. The effects of the (P)RR antibody on cell proliferation, sphere formation, apoptosis and migration were also examined. Subcutaneous xenografts were also examined in nude mice. Treatment with the (P)RR antibody reduced expression of Wnt signaling pathway components and stemness markers. Furthermore, the (P)RR antibody reduced cell proliferation and decreased sphere formation significantly. The treatment also suppressed migration and induced apoptosis. In a subcutaneous xenograft model, systemic administration of the (P)RR antibody reduced tumor volume significantly. These data show that treatment with the (P)RR antibody is a potential therapeutic strategy for treating glioblastoma.
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spelling pubmed-98427252023-01-18 Effects of a monoclonal antibody against (pro)renin receptor on gliomagenesis Fujimori, Takeshi Shibayama, Yuki Kanda, Takahiro Suzuki, Kenta Ogawa, Daisuke Ishikawa, Ryou Kadota, Kyuichi Matsunaga, Toru Tamiya, Takashi Nishiyama, Akira Miyake, Keisuke Sci Rep Article Glioblastoma is characterized by a strong self-renewal potential and poor differentiated state. We have reported previously that the (pro)renin receptor [(P)RR] is a potential target for glioma therapy by silencing the (P)RR gene. Here, we have examined the effects of a monoclonal antibody against (P)RR on gliomagenesis. Human glioma cell lines (U251MG and U87MG) and a glioma stem cell line (MGG23) were used for the in vitro study. The expressions of the Wnt/β-catenin signaling pathway (Wnt signaling pathway) components and stemness markers were measured by Western blotting. The effects of the (P)RR antibody on cell proliferation, sphere formation, apoptosis and migration were also examined. Subcutaneous xenografts were also examined in nude mice. Treatment with the (P)RR antibody reduced expression of Wnt signaling pathway components and stemness markers. Furthermore, the (P)RR antibody reduced cell proliferation and decreased sphere formation significantly. The treatment also suppressed migration and induced apoptosis. In a subcutaneous xenograft model, systemic administration of the (P)RR antibody reduced tumor volume significantly. These data show that treatment with the (P)RR antibody is a potential therapeutic strategy for treating glioblastoma. Nature Publishing Group UK 2023-01-16 /pmc/articles/PMC9842725/ /pubmed/36646875 http://dx.doi.org/10.1038/s41598-023-28133-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Fujimori, Takeshi
Shibayama, Yuki
Kanda, Takahiro
Suzuki, Kenta
Ogawa, Daisuke
Ishikawa, Ryou
Kadota, Kyuichi
Matsunaga, Toru
Tamiya, Takashi
Nishiyama, Akira
Miyake, Keisuke
Effects of a monoclonal antibody against (pro)renin receptor on gliomagenesis
title Effects of a monoclonal antibody against (pro)renin receptor on gliomagenesis
title_full Effects of a monoclonal antibody against (pro)renin receptor on gliomagenesis
title_fullStr Effects of a monoclonal antibody against (pro)renin receptor on gliomagenesis
title_full_unstemmed Effects of a monoclonal antibody against (pro)renin receptor on gliomagenesis
title_short Effects of a monoclonal antibody against (pro)renin receptor on gliomagenesis
title_sort effects of a monoclonal antibody against (pro)renin receptor on gliomagenesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842725/
https://www.ncbi.nlm.nih.gov/pubmed/36646875
http://dx.doi.org/10.1038/s41598-023-28133-x
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