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Protein kinase A inhibition facilitates the antitumor activity of xanthohumol, a valosin‐containing protein inhibitor
Xanthohumol (XN), a simple prenylated chalcone, can be isolated from hops and has the potential to be a cancer chemopreventive agent against several human tumor cell lines. We previously identified valosin‐containing protein (VCP) as a target of XN; VCP can also play crucial roles in cancer progress...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5406609/ https://www.ncbi.nlm.nih.gov/pubmed/28122154 http://dx.doi.org/10.1111/cas.13175 |
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author | Shikata, Yuki Yoshimaru, Tetsuro Komatsu, Masato Katoh, Hiroto Sato, Reiko Kanagaki, Shuhei Okazaki, Yasumasa Toyokuni, Shinya Tashiro, Etsu Ishikawa, Shumpei Katagiri, Toyomasa Imoto, Masaya |
author_facet | Shikata, Yuki Yoshimaru, Tetsuro Komatsu, Masato Katoh, Hiroto Sato, Reiko Kanagaki, Shuhei Okazaki, Yasumasa Toyokuni, Shinya Tashiro, Etsu Ishikawa, Shumpei Katagiri, Toyomasa Imoto, Masaya |
author_sort | Shikata, Yuki |
collection | PubMed |
description | Xanthohumol (XN), a simple prenylated chalcone, can be isolated from hops and has the potential to be a cancer chemopreventive agent against several human tumor cell lines. We previously identified valosin‐containing protein (VCP) as a target of XN; VCP can also play crucial roles in cancer progression and prognosis. Therefore, we investigated the molecular mechanisms governing the contribution of VCP to the antitumor activity of XN. Several human tumor cell lines were treated with XN to investigate which human tumor cell lines are sensitive to XN. Several cell lines exhibited high sensitivity to XN both in vitro and in vivo. shRNA screening and bioinformatics analysis identified that the inhibition of the adenylate cyclase (AC) pathway synergistically facilitated apoptosis induced by VCP inhibition. These results suggest that there is crosstalk between the AC pathway and VCP function, and targeting both VCP and the AC pathway is a potential chemotherapeutic strategy for a subset of tumor cells. |
format | Online Article Text |
id | pubmed-5406609 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54066092017-05-01 Protein kinase A inhibition facilitates the antitumor activity of xanthohumol, a valosin‐containing protein inhibitor Shikata, Yuki Yoshimaru, Tetsuro Komatsu, Masato Katoh, Hiroto Sato, Reiko Kanagaki, Shuhei Okazaki, Yasumasa Toyokuni, Shinya Tashiro, Etsu Ishikawa, Shumpei Katagiri, Toyomasa Imoto, Masaya Cancer Sci Original Articles Xanthohumol (XN), a simple prenylated chalcone, can be isolated from hops and has the potential to be a cancer chemopreventive agent against several human tumor cell lines. We previously identified valosin‐containing protein (VCP) as a target of XN; VCP can also play crucial roles in cancer progression and prognosis. Therefore, we investigated the molecular mechanisms governing the contribution of VCP to the antitumor activity of XN. Several human tumor cell lines were treated with XN to investigate which human tumor cell lines are sensitive to XN. Several cell lines exhibited high sensitivity to XN both in vitro and in vivo. shRNA screening and bioinformatics analysis identified that the inhibition of the adenylate cyclase (AC) pathway synergistically facilitated apoptosis induced by VCP inhibition. These results suggest that there is crosstalk between the AC pathway and VCP function, and targeting both VCP and the AC pathway is a potential chemotherapeutic strategy for a subset of tumor cells. John Wiley and Sons Inc. 2017-04-20 2017-04 /pmc/articles/PMC5406609/ /pubmed/28122154 http://dx.doi.org/10.1111/cas.13175 Text en © 2017 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Shikata, Yuki Yoshimaru, Tetsuro Komatsu, Masato Katoh, Hiroto Sato, Reiko Kanagaki, Shuhei Okazaki, Yasumasa Toyokuni, Shinya Tashiro, Etsu Ishikawa, Shumpei Katagiri, Toyomasa Imoto, Masaya Protein kinase A inhibition facilitates the antitumor activity of xanthohumol, a valosin‐containing protein inhibitor |
title | Protein kinase A inhibition facilitates the antitumor activity of xanthohumol, a valosin‐containing protein inhibitor |
title_full | Protein kinase A inhibition facilitates the antitumor activity of xanthohumol, a valosin‐containing protein inhibitor |
title_fullStr | Protein kinase A inhibition facilitates the antitumor activity of xanthohumol, a valosin‐containing protein inhibitor |
title_full_unstemmed | Protein kinase A inhibition facilitates the antitumor activity of xanthohumol, a valosin‐containing protein inhibitor |
title_short | Protein kinase A inhibition facilitates the antitumor activity of xanthohumol, a valosin‐containing protein inhibitor |
title_sort | protein kinase a inhibition facilitates the antitumor activity of xanthohumol, a valosin‐containing protein inhibitor |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5406609/ https://www.ncbi.nlm.nih.gov/pubmed/28122154 http://dx.doi.org/10.1111/cas.13175 |
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