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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...

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Autores principales: Shikata, Yuki, Yoshimaru, Tetsuro, Komatsu, Masato, Katoh, Hiroto, Sato, Reiko, Kanagaki, Shuhei, Okazaki, Yasumasa, Toyokuni, Shinya, Tashiro, Etsu, Ishikawa, Shumpei, Katagiri, Toyomasa, Imoto, Masaya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
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.
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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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