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Gene amplification of YB‐1 in castration‐resistant prostate cancer in association with aberrant androgen receptor expression

Although Y‐box binding protein‐1 (YB‐1) is known to be overexpressed in prostate cancer, especially castration‐resistant prostate cancer (CRPC), the mechanism of its overexpression remains unclear. We aimed to elucidate the mechanism of YB‐1 overexpression in CRPC. Gene amplification in CRPC cells a...

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Autores principales: Shiota, Masaki, Sekino, Yohei, Tsukahara, Shigehiro, Abe, Tatsuro, Kinoshita, Fumio, Imada, Kenjiro, Ueda, Shohei, Ushijima, Miho, Nagakawa, Shohei, Matsumoto, Takashi, Kashiwagi, Eiji, Takeuchi, Ario, Inokuchi, Junichi, Uchiumi, Takeshi, Oda, Yoshinao, Eto, Masatoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7780013/
https://www.ncbi.nlm.nih.gov/pubmed/33064355
http://dx.doi.org/10.1111/cas.14695
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author Shiota, Masaki
Sekino, Yohei
Tsukahara, Shigehiro
Abe, Tatsuro
Kinoshita, Fumio
Imada, Kenjiro
Ueda, Shohei
Ushijima, Miho
Nagakawa, Shohei
Matsumoto, Takashi
Kashiwagi, Eiji
Takeuchi, Ario
Inokuchi, Junichi
Uchiumi, Takeshi
Oda, Yoshinao
Eto, Masatoshi
author_facet Shiota, Masaki
Sekino, Yohei
Tsukahara, Shigehiro
Abe, Tatsuro
Kinoshita, Fumio
Imada, Kenjiro
Ueda, Shohei
Ushijima, Miho
Nagakawa, Shohei
Matsumoto, Takashi
Kashiwagi, Eiji
Takeuchi, Ario
Inokuchi, Junichi
Uchiumi, Takeshi
Oda, Yoshinao
Eto, Masatoshi
author_sort Shiota, Masaki
collection PubMed
description Although Y‐box binding protein‐1 (YB‐1) is known to be overexpressed in prostate cancer, especially castration‐resistant prostate cancer (CRPC), the mechanism of its overexpression remains unclear. We aimed to elucidate the mechanism of YB‐1 overexpression in CRPC. Gene amplification in CRPC cells and tissues was examined by public database analysis, and digital PCR. The significance of YB‐1 amplification for the YB‐1/androgen receptor (AR) axis and prognosis was examined by public database analysis and immunohistochemistry. YB‐1 amplification was mainly observed in CRPC tissues by public database analysis and confirmed in CRPC cells and tissues by digital PCR. Expression of YB‐1 was increased in CRPC tissues compared with treatment‐naïve tissues. Furthermore, YB‐1 and phosphorylated YB‐1 levels were associated with AR and AR V7 expression levels. Finally, YB‐1 amplification was associated with poor outcomes in CRPC. Taken together, the present findings suggest that YB‐1 amplification contributes to progression to CRPC through regulation of AR and AR V7 expressions, and that YB‐1 is a promising therapeutic target in CRPC.
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spelling pubmed-77800132021-01-08 Gene amplification of YB‐1 in castration‐resistant prostate cancer in association with aberrant androgen receptor expression Shiota, Masaki Sekino, Yohei Tsukahara, Shigehiro Abe, Tatsuro Kinoshita, Fumio Imada, Kenjiro Ueda, Shohei Ushijima, Miho Nagakawa, Shohei Matsumoto, Takashi Kashiwagi, Eiji Takeuchi, Ario Inokuchi, Junichi Uchiumi, Takeshi Oda, Yoshinao Eto, Masatoshi Cancer Sci Clinical Research Although Y‐box binding protein‐1 (YB‐1) is known to be overexpressed in prostate cancer, especially castration‐resistant prostate cancer (CRPC), the mechanism of its overexpression remains unclear. We aimed to elucidate the mechanism of YB‐1 overexpression in CRPC. Gene amplification in CRPC cells and tissues was examined by public database analysis, and digital PCR. The significance of YB‐1 amplification for the YB‐1/androgen receptor (AR) axis and prognosis was examined by public database analysis and immunohistochemistry. YB‐1 amplification was mainly observed in CRPC tissues by public database analysis and confirmed in CRPC cells and tissues by digital PCR. Expression of YB‐1 was increased in CRPC tissues compared with treatment‐naïve tissues. Furthermore, YB‐1 and phosphorylated YB‐1 levels were associated with AR and AR V7 expression levels. Finally, YB‐1 amplification was associated with poor outcomes in CRPC. Taken together, the present findings suggest that YB‐1 amplification contributes to progression to CRPC through regulation of AR and AR V7 expressions, and that YB‐1 is a promising therapeutic target in CRPC. John Wiley and Sons Inc. 2020-11-24 2021-01 /pmc/articles/PMC7780013/ /pubmed/33064355 http://dx.doi.org/10.1111/cas.14695 Text en © 2020 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 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 Clinical Research
Shiota, Masaki
Sekino, Yohei
Tsukahara, Shigehiro
Abe, Tatsuro
Kinoshita, Fumio
Imada, Kenjiro
Ueda, Shohei
Ushijima, Miho
Nagakawa, Shohei
Matsumoto, Takashi
Kashiwagi, Eiji
Takeuchi, Ario
Inokuchi, Junichi
Uchiumi, Takeshi
Oda, Yoshinao
Eto, Masatoshi
Gene amplification of YB‐1 in castration‐resistant prostate cancer in association with aberrant androgen receptor expression
title Gene amplification of YB‐1 in castration‐resistant prostate cancer in association with aberrant androgen receptor expression
title_full Gene amplification of YB‐1 in castration‐resistant prostate cancer in association with aberrant androgen receptor expression
title_fullStr Gene amplification of YB‐1 in castration‐resistant prostate cancer in association with aberrant androgen receptor expression
title_full_unstemmed Gene amplification of YB‐1 in castration‐resistant prostate cancer in association with aberrant androgen receptor expression
title_short Gene amplification of YB‐1 in castration‐resistant prostate cancer in association with aberrant androgen receptor expression
title_sort gene amplification of yb‐1 in castration‐resistant prostate cancer in association with aberrant androgen receptor expression
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7780013/
https://www.ncbi.nlm.nih.gov/pubmed/33064355
http://dx.doi.org/10.1111/cas.14695
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