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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...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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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. |
format | Online Article Text |
id | pubmed-7780013 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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