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CLDN8, an androgen‐regulated gene, promotes prostate cancer cell proliferation and migration
The proliferation of prostate cancer cells is controlled by the androgen receptor (AR) signaling pathway. However, the function of AR target genes has not been fully elucidated. In previous studies, we have identified global AR binding sites and AR target genes in prostate cancer cells. Here, we foc...
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/PMC5497721/ https://www.ncbi.nlm.nih.gov/pubmed/28474805 http://dx.doi.org/10.1111/cas.13269 |
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author | Ashikari, Daisaku Takayama, Ken‐ichi Obinata, Daisuke Takahashi, Satoru Inoue, Satoshi |
author_facet | Ashikari, Daisaku Takayama, Ken‐ichi Obinata, Daisuke Takahashi, Satoru Inoue, Satoshi |
author_sort | Ashikari, Daisaku |
collection | PubMed |
description | The proliferation of prostate cancer cells is controlled by the androgen receptor (AR) signaling pathway. However, the function of AR target genes has not been fully elucidated. In previous studies, we have identified global AR binding sites and AR target genes in prostate cancer cells. Here, we focused on Claudin 8 (CLDN8), a protein constituting tight junctions in cell membranes. We found one AR binding site in the promoter region and two functional androgen‐responsive elements in the sequence. Reporter assay revealed that transcriptional activation of the CLDN8 promoter by androgen is dependent on these androgen‐responsive elements. Furthermore, CLDN8 mRNA is induced by androgen time‐dependently and the induction is blocked by AR inhibitor, suggesting that AR is involved in the transcriptional activation. In addition, our functional analyses by overexpression and knockdown of CLDN8 mRNA indicate that CLDN8 promotes prostate cancer cell proliferation and migration. Claudin 8 was overexpressed in prostate cancer clinical samples compared to benign tissues. Furthermore, we found that CLDN8 regulates intracellular signal transduction and stabilizes the cytoskeleton. Taken together, these results indicate that CLDN8 functions as an AR downstream signal to facilitate the progression of prostate cancer. Claudin 8 may be a novel molecular target for prostate cancer therapy. |
format | Online Article Text |
id | pubmed-5497721 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54977212017-07-10 CLDN8, an androgen‐regulated gene, promotes prostate cancer cell proliferation and migration Ashikari, Daisaku Takayama, Ken‐ichi Obinata, Daisuke Takahashi, Satoru Inoue, Satoshi Cancer Sci Original Articles The proliferation of prostate cancer cells is controlled by the androgen receptor (AR) signaling pathway. However, the function of AR target genes has not been fully elucidated. In previous studies, we have identified global AR binding sites and AR target genes in prostate cancer cells. Here, we focused on Claudin 8 (CLDN8), a protein constituting tight junctions in cell membranes. We found one AR binding site in the promoter region and two functional androgen‐responsive elements in the sequence. Reporter assay revealed that transcriptional activation of the CLDN8 promoter by androgen is dependent on these androgen‐responsive elements. Furthermore, CLDN8 mRNA is induced by androgen time‐dependently and the induction is blocked by AR inhibitor, suggesting that AR is involved in the transcriptional activation. In addition, our functional analyses by overexpression and knockdown of CLDN8 mRNA indicate that CLDN8 promotes prostate cancer cell proliferation and migration. Claudin 8 was overexpressed in prostate cancer clinical samples compared to benign tissues. Furthermore, we found that CLDN8 regulates intracellular signal transduction and stabilizes the cytoskeleton. Taken together, these results indicate that CLDN8 functions as an AR downstream signal to facilitate the progression of prostate cancer. Claudin 8 may be a novel molecular target for prostate cancer therapy. John Wiley and Sons Inc. 2017-06-02 2017-07 /pmc/articles/PMC5497721/ /pubmed/28474805 http://dx.doi.org/10.1111/cas.13269 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‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Ashikari, Daisaku Takayama, Ken‐ichi Obinata, Daisuke Takahashi, Satoru Inoue, Satoshi CLDN8, an androgen‐regulated gene, promotes prostate cancer cell proliferation and migration |
title |
CLDN8, an androgen‐regulated gene, promotes prostate cancer cell proliferation and migration |
title_full |
CLDN8, an androgen‐regulated gene, promotes prostate cancer cell proliferation and migration |
title_fullStr |
CLDN8, an androgen‐regulated gene, promotes prostate cancer cell proliferation and migration |
title_full_unstemmed |
CLDN8, an androgen‐regulated gene, promotes prostate cancer cell proliferation and migration |
title_short |
CLDN8, an androgen‐regulated gene, promotes prostate cancer cell proliferation and migration |
title_sort | cldn8, an androgen‐regulated gene, promotes prostate cancer cell proliferation and migration |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5497721/ https://www.ncbi.nlm.nih.gov/pubmed/28474805 http://dx.doi.org/10.1111/cas.13269 |
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