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Anti-apoptotic effect of claudin-1 in tamoxifen-treated human breast cancer MCF-7 cells
BACKGROUND: Claudin-1 is a membrane protein of tight junctions, and is associated with the development of various cancers. However, the significance of claudin-1 expression in cancer cells is not well understood. Here, we showed for the first time the anti-apoptotic effect of claudin-1 in human brea...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2958956/ https://www.ncbi.nlm.nih.gov/pubmed/20937153 http://dx.doi.org/10.1186/1471-2407-10-548 |
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author | Akasaka, Harue Sato, Fuyuki Morohashi, Satoko Wu, Yunyan Liu, Yang Kondo, Jun Odagiri, Hiroki Hakamada, Kenichi Kijima, Hiroshi |
author_facet | Akasaka, Harue Sato, Fuyuki Morohashi, Satoko Wu, Yunyan Liu, Yang Kondo, Jun Odagiri, Hiroki Hakamada, Kenichi Kijima, Hiroshi |
author_sort | Akasaka, Harue |
collection | PubMed |
description | BACKGROUND: Claudin-1 is a membrane protein of tight junctions, and is associated with the development of various cancers. However, the significance of claudin-1 expression in cancer cells is not well understood. Here, we showed for the first time the anti-apoptotic effect of claudin-1 in human breast cancer MCF-7 cells. METHODS: Human breast cancer MCF-7 and T47 D cells were treated with or without tamoxifen, siRNA against claudin-1, or tamoxifen and claudin-1 siRNA. The samples were analyzed by RT-PCR, Western blotting or immunofluorescent staining. RESULTS: The expression of claudin-1 was upregulated in tamoxifen-treated MCF-7 cells, whereas the expression of claudin-1 was not altered in tamoxifen-treated T47 D cells. Knockdown of claudin-1 by siRNA increased the amount of poly (ADP-ribose) polymerase (PARP) regardless of tamoxifen treatment in MCF-7 cells, but not T47 D cells. In the cell membranes of the MCF-7 cells, tamoxifen treatment increased the amount of claudin-1, but decreased the amount of β-catenin. Claudin-1 siRNA increased the amount of E-cadherin in the cytoplasm of the MCF-7 cells as well as the amount of β-catenin in their cell membranes. CONCLUSION: These results indicate that claudin-1 has anti-apoptotic effects, and is involved in the regulation of the expression and subcellular localization of β-catenin and E-cadherin in MCF-7, but not T47 D cells. |
format | Text |
id | pubmed-2958956 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29589562010-10-22 Anti-apoptotic effect of claudin-1 in tamoxifen-treated human breast cancer MCF-7 cells Akasaka, Harue Sato, Fuyuki Morohashi, Satoko Wu, Yunyan Liu, Yang Kondo, Jun Odagiri, Hiroki Hakamada, Kenichi Kijima, Hiroshi BMC Cancer Research Article BACKGROUND: Claudin-1 is a membrane protein of tight junctions, and is associated with the development of various cancers. However, the significance of claudin-1 expression in cancer cells is not well understood. Here, we showed for the first time the anti-apoptotic effect of claudin-1 in human breast cancer MCF-7 cells. METHODS: Human breast cancer MCF-7 and T47 D cells were treated with or without tamoxifen, siRNA against claudin-1, or tamoxifen and claudin-1 siRNA. The samples were analyzed by RT-PCR, Western blotting or immunofluorescent staining. RESULTS: The expression of claudin-1 was upregulated in tamoxifen-treated MCF-7 cells, whereas the expression of claudin-1 was not altered in tamoxifen-treated T47 D cells. Knockdown of claudin-1 by siRNA increased the amount of poly (ADP-ribose) polymerase (PARP) regardless of tamoxifen treatment in MCF-7 cells, but not T47 D cells. In the cell membranes of the MCF-7 cells, tamoxifen treatment increased the amount of claudin-1, but decreased the amount of β-catenin. Claudin-1 siRNA increased the amount of E-cadherin in the cytoplasm of the MCF-7 cells as well as the amount of β-catenin in their cell membranes. CONCLUSION: These results indicate that claudin-1 has anti-apoptotic effects, and is involved in the regulation of the expression and subcellular localization of β-catenin and E-cadherin in MCF-7, but not T47 D cells. BioMed Central 2010-10-12 /pmc/articles/PMC2958956/ /pubmed/20937153 http://dx.doi.org/10.1186/1471-2407-10-548 Text en Copyright ©2010 Akasaka et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Akasaka, Harue Sato, Fuyuki Morohashi, Satoko Wu, Yunyan Liu, Yang Kondo, Jun Odagiri, Hiroki Hakamada, Kenichi Kijima, Hiroshi Anti-apoptotic effect of claudin-1 in tamoxifen-treated human breast cancer MCF-7 cells |
title | Anti-apoptotic effect of claudin-1 in tamoxifen-treated human breast cancer MCF-7 cells |
title_full | Anti-apoptotic effect of claudin-1 in tamoxifen-treated human breast cancer MCF-7 cells |
title_fullStr | Anti-apoptotic effect of claudin-1 in tamoxifen-treated human breast cancer MCF-7 cells |
title_full_unstemmed | Anti-apoptotic effect of claudin-1 in tamoxifen-treated human breast cancer MCF-7 cells |
title_short | Anti-apoptotic effect of claudin-1 in tamoxifen-treated human breast cancer MCF-7 cells |
title_sort | anti-apoptotic effect of claudin-1 in tamoxifen-treated human breast cancer mcf-7 cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2958956/ https://www.ncbi.nlm.nih.gov/pubmed/20937153 http://dx.doi.org/10.1186/1471-2407-10-548 |
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