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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...

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Autores principales: Akasaka, Harue, Sato, Fuyuki, Morohashi, Satoko, Wu, Yunyan, Liu, Yang, Kondo, Jun, Odagiri, Hiroki, Hakamada, Kenichi, Kijima, Hiroshi
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
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.
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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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