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Localization of hRad9 in breast cancer

BACKGROUND: hRad9 is a cell cycle checkpoint gene that is up-regulated in breast cancer. We have previously shown that the mRNA up-regulation correlated with tumor size and local recurrence. Immunohistochemical studies were made to better define the role of hRad9 in breast carcinogenesis. METHODS: L...

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Autores principales: Chan, Vivian, Khoo, US, Wong, MS, Lau, Ken, Suen, Dacita, Li, George, Kwong, Ava, Chan, TK
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2483722/
https://www.ncbi.nlm.nih.gov/pubmed/18616832
http://dx.doi.org/10.1186/1471-2407-8-196
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author Chan, Vivian
Khoo, US
Wong, MS
Lau, Ken
Suen, Dacita
Li, George
Kwong, Ava
Chan, TK
author_facet Chan, Vivian
Khoo, US
Wong, MS
Lau, Ken
Suen, Dacita
Li, George
Kwong, Ava
Chan, TK
author_sort Chan, Vivian
collection PubMed
description BACKGROUND: hRad9 is a cell cycle checkpoint gene that is up-regulated in breast cancer. We have previously shown that the mRNA up-regulation correlated with tumor size and local recurrence. Immunohistochemical studies were made to better define the role of hRad9 in breast carcinogenesis. METHODS: Localisation of hRad9 protein were performed on paired tumor and normal breast tissues. Immunoblotting with and without dephosphorylation was used to define the protein isolated from breast cancer cells. RESULTS: Increased hRad9 protein was observed in breast cancer cells nucleus compared to non-tumor epithelium. This nuclear protein existed in hyperphosphorylated forms which may be those of the hRad9-hRad1-hHus1 complex. CONCLUSION: Finding of hyperphosphorylated forms of hRad9 in the nucleus of cancer cells is in keeping with its function in ameliorating DNA instability, whereby it inadvertently assists tumor growth.
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spelling pubmed-24837222008-07-25 Localization of hRad9 in breast cancer Chan, Vivian Khoo, US Wong, MS Lau, Ken Suen, Dacita Li, George Kwong, Ava Chan, TK BMC Cancer Research Article BACKGROUND: hRad9 is a cell cycle checkpoint gene that is up-regulated in breast cancer. We have previously shown that the mRNA up-regulation correlated with tumor size and local recurrence. Immunohistochemical studies were made to better define the role of hRad9 in breast carcinogenesis. METHODS: Localisation of hRad9 protein were performed on paired tumor and normal breast tissues. Immunoblotting with and without dephosphorylation was used to define the protein isolated from breast cancer cells. RESULTS: Increased hRad9 protein was observed in breast cancer cells nucleus compared to non-tumor epithelium. This nuclear protein existed in hyperphosphorylated forms which may be those of the hRad9-hRad1-hHus1 complex. CONCLUSION: Finding of hyperphosphorylated forms of hRad9 in the nucleus of cancer cells is in keeping with its function in ameliorating DNA instability, whereby it inadvertently assists tumor growth. BioMed Central 2008-07-11 /pmc/articles/PMC2483722/ /pubmed/18616832 http://dx.doi.org/10.1186/1471-2407-8-196 Text en Copyright © 2008 Chan 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
Chan, Vivian
Khoo, US
Wong, MS
Lau, Ken
Suen, Dacita
Li, George
Kwong, Ava
Chan, TK
Localization of hRad9 in breast cancer
title Localization of hRad9 in breast cancer
title_full Localization of hRad9 in breast cancer
title_fullStr Localization of hRad9 in breast cancer
title_full_unstemmed Localization of hRad9 in breast cancer
title_short Localization of hRad9 in breast cancer
title_sort localization of hrad9 in breast cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2483722/
https://www.ncbi.nlm.nih.gov/pubmed/18616832
http://dx.doi.org/10.1186/1471-2407-8-196
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