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Characterization of aldehyde dehydrogenase isozymes in ovarian cancer tissues and sphere cultures

BACKGROUND: Aldehyde dehydrogenases belong to a superfamily of detoxifying enzymes that protect cells from carcinogenic aldehydes. Of the superfamily, ALDH1A1 has gained most attention because current studies have shown that its expression is associated with human cancer stem cells. However, ALDH1A1...

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Autores principales: Saw, Yu-Ting, Yang, Junzheng, Ng, Shu-Kay, Liu, Shubai, Singh, Surendra, Singh, Margit, Welch, William R, Tsuda, Hiroshi, Fong, Wing-Ping, Thompson, David, Vasiliou, Vasilis, Berkowitz, Ross S, Ng, Shu-Wing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458927/
https://www.ncbi.nlm.nih.gov/pubmed/22852552
http://dx.doi.org/10.1186/1471-2407-12-329
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author Saw, Yu-Ting
Yang, Junzheng
Ng, Shu-Kay
Liu, Shubai
Singh, Surendra
Singh, Margit
Welch, William R
Tsuda, Hiroshi
Fong, Wing-Ping
Thompson, David
Vasiliou, Vasilis
Berkowitz, Ross S
Ng, Shu-Wing
author_facet Saw, Yu-Ting
Yang, Junzheng
Ng, Shu-Kay
Liu, Shubai
Singh, Surendra
Singh, Margit
Welch, William R
Tsuda, Hiroshi
Fong, Wing-Ping
Thompson, David
Vasiliou, Vasilis
Berkowitz, Ross S
Ng, Shu-Wing
author_sort Saw, Yu-Ting
collection PubMed
description BACKGROUND: Aldehyde dehydrogenases belong to a superfamily of detoxifying enzymes that protect cells from carcinogenic aldehydes. Of the superfamily, ALDH1A1 has gained most attention because current studies have shown that its expression is associated with human cancer stem cells. However, ALDH1A1 is only one of the 19 human ALDH subfamilies currently known. The purpose of the present study was to determine if the expression and activities of other major ALDH isozymes are associated with human ovarian cancer and ovarian cancer sphere cultures. METHODS: Immunohistochemistry was used to delineate ALDH isozyme localization in clinical ovarian tissues. Western Blot analyses were performed on lysates prepared from cancer cell lines and ovarian cancer spheres to confirm the immunohistochemistry findings. Quantitative reverse transcription-polymerase chain reactions were used to measure the mRNA expression levels. The Aldefluor® assay was used to measure ALDH activity in cancer cells from the four tumor subtypes. RESULTS: Immunohistochemical staining showed significant overexpression of ALDH1A3, ALDH3A2, and ALDH7A1 isozymes in ovarian tumors relative to normal ovarian tissues. The expression and activity of ALDH1A1 is tumor type-dependent, as seen from immunohistochemisty, Western blot analysis, and the Aldefluor® assay. The expression was elevated in the mucinous and endometrioid ovarian epithelial tumors than in serous and clear cell tumors. In some serous and most clear cell tumors, ALDH1A1 expression was found in the stromal fibroblasts. RNA expression of all studied ALDH isozymes also showed higher expression in endometrioid and mucinous tumors than in the serous and clear cell subtypes. The expression of ALDH enzymes showed tumor type-dependent induction in ovarian cancer cells growing as sphere suspensions in serum-free medium. CONCLUSIONS: The results of our study indicate that ALDH enzyme expression and activity may be associated with specific cell types in ovarian tumor tissues and vary according to cell states. Elucidating the function of the ALDH isozymes in lineage differentiation and pathogenesis may have significant implications for ovarian cancer pathophysiology.
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spelling pubmed-34589272012-09-27 Characterization of aldehyde dehydrogenase isozymes in ovarian cancer tissues and sphere cultures Saw, Yu-Ting Yang, Junzheng Ng, Shu-Kay Liu, Shubai Singh, Surendra Singh, Margit Welch, William R Tsuda, Hiroshi Fong, Wing-Ping Thompson, David Vasiliou, Vasilis Berkowitz, Ross S Ng, Shu-Wing BMC Cancer Research Article BACKGROUND: Aldehyde dehydrogenases belong to a superfamily of detoxifying enzymes that protect cells from carcinogenic aldehydes. Of the superfamily, ALDH1A1 has gained most attention because current studies have shown that its expression is associated with human cancer stem cells. However, ALDH1A1 is only one of the 19 human ALDH subfamilies currently known. The purpose of the present study was to determine if the expression and activities of other major ALDH isozymes are associated with human ovarian cancer and ovarian cancer sphere cultures. METHODS: Immunohistochemistry was used to delineate ALDH isozyme localization in clinical ovarian tissues. Western Blot analyses were performed on lysates prepared from cancer cell lines and ovarian cancer spheres to confirm the immunohistochemistry findings. Quantitative reverse transcription-polymerase chain reactions were used to measure the mRNA expression levels. The Aldefluor® assay was used to measure ALDH activity in cancer cells from the four tumor subtypes. RESULTS: Immunohistochemical staining showed significant overexpression of ALDH1A3, ALDH3A2, and ALDH7A1 isozymes in ovarian tumors relative to normal ovarian tissues. The expression and activity of ALDH1A1 is tumor type-dependent, as seen from immunohistochemisty, Western blot analysis, and the Aldefluor® assay. The expression was elevated in the mucinous and endometrioid ovarian epithelial tumors than in serous and clear cell tumors. In some serous and most clear cell tumors, ALDH1A1 expression was found in the stromal fibroblasts. RNA expression of all studied ALDH isozymes also showed higher expression in endometrioid and mucinous tumors than in the serous and clear cell subtypes. The expression of ALDH enzymes showed tumor type-dependent induction in ovarian cancer cells growing as sphere suspensions in serum-free medium. CONCLUSIONS: The results of our study indicate that ALDH enzyme expression and activity may be associated with specific cell types in ovarian tumor tissues and vary according to cell states. Elucidating the function of the ALDH isozymes in lineage differentiation and pathogenesis may have significant implications for ovarian cancer pathophysiology. BioMed Central 2012-08-01 /pmc/articles/PMC3458927/ /pubmed/22852552 http://dx.doi.org/10.1186/1471-2407-12-329 Text en Copyright ©2012 Saw 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
Saw, Yu-Ting
Yang, Junzheng
Ng, Shu-Kay
Liu, Shubai
Singh, Surendra
Singh, Margit
Welch, William R
Tsuda, Hiroshi
Fong, Wing-Ping
Thompson, David
Vasiliou, Vasilis
Berkowitz, Ross S
Ng, Shu-Wing
Characterization of aldehyde dehydrogenase isozymes in ovarian cancer tissues and sphere cultures
title Characterization of aldehyde dehydrogenase isozymes in ovarian cancer tissues and sphere cultures
title_full Characterization of aldehyde dehydrogenase isozymes in ovarian cancer tissues and sphere cultures
title_fullStr Characterization of aldehyde dehydrogenase isozymes in ovarian cancer tissues and sphere cultures
title_full_unstemmed Characterization of aldehyde dehydrogenase isozymes in ovarian cancer tissues and sphere cultures
title_short Characterization of aldehyde dehydrogenase isozymes in ovarian cancer tissues and sphere cultures
title_sort characterization of aldehyde dehydrogenase isozymes in ovarian cancer tissues and sphere cultures
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458927/
https://www.ncbi.nlm.nih.gov/pubmed/22852552
http://dx.doi.org/10.1186/1471-2407-12-329
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