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Identification of cancer-type specific expression patterns for active aldehyde dehydrogenase (ALDH) isoforms in ALDEFLUOR assay

Aldehyde dehydrogenases (ALDHs) defend intracellular homeostasis by catalyzing the conversion of toxic aldehydes into non-toxic carboxylic acids, which is of particular importance to the self-renewal of stem cells and cancer stem cells. The widely used ALDEFLUOR assay was initially designed to indic...

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Autores principales: Zhou, Lei, Sheng, Dandan, Wang, Dong, Ma, Wei, Deng, Qiaodan, Deng, Lu, Liu, Suling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6424948/
https://www.ncbi.nlm.nih.gov/pubmed/30220009
http://dx.doi.org/10.1007/s10565-018-9444-y
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author Zhou, Lei
Sheng, Dandan
Wang, Dong
Ma, Wei
Deng, Qiaodan
Deng, Lu
Liu, Suling
author_facet Zhou, Lei
Sheng, Dandan
Wang, Dong
Ma, Wei
Deng, Qiaodan
Deng, Lu
Liu, Suling
author_sort Zhou, Lei
collection PubMed
description Aldehyde dehydrogenases (ALDHs) defend intracellular homeostasis by catalyzing the conversion of toxic aldehydes into non-toxic carboxylic acids, which is of particular importance to the self-renewal of stem cells and cancer stem cells. The widely used ALDEFLUOR assay was initially designed to indicate the activity of ALDH1A1 in leukemia and has been demonstrated to detect the enzyme activity of several other ALDH isoforms in various cancer types in recent years. However, it is still elusive which isoforms, among the 19 ALDH isoforms in human genome, are the potential contributors in catalyzing ALDEFLUOR assay in different cancers. In the current study, we performed a screening via overexpressing each ALDH isoform to assess their ability of catalyzing ALDEFLUOR assay. Our results demonstrate that nine isoforms are active in ALDEFLUOR assay, whose overexpression significantly increases ALDH-positive (ALDH(+)) population. Further analysis of the expression of these active isoforms in various cancers reveals cancer-type specific expression patterns, suggesting that different cancer types may exhibit ALDEFLUOR activity through expression of specific active ALDH isoforms. This study strongly indicates that a detailed elucidation of the functions for each active ALDH isoform in CSCs is necessary and important for a profound understanding of the underlying mechanisms of ALDH-associated stemness. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10565-018-9444-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-64249482019-04-05 Identification of cancer-type specific expression patterns for active aldehyde dehydrogenase (ALDH) isoforms in ALDEFLUOR assay Zhou, Lei Sheng, Dandan Wang, Dong Ma, Wei Deng, Qiaodan Deng, Lu Liu, Suling Cell Biol Toxicol Short Communication Aldehyde dehydrogenases (ALDHs) defend intracellular homeostasis by catalyzing the conversion of toxic aldehydes into non-toxic carboxylic acids, which is of particular importance to the self-renewal of stem cells and cancer stem cells. The widely used ALDEFLUOR assay was initially designed to indicate the activity of ALDH1A1 in leukemia and has been demonstrated to detect the enzyme activity of several other ALDH isoforms in various cancer types in recent years. However, it is still elusive which isoforms, among the 19 ALDH isoforms in human genome, are the potential contributors in catalyzing ALDEFLUOR assay in different cancers. In the current study, we performed a screening via overexpressing each ALDH isoform to assess their ability of catalyzing ALDEFLUOR assay. Our results demonstrate that nine isoforms are active in ALDEFLUOR assay, whose overexpression significantly increases ALDH-positive (ALDH(+)) population. Further analysis of the expression of these active isoforms in various cancers reveals cancer-type specific expression patterns, suggesting that different cancer types may exhibit ALDEFLUOR activity through expression of specific active ALDH isoforms. This study strongly indicates that a detailed elucidation of the functions for each active ALDH isoform in CSCs is necessary and important for a profound understanding of the underlying mechanisms of ALDH-associated stemness. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10565-018-9444-y) contains supplementary material, which is available to authorized users. Springer Netherlands 2018-09-15 2019 /pmc/articles/PMC6424948/ /pubmed/30220009 http://dx.doi.org/10.1007/s10565-018-9444-y Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Short Communication
Zhou, Lei
Sheng, Dandan
Wang, Dong
Ma, Wei
Deng, Qiaodan
Deng, Lu
Liu, Suling
Identification of cancer-type specific expression patterns for active aldehyde dehydrogenase (ALDH) isoforms in ALDEFLUOR assay
title Identification of cancer-type specific expression patterns for active aldehyde dehydrogenase (ALDH) isoforms in ALDEFLUOR assay
title_full Identification of cancer-type specific expression patterns for active aldehyde dehydrogenase (ALDH) isoforms in ALDEFLUOR assay
title_fullStr Identification of cancer-type specific expression patterns for active aldehyde dehydrogenase (ALDH) isoforms in ALDEFLUOR assay
title_full_unstemmed Identification of cancer-type specific expression patterns for active aldehyde dehydrogenase (ALDH) isoforms in ALDEFLUOR assay
title_short Identification of cancer-type specific expression patterns for active aldehyde dehydrogenase (ALDH) isoforms in ALDEFLUOR assay
title_sort identification of cancer-type specific expression patterns for active aldehyde dehydrogenase (aldh) isoforms in aldefluor assay
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6424948/
https://www.ncbi.nlm.nih.gov/pubmed/30220009
http://dx.doi.org/10.1007/s10565-018-9444-y
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