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Aldehyde dehydrogenase 1 expression is correlated with poor prognosis in breast cancer
Breast cancer (BC) is one of the most common cancers worldwide, and is a major cause of death in women. Aldehyde dehydrogenase 1 (ALDH1) is a marker of stem cells and cancer stem cells, and its activity correlates with the outcome of various tumors, including BC. This study aimed to analyze the rela...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5484203/ https://www.ncbi.nlm.nih.gov/pubmed/28640095 http://dx.doi.org/10.1097/MD.0000000000007171 |
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author | Yao, Juan Jin, Qin Wang, Xu-dong Zhu, Hui-jun Ni, Qi-chao |
author_facet | Yao, Juan Jin, Qin Wang, Xu-dong Zhu, Hui-jun Ni, Qi-chao |
author_sort | Yao, Juan |
collection | PubMed |
description | Breast cancer (BC) is one of the most common cancers worldwide, and is a major cause of death in women. Aldehyde dehydrogenase 1 (ALDH1) is a marker of stem cells and cancer stem cells, and its activity correlates with the outcome of various tumors, including BC. This study aimed to analyze the relationship between ALDH1 expression and clinicopathological characters in BC and the prognostic significance of ALDH1. We used quantitative reverse-transcription PCR (qRT-PCR) to detect ALDHA1 mRNA levels in 25 fresh frozen BC samples and matched noncancerous samples. Immunohistochemistry on tissue microarrays was used to analyze protein expression in 137 paraffin-embedded BC tissues and corresponding noncancerous tissues. STATA 16.0 software was used for statistical analysis. The results suggested that levels of both ALDH1 mRNA and protein in BC were significantly higher than in corresponding adjacent breast samples (3.856 ± 0.3442 vs 1.385 ± 0.1534, P < .001; 52.6% vs 25.5%, P < .001, respectively). ALDH1 protein expression was also significantly associated with histological grade (P = .017), tumor size (P = .017), and tumor–node–metastasis (TNM) stage (P = .038). Multivariate analysis using the Cox regression model demonstrated that ALDH1 expression (P = .024), molecular typing (P = .046), and TNM classification (P = .034) were independent predictive factors for the outcome of BC. Kaplan–Meier analysis and the log-rank test indicated that patients with high ALDH1 expression, triple-negative BC, and advanced TNM stage had a reduced overall survival time. These data suggest that ALDH1 could be used as a prognostic factor for BC and may provide a useful therapeutic target in the treatment of BC. |
format | Online Article Text |
id | pubmed-5484203 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-54842032017-07-06 Aldehyde dehydrogenase 1 expression is correlated with poor prognosis in breast cancer Yao, Juan Jin, Qin Wang, Xu-dong Zhu, Hui-jun Ni, Qi-chao Medicine (Baltimore) 5750 Breast cancer (BC) is one of the most common cancers worldwide, and is a major cause of death in women. Aldehyde dehydrogenase 1 (ALDH1) is a marker of stem cells and cancer stem cells, and its activity correlates with the outcome of various tumors, including BC. This study aimed to analyze the relationship between ALDH1 expression and clinicopathological characters in BC and the prognostic significance of ALDH1. We used quantitative reverse-transcription PCR (qRT-PCR) to detect ALDHA1 mRNA levels in 25 fresh frozen BC samples and matched noncancerous samples. Immunohistochemistry on tissue microarrays was used to analyze protein expression in 137 paraffin-embedded BC tissues and corresponding noncancerous tissues. STATA 16.0 software was used for statistical analysis. The results suggested that levels of both ALDH1 mRNA and protein in BC were significantly higher than in corresponding adjacent breast samples (3.856 ± 0.3442 vs 1.385 ± 0.1534, P < .001; 52.6% vs 25.5%, P < .001, respectively). ALDH1 protein expression was also significantly associated with histological grade (P = .017), tumor size (P = .017), and tumor–node–metastasis (TNM) stage (P = .038). Multivariate analysis using the Cox regression model demonstrated that ALDH1 expression (P = .024), molecular typing (P = .046), and TNM classification (P = .034) were independent predictive factors for the outcome of BC. Kaplan–Meier analysis and the log-rank test indicated that patients with high ALDH1 expression, triple-negative BC, and advanced TNM stage had a reduced overall survival time. These data suggest that ALDH1 could be used as a prognostic factor for BC and may provide a useful therapeutic target in the treatment of BC. Wolters Kluwer Health 2017-06-23 /pmc/articles/PMC5484203/ /pubmed/28640095 http://dx.doi.org/10.1097/MD.0000000000007171 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | 5750 Yao, Juan Jin, Qin Wang, Xu-dong Zhu, Hui-jun Ni, Qi-chao Aldehyde dehydrogenase 1 expression is correlated with poor prognosis in breast cancer |
title | Aldehyde dehydrogenase 1 expression is correlated with poor prognosis in breast cancer |
title_full | Aldehyde dehydrogenase 1 expression is correlated with poor prognosis in breast cancer |
title_fullStr | Aldehyde dehydrogenase 1 expression is correlated with poor prognosis in breast cancer |
title_full_unstemmed | Aldehyde dehydrogenase 1 expression is correlated with poor prognosis in breast cancer |
title_short | Aldehyde dehydrogenase 1 expression is correlated with poor prognosis in breast cancer |
title_sort | aldehyde dehydrogenase 1 expression is correlated with poor prognosis in breast cancer |
topic | 5750 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5484203/ https://www.ncbi.nlm.nih.gov/pubmed/28640095 http://dx.doi.org/10.1097/MD.0000000000007171 |
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