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Transcriptome analysis and prognosis of ALDH isoforms in human cancer

Overexpression of ALDH is associated with cancer stem-like features and poor cancer prognosis. High ALDH activity has been observed in cancer stem-like cells. There are a total of 19 human ALDH isoforms, all of which are associated with reducing oxidative stress and protecting cells from damage. How...

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Autores principales: Chang, Peter Mu-Hsin, Chen, Che-Hong, Yeh, Chi-Chun, Lu, Hsueh-Ju, Liu, Tze-Tze, Chen, Ming-Huang, Liu, Chun-Yu, Wu, Alexander T. H., Yang, Muh-Hwa, Tai, Shyh-Kuan, Mochly-Rosen, Daria, Huang, Chi-Ying F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5807355/
https://www.ncbi.nlm.nih.gov/pubmed/29426835
http://dx.doi.org/10.1038/s41598-018-21123-4
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author Chang, Peter Mu-Hsin
Chen, Che-Hong
Yeh, Chi-Chun
Lu, Hsueh-Ju
Liu, Tze-Tze
Chen, Ming-Huang
Liu, Chun-Yu
Wu, Alexander T. H.
Yang, Muh-Hwa
Tai, Shyh-Kuan
Mochly-Rosen, Daria
Huang, Chi-Ying F.
author_facet Chang, Peter Mu-Hsin
Chen, Che-Hong
Yeh, Chi-Chun
Lu, Hsueh-Ju
Liu, Tze-Tze
Chen, Ming-Huang
Liu, Chun-Yu
Wu, Alexander T. H.
Yang, Muh-Hwa
Tai, Shyh-Kuan
Mochly-Rosen, Daria
Huang, Chi-Ying F.
author_sort Chang, Peter Mu-Hsin
collection PubMed
description Overexpression of ALDH is associated with cancer stem-like features and poor cancer prognosis. High ALDH activity has been observed in cancer stem-like cells. There are a total of 19 human ALDH isoforms, all of which are associated with reducing oxidative stress and protecting cells from damage. However, it is unknown whether all ALDHs are associated with poor cancer prognosis and which ones play a significant role in cancer progression. In this study, we used RNA sequencing data from The Cancer Genome Atlas (TCGA) to evaluate the differential expression of 19 ALDH isoforms in 5 common human cancers. The 19 ALDH genes were analyzed with an integrating meta-analysis of cancer prognosis. Genotyping and next-generation RNA sequencing for 30 pairwise samples of head and neck squamous cell carcinoma were performed and compared with the TCGA cohort. The analysis showed that each ALDH isoform had a specific differential expression pattern, most of which were related to prognosis in human cancer. A lower expression of ALDH2 in the tumor was observed, which was independent from the ALDH2 rs671 SNP variant and the expression of other mitochondria-associated protein coding genes. This study provides new insight into the association between ALDH expression and cancer prognosis.
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spelling pubmed-58073552018-02-14 Transcriptome analysis and prognosis of ALDH isoforms in human cancer Chang, Peter Mu-Hsin Chen, Che-Hong Yeh, Chi-Chun Lu, Hsueh-Ju Liu, Tze-Tze Chen, Ming-Huang Liu, Chun-Yu Wu, Alexander T. H. Yang, Muh-Hwa Tai, Shyh-Kuan Mochly-Rosen, Daria Huang, Chi-Ying F. Sci Rep Article Overexpression of ALDH is associated with cancer stem-like features and poor cancer prognosis. High ALDH activity has been observed in cancer stem-like cells. There are a total of 19 human ALDH isoforms, all of which are associated with reducing oxidative stress and protecting cells from damage. However, it is unknown whether all ALDHs are associated with poor cancer prognosis and which ones play a significant role in cancer progression. In this study, we used RNA sequencing data from The Cancer Genome Atlas (TCGA) to evaluate the differential expression of 19 ALDH isoforms in 5 common human cancers. The 19 ALDH genes were analyzed with an integrating meta-analysis of cancer prognosis. Genotyping and next-generation RNA sequencing for 30 pairwise samples of head and neck squamous cell carcinoma were performed and compared with the TCGA cohort. The analysis showed that each ALDH isoform had a specific differential expression pattern, most of which were related to prognosis in human cancer. A lower expression of ALDH2 in the tumor was observed, which was independent from the ALDH2 rs671 SNP variant and the expression of other mitochondria-associated protein coding genes. This study provides new insight into the association between ALDH expression and cancer prognosis. Nature Publishing Group UK 2018-02-09 /pmc/articles/PMC5807355/ /pubmed/29426835 http://dx.doi.org/10.1038/s41598-018-21123-4 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chang, Peter Mu-Hsin
Chen, Che-Hong
Yeh, Chi-Chun
Lu, Hsueh-Ju
Liu, Tze-Tze
Chen, Ming-Huang
Liu, Chun-Yu
Wu, Alexander T. H.
Yang, Muh-Hwa
Tai, Shyh-Kuan
Mochly-Rosen, Daria
Huang, Chi-Ying F.
Transcriptome analysis and prognosis of ALDH isoforms in human cancer
title Transcriptome analysis and prognosis of ALDH isoforms in human cancer
title_full Transcriptome analysis and prognosis of ALDH isoforms in human cancer
title_fullStr Transcriptome analysis and prognosis of ALDH isoforms in human cancer
title_full_unstemmed Transcriptome analysis and prognosis of ALDH isoforms in human cancer
title_short Transcriptome analysis and prognosis of ALDH isoforms in human cancer
title_sort transcriptome analysis and prognosis of aldh isoforms in human cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5807355/
https://www.ncbi.nlm.nih.gov/pubmed/29426835
http://dx.doi.org/10.1038/s41598-018-21123-4
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