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Comprehensive transcriptome data to identify downstream genes of testosterone signalling in dermal papilla cells
Testosterone-related steroid hormones are associated with various types of diseases, including prostate cancer and androgenetic alopecia (AGA). The testosterone or dihydroxy testosterone (DHT) circulates through the blood, binds to the androgen receptor (AR) in the cytoplasm, and finally enters the...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9709033/ https://www.ncbi.nlm.nih.gov/pubmed/36446804 http://dx.doi.org/10.1038/s41597-022-01846-w |
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author | Matsusaka, Himari Wu, Tao Furuya, Kai Yamada-Kato, Tomoe Bai, Lanlan Tomita, Hiroshi Sugano, Eriko Ozaki, Taku Kiyono, Tohru Okunishi, Isao Fukuda, Tomokazu |
author_facet | Matsusaka, Himari Wu, Tao Furuya, Kai Yamada-Kato, Tomoe Bai, Lanlan Tomita, Hiroshi Sugano, Eriko Ozaki, Taku Kiyono, Tohru Okunishi, Isao Fukuda, Tomokazu |
author_sort | Matsusaka, Himari |
collection | PubMed |
description | Testosterone-related steroid hormones are associated with various types of diseases, including prostate cancer and androgenetic alopecia (AGA). The testosterone or dihydroxy testosterone (DHT) circulates through the blood, binds to the androgen receptor (AR) in the cytoplasm, and finally enters the nucleus to activate downstream target genes. We previously found that immortalized dermal papilla cells (DPCs) lost AR expression, which may be explained by the repeated cell passages of DPCs. To compensate for the AR expression, DPCs that express AR exogenously were established. In this study, we performed an RNA-Seq analysis of the AR-expressing and non-AR-expressing DPCs in the presence or absence of DHT to identify the downstream target genes regulated by AR signalling. Furthermore, we treated DPCs with minoxidil sulphate, which has the potential to treat AGA. This is the first comprehensive analysis to identify the downstream genes involved in testosterone signalling in DPCs. Our manuscript provides high-priority data for the discovery of molecular targets for prostate cancer and AGA. |
format | Online Article Text |
id | pubmed-9709033 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97090332022-12-01 Comprehensive transcriptome data to identify downstream genes of testosterone signalling in dermal papilla cells Matsusaka, Himari Wu, Tao Furuya, Kai Yamada-Kato, Tomoe Bai, Lanlan Tomita, Hiroshi Sugano, Eriko Ozaki, Taku Kiyono, Tohru Okunishi, Isao Fukuda, Tomokazu Sci Data Data Descriptor Testosterone-related steroid hormones are associated with various types of diseases, including prostate cancer and androgenetic alopecia (AGA). The testosterone or dihydroxy testosterone (DHT) circulates through the blood, binds to the androgen receptor (AR) in the cytoplasm, and finally enters the nucleus to activate downstream target genes. We previously found that immortalized dermal papilla cells (DPCs) lost AR expression, which may be explained by the repeated cell passages of DPCs. To compensate for the AR expression, DPCs that express AR exogenously were established. In this study, we performed an RNA-Seq analysis of the AR-expressing and non-AR-expressing DPCs in the presence or absence of DHT to identify the downstream target genes regulated by AR signalling. Furthermore, we treated DPCs with minoxidil sulphate, which has the potential to treat AGA. This is the first comprehensive analysis to identify the downstream genes involved in testosterone signalling in DPCs. Our manuscript provides high-priority data for the discovery of molecular targets for prostate cancer and AGA. Nature Publishing Group UK 2022-11-29 /pmc/articles/PMC9709033/ /pubmed/36446804 http://dx.doi.org/10.1038/s41597-022-01846-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Data Descriptor Matsusaka, Himari Wu, Tao Furuya, Kai Yamada-Kato, Tomoe Bai, Lanlan Tomita, Hiroshi Sugano, Eriko Ozaki, Taku Kiyono, Tohru Okunishi, Isao Fukuda, Tomokazu Comprehensive transcriptome data to identify downstream genes of testosterone signalling in dermal papilla cells |
title | Comprehensive transcriptome data to identify downstream genes of testosterone signalling in dermal papilla cells |
title_full | Comprehensive transcriptome data to identify downstream genes of testosterone signalling in dermal papilla cells |
title_fullStr | Comprehensive transcriptome data to identify downstream genes of testosterone signalling in dermal papilla cells |
title_full_unstemmed | Comprehensive transcriptome data to identify downstream genes of testosterone signalling in dermal papilla cells |
title_short | Comprehensive transcriptome data to identify downstream genes of testosterone signalling in dermal papilla cells |
title_sort | comprehensive transcriptome data to identify downstream genes of testosterone signalling in dermal papilla cells |
topic | Data Descriptor |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9709033/ https://www.ncbi.nlm.nih.gov/pubmed/36446804 http://dx.doi.org/10.1038/s41597-022-01846-w |
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