Transcriptome analysis to identify the downstream genes of androgen receptor in dermal papilla cells

Testosterone signaling mediates various diseases, such as androgenetic alopecia and prostate cancer. Testosterone signaling is mediated by the androgen receptor (AR). In this study, we fortuitously found that primary and immortalized dermal papilla cells suppressed AR expression, although dermal pap...

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Veröffentlicht in:BMC genetics 2022-01, Vol.23 (1), p.2-2, Article 2
Hauptverfasser: Furuya, Kai, Fujibayashi, So, Wu, Tao, Takahashi, Kouhei, Takase, Shin, Orimoto, Ai, Sugano, Eriko, Tomita, Hiroshi, Kashiwagi, Sayo, Kiyono, Tohru, Ishii, Tsuyoshi, Fukuda, Tomokazu
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Sprache:eng
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Zusammenfassung:Testosterone signaling mediates various diseases, such as androgenetic alopecia and prostate cancer. Testosterone signaling is mediated by the androgen receptor (AR). In this study, we fortuitously found that primary and immortalized dermal papilla cells suppressed AR expression, although dermal papilla cells express AR in vivo. To analyze the AR signaling pathway, we exogenously introduced the AR gene via a retrovirus into immortalized dermal papilla cells and comprehensively compared their expression profiles with and without AR expression. Whole-transcriptome profiling revealed that the focal adhesion pathway was mainly affected by the activation of AR signaling. In particular, we found that caveolin-1 gene expression was downregulated in AR-expressing cells, suggesting that caveolin-1 is controlled by AR. Our whole transcriptome data is critical resources for discovery of new therapeutic targets for testosterone-related diseases.
ISSN:2730-6844
2730-6844
1471-2156
DOI:10.1186/s12863-021-01018-6