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

被引:4
|
作者
Furuya, Kai [1 ]
Fujibayashi, So [1 ]
Wu, Tao [1 ]
Takahashi, Kouhei [1 ]
Takase, Shin [1 ]
Orimoto, Ai [1 ]
Sugano, Eriko [1 ]
Tomita, Hiroshi [1 ]
Kashiwagi, Sayo [2 ]
Kiyono, Tohru [3 ]
Ishii, Tsuyoshi [2 ]
Fukuda, Tomokazu [1 ]
机构
[1] Iwate Univ, Grad Sch Sci & Engn, 4-3-5 Ueda, Morioka, Iwate 0208551, Japan
[2] Rohto Pharmaceut Co Ltd, Basic Res Dev Div, 6-5-4 Kunimidai, Kizugawa, Kyoto 6190216, Japan
[3] Natl Canc Ctr, Exploratory Oncol Res & Clin Trial Ctr, 6-5-1 Kashiwanoha, Kashiwa, Chiba 2778577, Japan
来源
BMC GENOMIC DATA | 2022年 / 23卷 / 01期
关键词
Androgen receptor; Dermal papilla cells; RNA-Seq; CAVEOLIN-1;
D O I
10.1186/s12863-021-01018-6
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background 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. Results 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. Conclusion Our whole transcriptome data is critical resources for discovery of new therapeutic targets for testosterone-related diseases.
引用
收藏
页数:10
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