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| Main Authors: | , , , , , , , , , , |
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| Format: | Artículo científico |
| Language: | en |
| Published: |
Journal of medicinal chemistry
2025
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| Subjects: | |
| Online Access: | https://pubmed.ncbi.nlm.nih.gov/41001936/ |
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| _version_ | 1868266149463982081 |
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| author | Feng, Di Fan, Xinli Hu, Yuqiang Man, Yizhi Wang, Qian Song, Yanmin Zhou, Jingjing Zhang, Jin Luo, Yun Wang, Jing Tang, Xinjing |
| author_facet | Feng, Di Fan, Xinli Hu, Yuqiang Man, Yizhi Wang, Qian Song, Yanmin Zhou, Jingjing Zhang, Jin Luo, Yun Wang, Jing Tang, Xinjing Feng, Di Fan, Xinli Hu, Yuqiang Man, Yizhi Wang, Qian Song, Yanmin Zhou, Jingjing Zhang, Jin Luo, Yun Wang, Jing Tang, Xinjing |
| collection | PubMed - marine biology |
| contents | Efficient Silencing of Androgen Receptor Gene via UTR-Targeting siRNAs for Androgenetic Alopecia Therapy. Feng, Di Fan, Xinli Hu, Yuqiang Man, Yizhi Wang, Qian Song, Yanmin Zhou, Jingjing Zhang, Jin Luo, Yun Wang, Jing Tang, Xinjing Alopecia Receptors, Androgen Animals RNA, Small Interfering Humans Mice Male Gene Silencing Dihydrotestosterone Mice, Inbred C57BL Androgenetic alopecia (AGA) is predominantly driven by excessive local activity of dihydrotestosterone (DHT), leading to follicular miniaturization and progressive hair loss. The need for novel treatment strategies for AGA is emphasized by the side effects and postoperative sequelae of current therapeutic approaches, including pharmacological interventions and surgical procedures. Small-interfering RNAs (siRNAs) have emerged as promising therapeutic candidates due to their target specificity, the enhanced efficacy, and long-term effect. Here, we screened a series of siRNA sequences targeting non-coding region of androgen receptor (AR) gene and identified a lead siRNA candidate (AR-27) conserved between and. The chemically modified and cholesterol-conjugated candidate (AR-27 E-Chol) was evaluated in both cells and DHT-induced AGA mice model. AR-27 E-Chol effectively stimulated dorsal hair regrowth and significantly downregulated AR gene expression in skin tissues. These findings support the clinical potential of AR-27 E-Chol as an effective therapeutic candidate for AGA. |
| format | Artículo científico |
| id | pubmed_41001936 |
| institution | PubMed |
| language | en |
| publishDate | 2025 |
| publisher | Journal of medicinal chemistry |
| record_format | pubmed |
| spellingShingle | Efficient Silencing of Androgen Receptor Gene via UTR-Targeting siRNAs for Androgenetic Alopecia Therapy. Feng, Di Fan, Xinli Hu, Yuqiang Man, Yizhi Wang, Qian Song, Yanmin Zhou, Jingjing Zhang, Jin Luo, Yun Wang, Jing Tang, Xinjing Alopecia Receptors, Androgen Animals RNA, Small Interfering Humans Mice Male Gene Silencing Dihydrotestosterone Mice, Inbred C57BL Efficient Silencing of Androgen Receptor Gene via UTR-Targeting siRNAs for Androgenetic Alopecia Therapy. Feng, Di Fan, Xinli Hu, Yuqiang Man, Yizhi Wang, Qian Song, Yanmin Zhou, Jingjing Zhang, Jin Luo, Yun Wang, Jing Tang, Xinjing Alopecia Receptors, Androgen Animals RNA, Small Interfering Humans Mice Male Gene Silencing Dihydrotestosterone Mice, Inbred C57BL Androgenetic alopecia (AGA) is predominantly driven by excessive local activity of dihydrotestosterone (DHT), leading to follicular miniaturization and progressive hair loss. The need for novel treatment strategies for AGA is emphasized by the side effects and postoperative sequelae of current therapeutic approaches, including pharmacological interventions and surgical procedures. Small-interfering RNAs (siRNAs) have emerged as promising therapeutic candidates due to their target specificity, the enhanced efficacy, and long-term effect. Here, we screened a series of siRNA sequences targeting non-coding region of androgen receptor (AR) gene and identified a lead siRNA candidate (AR-27) conserved between and. The chemically modified and cholesterol-conjugated candidate (AR-27 E-Chol) was evaluated in both cells and DHT-induced AGA mice model. AR-27 E-Chol effectively stimulated dorsal hair regrowth and significantly downregulated AR gene expression in skin tissues. These findings support the clinical potential of AR-27 E-Chol as an effective therapeutic candidate for AGA. |
| title | Efficient Silencing of Androgen Receptor Gene via UTR-Targeting siRNAs for Androgenetic Alopecia Therapy. |
| topic | Alopecia Receptors, Androgen Animals RNA, Small Interfering Humans Mice Male Gene Silencing Dihydrotestosterone Mice, Inbred C57BL |
| url | https://pubmed.ncbi.nlm.nih.gov/41001936/ |