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- Publisher Website: 10.1021/acs.jmedchem.4c02199
- Scopus: eid_2-s2.0-85217899323
- PMID: 39961800
- WOS: WOS:001424861200001
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Article: Opto-Epigenetic Regulation of Histone Arginine Asymmetric Dimethylation via Type I Protein Arginine Methyltransferase Inhibition
| Title | Opto-Epigenetic Regulation of Histone Arginine Asymmetric Dimethylation via Type I Protein Arginine Methyltransferase Inhibition |
|---|---|
| Authors | |
| Issue Date | 17-Feb-2025 |
| Publisher | American Chemical Society |
| Citation | Journal of Medicinal Chemistry, 2025, v. 68, n. 4, p. 4373-4381 How to Cite? |
| Abstract | Histone arginine asymmetric dimethylation, which is mainly catalyzed by type I protein arginine methyltransferases (PRMTs), is involved in broad biological and pathological processes. Recently, several type I PRMT inhibitors, such as MS023, have been developed to reverse the histone arginine dimethylation status in tumor cells, but extensive inhibition of type I PRMTs may cause side effects in normal tissues. Herein, we designed a photoactivatable MS023 prodrug (C-MS023) to achieve spatiotemporal inhibition of histone arginine asymmetric dimethylation. In vitro studies showed that C-MS023 exhibited reduced potency in inhibiting type I PRMTs. Importantly, visible light irradiation at 420 nm could trigger the photolysis of the prodrug, thereby liberating MS023 for effective downregulation of histone arginine asymmetric dimethylation and DNA replication-related transcriptomic activities. This opto-epigenetic small-molecule prodrug potentially aids in further research into the pathophysiological functions of type I PRMTs and the development of targeted epigenetic therapeutics. |
| Persistent Identifier | http://hdl.handle.net/10722/358216 |
| ISSN | 2023 Impact Factor: 6.8 2023 SCImago Journal Rankings: 1.986 |
| ISI Accession Number ID |
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Xu, Shuting | - |
| dc.contributor.author | Long, Kaiqi | - |
| dc.contributor.author | Wang, Tianyi | - |
| dc.contributor.author | Zhu, Yangyang | - |
| dc.contributor.author | Zhang, Yunjiao | - |
| dc.contributor.author | Wang, Weiping | - |
| dc.date.accessioned | 2025-07-26T00:30:24Z | - |
| dc.date.available | 2025-07-26T00:30:24Z | - |
| dc.date.issued | 2025-02-17 | - |
| dc.identifier.citation | Journal of Medicinal Chemistry, 2025, v. 68, n. 4, p. 4373-4381 | - |
| dc.identifier.issn | 0022-2623 | - |
| dc.identifier.uri | http://hdl.handle.net/10722/358216 | - |
| dc.description.abstract | Histone arginine asymmetric dimethylation, which is mainly catalyzed by type I protein arginine methyltransferases (PRMTs), is involved in broad biological and pathological processes. Recently, several type I PRMT inhibitors, such as MS023, have been developed to reverse the histone arginine dimethylation status in tumor cells, but extensive inhibition of type I PRMTs may cause side effects in normal tissues. Herein, we designed a photoactivatable MS023 prodrug (C-MS023) to achieve spatiotemporal inhibition of histone arginine asymmetric dimethylation. In vitro studies showed that C-MS023 exhibited reduced potency in inhibiting type I PRMTs. Importantly, visible light irradiation at 420 nm could trigger the photolysis of the prodrug, thereby liberating MS023 for effective downregulation of histone arginine asymmetric dimethylation and DNA replication-related transcriptomic activities. This opto-epigenetic small-molecule prodrug potentially aids in further research into the pathophysiological functions of type I PRMTs and the development of targeted epigenetic therapeutics. | - |
| dc.language | eng | - |
| dc.publisher | American Chemical Society | - |
| dc.relation.ispartof | Journal of Medicinal Chemistry | - |
| dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
| dc.title | Opto-Epigenetic Regulation of Histone Arginine Asymmetric Dimethylation via Type I Protein Arginine Methyltransferase Inhibition | - |
| dc.type | Article | - |
| dc.description.nature | published_or_final_version | - |
| dc.identifier.doi | 10.1021/acs.jmedchem.4c02199 | - |
| dc.identifier.pmid | 39961800 | - |
| dc.identifier.scopus | eid_2-s2.0-85217899323 | - |
| dc.identifier.volume | 68 | - |
| dc.identifier.issue | 4 | - |
| dc.identifier.spage | 4373 | - |
| dc.identifier.epage | 4381 | - |
| dc.identifier.eissn | 1520-4804 | - |
| dc.identifier.isi | WOS:001424861200001 | - |
| dc.identifier.issnl | 0022-2623 | - |
