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Article: Opto-Epigenetic Regulation of Histone Arginine Asymmetric Dimethylation via Type I Protein Arginine Methyltransferase Inhibition

TitleOpto-Epigenetic Regulation of Histone Arginine Asymmetric Dimethylation via Type I Protein Arginine Methyltransferase Inhibition
Authors
Issue Date17-Feb-2025
PublisherAmerican Chemical Society
Citation
Journal of Medicinal Chemistry, 2025, v. 68, n. 4, p. 4373-4381 How to Cite?
AbstractHistone 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 Identifierhttp://hdl.handle.net/10722/358216
ISSN
2023 Impact Factor: 6.8
2023 SCImago Journal Rankings: 1.986
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorXu, Shuting-
dc.contributor.authorLong, Kaiqi-
dc.contributor.authorWang, Tianyi-
dc.contributor.authorZhu, Yangyang-
dc.contributor.authorZhang, Yunjiao-
dc.contributor.authorWang, Weiping-
dc.date.accessioned2025-07-26T00:30:24Z-
dc.date.available2025-07-26T00:30:24Z-
dc.date.issued2025-02-17-
dc.identifier.citationJournal of Medicinal Chemistry, 2025, v. 68, n. 4, p. 4373-4381-
dc.identifier.issn0022-2623-
dc.identifier.urihttp://hdl.handle.net/10722/358216-
dc.description.abstractHistone 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.languageeng-
dc.publisherAmerican Chemical Society-
dc.relation.ispartofJournal of Medicinal Chemistry-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleOpto-Epigenetic Regulation of Histone Arginine Asymmetric Dimethylation via Type I Protein Arginine Methyltransferase Inhibition -
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1021/acs.jmedchem.4c02199-
dc.identifier.pmid39961800-
dc.identifier.scopuseid_2-s2.0-85217899323-
dc.identifier.volume68-
dc.identifier.issue4-
dc.identifier.spage4373-
dc.identifier.epage4381-
dc.identifier.eissn1520-4804-
dc.identifier.isiWOS:001424861200001-
dc.identifier.issnl0022-2623-

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