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用 N-丙炔基甘氨酸对 HYPDH/PRODH2 进行治疗靶向治疗为高草酸尿症治疗提供了机会。

Therapeutic targeting of HYPDH/PRODH2 with N-propargylglycine offers a Hyperoxaluria treatment opportunity.

机构信息

Buck Institute for Research on Aging, Novato, CA, USA.

Departments of Biochemistry and Chemistry, University of Missouri, Columbia, MO, USA.

出版信息

Biochim Biophys Acta Mol Basis Dis. 2024 Jan;1870(1):166848. doi: 10.1016/j.bbadis.2023.166848. Epub 2023 Aug 14.

Abstract

N-propargylglycine prevents 4-hydroxyproline catabolism in mouse liver and kidney. N-propargylglycine is a novel suicide inhibitor of PRODH2 and induces mitochondrial degradation of PRODH2. PRODH2 is selectively expressed in liver and kidney and contributes to primary hyperoxaluria (PH). Preclinical evaluation of N-propargylglycine efficacy as a new PH therapeutic is warranted.

摘要

N-丙炔基甘氨酸可防止小鼠肝、肾中 4-羟脯氨酸的分解代谢。N-丙炔基甘氨酸是 PRODH2 的新型自杀抑制剂,并诱导 PRODH2 的线粒体降解。PRODH2 选择性地在肝和肾中表达,并有助于原发性高草酸尿症(PH)。需要对 N-丙炔基甘氨酸作为新型 PH 治疗药物的疗效进行临床前评估。

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4
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J Pers Med. 2021 Jan 27;11(2):74. doi: 10.3390/jpm11020074.
5
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Acta Biochim Biophys Sin (Shanghai). 2020 Dec 11;52(11):1181-1190. doi: 10.1093/abbs/gmaa113.
6
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7
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8
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J Am Soc Nephrol. 2018 Jun;29(6):1615-1623. doi: 10.1681/ASN.2017040390. Epub 2018 Mar 27.

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