地高辛及其对心血管疾病和癌症的 Na+/K+-ATP 酶靶向作用

IF 3.3 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Yulin Ren, Andrew T. Anderson, Gunnar Meyer, Kaitlyn M. Lauber, Judith C. Gallucci, A. Douglas Kinghorn
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引用次数: 0

摘要

Na+/K+-ATP 酶(NKA)是一种质膜离子转运蛋白,参与产生和维持跨细胞膜的 Na+ 和 K+ 梯度,从而为代谢底物的二次转运提供动力。NKA 还能调节细胞内的钙离子,而钙离子负责调节许多细胞过程,同时它还能与许多其他蛋白质相互作用,发挥信号转导功能,其中涉及多种信号通路。因此,NKA 已成为治疗人类疾病的重要靶点。强心苷是著名的 NKA 抑制剂,其中 (+)- 地高辛或地高辛长期以来一直被用于治疗充血性心力衰竭。此外,地高辛还通过直接靶向 HIF-1α、NKA 和 NF-κB 而显示出潜在的抗肿瘤活性。因此,本综述总结了 NKA 在人类心血管疾病和癌症中的功能以及地高辛对这些疾病的治疗作用,并讨论了地高辛、NKA、心血管疾病和癌症之间的相关性。本综述还介绍了地高辛的单糖强心苷类似物的抗肿瘤潜力,包括(-)-隐丹参苷 A、(-)-高良姜苷、(-)-ouabain 和 (+)-strebloside 。希望这篇论文能为设计和发现治疗心血管疾病和癌症的新型强心甙类治疗药物提供一些有用的信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Digoxin and its Na+/K+-ATPase-targeted actions on cardiovascular diseases and cancer

Digoxin and its Na+/K+-ATPase-targeted actions on cardiovascular diseases and cancer
Na+/K+-ATPase (NKA) is a plasma membrane ion-transporting protein involved in the generation and maintenance of Na+ and K+ gradients across the cell membrane, which can produce a driving force for the secondary transport of metabolic substrates. NKA also regulates intracellular calcium that is responsible for modulating numerous cellular processes, while it interacts with many other proteins and functions as a signal transducer, with several signaling pathways being involved. Thus, NKA has become an important target for the treatment of human diseases. Cardiac glycosides are well-known NKA inhibitors, of which (+)-digoxin or digoxin has been long used for the treatment of congestive heart failure. Also, digoxin has exhibited potential antitumor activity, by targeting directly HIF-1α, NKA, and NF-κB. Thus, the function of NKA in human cardiovascular diseases and cancer and the therapeutic effects of digoxin on these diseases are summarized in the present review, with the correlations among digoxin, NKA, cardiovascular diseases, and cancer being discussed. Presented herein are also the antitumor potential of monosaccharide cardiac glycoside analogues of digoxin, including (−)-cryptanoside A, (−)-oleandrin, (−)-ouabain, and (+)-strebloside. It is hoped that this contribution will provide some helpful information for the design and discovery of new cardiac glycoside-type therapeutic agents for the treatment of cardiovascular diseases and cancer.
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来源期刊
Bioorganic & Medicinal Chemistry
Bioorganic & Medicinal Chemistry 医学-生化与分子生物学
CiteScore
6.80
自引率
2.90%
发文量
413
审稿时长
17 days
期刊介绍: Bioorganic & Medicinal Chemistry provides an international forum for the publication of full original research papers and critical reviews on molecular interactions in key biological targets such as receptors, channels, enzymes, nucleotides, lipids and saccharides. The aim of the journal is to promote a better understanding at the molecular level of life processes, and living organisms, as well as the interaction of these with chemical agents. A special feature will be that colour illustrations will be reproduced at no charge to the author, provided that the Editor agrees that colour is essential to the information content of the illustration in question.
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