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中性鞘磷脂酶作为药物设计的靶点。

Neutral sphingomyelinase as a target for drug design.

作者信息

Wascholowski V, Giannis A

机构信息

Department of Organic Chemistry, Institute of Organic Chemistry, University of Karlsruhe, Karlsruhe, Germany.

出版信息

Drug News Perspect. 2001 Dec;14(10):581-90.

Abstract

The sphingolipid ceramide is an important second messenger assumed to be involved in fundamental processes, including proliferation, differentiation and growth arrest, as well as the induction of apoptosis. Ceramide is generated in a ubiquitous and evolutionarily conserved signaling pathway called the sphingomyelin pathway, through the action of distinct isoforms of sphingomyelinases. An improved understanding of sphingomyelinase-dependent signaling may offer significant insights into the regulation of physiological and pathological processes and may finally provide novel strategies and new targets for pharmacological intervention (e.g., in inflammatory responses, neurodegenerative diseases and cancer). This article summarizes the current knowledge of the role of neutral sphingomyelinase (N-SMase) in cell signaling pathways, and its potential meaning, and demonstrates the opportunity of a specific inhibition of N-SMases as a novel therapeutic target.

摘要

鞘脂神经酰胺是一种重要的第二信使,被认为参与包括增殖、分化、生长停滞以及细胞凋亡诱导等基本过程。神经酰胺通过鞘磷脂酶不同亚型的作用,在一种普遍存在且进化保守的信号通路即鞘磷脂通路中产生。对鞘磷脂酶依赖性信号传导的深入理解可能为生理和病理过程的调控提供重要见解,并最终为药物干预(如在炎症反应、神经退行性疾病和癌症中)提供新的策略和靶点。本文总结了目前关于中性鞘磷脂酶(N-SMase)在细胞信号通路中的作用及其潜在意义的知识,并阐述了将N-SMases作为新型治疗靶点进行特异性抑制的可能性。

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