Suppr超能文献

磷脂酰肌醇信号传导抑制剂作为抗增殖剂。

Inhibitors of phosphatidylinositol signalling as antiproliferative agents.

作者信息

Powis G, Phil D

机构信息

Arizona Cancer Center, University of Arizona Health Sciences Center, Tucson 85724.

出版信息

Cancer Metastasis Rev. 1994 Mar;13(1):91-103. doi: 10.1007/BF00690420.

Abstract

Intracellular signalling pathways mediating the effects of oncogenes on cell growth and transformation offer novel targets for the development of anticancer drugs. With this approach it may be sufficient to target a component of the signalling pathway activated by the oncogene rather than the oncogene product itself. Phosphatidylinositol (PtdIns) is a key component of two growth factor signalling pathways. It acts as a substrate for PtdIns specific phospholipase C (PtdInsPLC) and for PtdIns-3-kinase. In this review the antiproliferative properties of some inhibitors of PtdInsPLC and PtdIns-3-kinase are considered. There are some compounds already in clinical trial as anticancer drugs that may act by inhibiting PtdIns signalling, as well as several compounds in preclinical development. Some problems that may be encountered in developing this new class of anticancer drugs are discussed.

摘要

介导癌基因对细胞生长和转化作用的细胞内信号传导途径为抗癌药物的研发提供了新的靶点。通过这种方法,靶向癌基因激活的信号传导途径的一个组成部分可能就足够了,而不必靶向癌基因产物本身。磷脂酰肌醇(PtdIns)是两条生长因子信号传导途径的关键组成部分。它作为磷脂酰肌醇特异性磷脂酶C(PtdInsPLC)和磷脂酰肌醇-3-激酶的底物。在这篇综述中,我们考虑了一些磷脂酰肌醇磷脂酶C和磷脂酰肌醇-3-激酶抑制剂的抗增殖特性。已经有一些作为抗癌药物正在进行临床试验的化合物可能通过抑制磷脂酰肌醇信号传导起作用,还有几种化合物正处于临床前开发阶段。本文讨论了开发这类新型抗癌药物可能遇到的一些问题。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验