Powis G, Phil D
Arizona Cancer Center, University of Arizona Health Sciences Center, Tucson 85724.
Cancer Metastasis Rev. 1994 Mar;13(1):91-103. doi: 10.1007/BF00690420.
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.
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。