Ciraolo Elisa, Perino Alessia, Hirsch Emilio
Department of Genetics, Biology and Biochemistry, Molecular Biotechnology Center, University of Torino, Torino, Italy.
Methods Mol Biol. 2012;795:55-67. doi: 10.1007/978-1-61779-337-0_4.
Class IA phosphoinositide-3 kinases (PI3Ks) signaling has recently emerged as a key element in cancer development because of its ability to trigger a complex panoply of cellular responses controlling survival and proliferation. Many cancers show inappropriately activated PI3K pathway, and tumors with high PI3K activity are frequently resistant to traditional chemotherapy. Indeed, preclinical studies demonstrated a prominent role for the PI3K pathway in cancer cell survival and growth, thus validating PI3K as a potential drug target in cancer. The emerging interest in inhibiting PI3Ks in cancer have prompted the aggressive development of new selective PI3K pathway inhibitors as cancer therapy, and many of these molecules are currently in early-phase clinical trials. In this chapter, we describe methods to measure the PI3K lipid kinase activity in vitro, which is the standard procedure to test the efficacy of inhibitors.
IA类磷酸肌醇-3激酶(PI3Ks)信号传导最近已成为癌症发展中的关键因素,因为它能够引发一系列复杂的细胞反应,从而控制细胞存活和增殖。许多癌症显示PI3K通路被异常激活,PI3K活性高的肿瘤通常对传统化疗耐药。事实上,临床前研究表明PI3K通路在癌细胞存活和生长中起重要作用,从而验证了PI3K作为癌症潜在药物靶点的地位。对癌症中抑制PI3Ks的兴趣日益浓厚,促使人们积极开发新的选择性PI3K通路抑制剂作为癌症治疗药物,其中许多分子目前正处于早期临床试验阶段。在本章中,我们描述了体外测量PI3K脂质激酶活性的方法,这是测试抑制剂疗效的标准程序。