Hill S R, Bonjouklian R, Powis G, Abraham R T, Ashendel C L, Zalkow L H
Arizona Cancer Center, University of Arizona, Tucson 85724.
Anticancer Drug Des. 1994 Aug;9(4):353-61.
A convenient and reliable multisample assay for the screening of inhibitors of the growth factor signalling enzyme phosphatidylinositol specific phospholipase C (PtdInsPLC) has been developed. Three naturally occurring peptide inhibitors of PtdInsPLC have been identified, myroridin K, streptothricin B and edeine, with IC50 values of 8.3, 6.7 and 16.1 microM, respectively. All three peptides inhibited colony formation of HT-29 human colon adenocarcinoma cells, with IC50 values of 7.2, 3.9 and 13.0 microM, respectively. The compounds also inhibited the growth of other human cancer cells in culture. One of the peptides, myroridin K, has previously been reported to have in vivo antitumour activity. It is possible that inhibition of PtdInsPLC is responsible for the cell growth inhibition and antitumour properties of the peptide compounds.
已开发出一种便捷可靠的多样本检测方法,用于筛选生长因子信号酶磷脂酰肌醇特异性磷脂酶C(PtdInsPLC)的抑制剂。已鉴定出三种天然存在的PtdInsPLC肽抑制剂,即肉珊瑚素K、链丝菌素B和伊短菌素,其IC50值分别为8.3、6.7和16.1微摩尔。这三种肽均抑制HT-29人结肠腺癌细胞的集落形成,IC50值分别为7.2、3.9和13.0微摩尔。这些化合物还抑制培养中的其他人类癌细胞生长。其中一种肽,肉珊瑚素K,此前已报道具有体内抗肿瘤活性。肽类化合物对细胞生长的抑制作用和抗肿瘤特性可能是由于对PtdInsPLC的抑制。