Effect of ZSTK474, a Novel Phosphatidylinositol 3-Kinase Inhibitor, on DNA-Dependent Protein Kinase

被引:51
作者
Kong, Dexin [1 ]
Yaguchi, Shin-ichi [1 ,2 ]
Yamori, Takao [1 ]
机构
[1] Japanese Fdn Canc Res, Ctr Canc Chemotherapy, Div Mol Pharmacol, Koto Ku, Tokyo 1358550, Japan
[2] Zenyaku Kogyo Co Ltd, Res Lab, Nerima Ku, Tokyo 1780062, Japan
基金
日本学术振兴会;
关键词
phosphatidylinositol; 3-kinase; DNA-dependent protein kinase; ZSTK474; inhibitor; specificity; ANTITUMOR-ACTIVITY; IN-VIVO; GENE-EXPRESSION; PIK3CA GENE; CELL-LINES; PI3K-GAMMA; MUTATIONS; DATABASE; OVARIAN; TARGET;
D O I
10.1248/bpb.32.297
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Phosphatidylinositol 3-kinase (PI3K) has been implicated in a variety of diseases including cancer. A number of PI3K inhibitors have recently been developed for use in cancer therapy. ZSTK474 is a highly promising antitumor agent targeting PI3K. Ne previously reported that ZSTK474 showed potent inhibition against four class I PI3K isoforms but not against 140 protein kinases. However, whether ZSTK474 inhibits DNA-dependent protein kinase (DNA-PK), which is structurally similar to PI3K, remains unknown. To investigate the inhibition of DNA-PK, we developed a new DNA-PK assay method using Kinase-Glo. The inhibition activity of ZSTK474 against DNA-PK was determined, and shown to be far weaker compared with that observed against PI3K. The inhibition selectivity of ZSTK474 for PI3K over DNA-PK was significantly higher than other PI3K inhibitors, namely NVP-BEZ235, PI-103 and LY294002. These results indicated that ZSTK474 was the most specific agent among these PI3K inhibitors.
引用
收藏
页码:297 / 300
页数:4
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