Clinically relevant GSK-3β inhibitor 9-ING-41 is active as a single agent and in combination with other antitumor therapies in human renal cancer

被引:18
作者
Anraku, Tsutomu [1 ]
Kuroki, Hiroo [1 ]
Kazama, Akira [1 ]
Bilim, Vladimir [1 ,2 ]
Tasaki, Masaaki [1 ]
Schmitt, Daniel [3 ]
Mazar, Andrew [4 ]
Giles, Francis J. [3 ]
Ugolkov, Andrey [3 ]
Tomita, Yoshihiko [1 ]
机构
[1] Niigata Univ, Grad Sch Med & Dent Sci, Div Mol Oncol, Dept Urol, Niigata 9518510, Japan
[2] Kameda Daiichi Hosp, Dept Urol, Niigata 9500165, Japan
[3] Actuate Therapeut, Ft Worth, TX 76107 USA
[4] Monopar Therapeut, Wilmette, IL 60091 USA
关键词
glycogen synthase kinase-3; renal cell carcinoma; apoptosis; cell cycle arrest; immune cells; GLYCOGEN-SYNTHASE KINASE-3; FACTOR-KAPPA-B; 3-BETA INHIBITORS; TARGET; SUNITINIB; PAZOPANIB; APOPTOSIS; AUTOPHAGY; SURVIVAL; CELLS;
D O I
10.3892/ijmm.2019.4427
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Glycogen synthase kinase-3 (GSK-3), a serine/threonine kinase, is involved in a broad range of pathological processes including cancer. GSK-3 has two isoforms, GSK-3 alpha and GSK-3 beta, and GSK-3 beta has been recognized as a therapeutic target for the development of new anticancer drugs. The present study aimed to investigate the antitumor effects of 9-ING-41, which is a maleimide-based ATP-competitive small molecule GSK-3 beta inhibitor active in patients with advanced cancer. In renal cancer cell lines, treatment with 9-ING-41 alone induced cell cycle arrest and apoptosis, and autophagy inhibitors increased the antitumor effects of 9-ING-41 when used in combination. Treatment with 9-ING-41 potentiated the antitumor effects of targeted therapeutics and increased the cytotoxic effects of cytokine-activated immune cells on renal cancer cell lines. These results provided a compelling rationale for the inclusion of patients with renal cancer in studies of 9-ING-41, both as a single agent and in combination with current standard therapies.
引用
收藏
页码:315 / 323
页数:9
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