TY - JOUR
T1 - 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
AU - Anraku, Tsutomu
AU - Kuroki, Hiroo
AU - Kazama, Akira
AU - Bilim, Vladimir
AU - Tasaki, Masaaki
AU - Schmitt, Daniel
AU - Mazar, Andrew
AU - Giles, Francis J.
AU - Ugolkov, Andrey
AU - Tomita, Yoshihiko
N1 - Publisher Copyright:
© 2020 Spandidos Publications. All rights reserved.
PY - 2020
Y1 - 2020
N2 - 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-3α and GSK-3β, and GSK-3β 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-3β 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.
AB - 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-3α and GSK-3β, and GSK-3β 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-3β 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.
KW - Apoptosis
KW - Cell cycle arrest
KW - Glycogen synthase kinase-3
KW - Immune cells
KW - Renal cell carcinoma
UR - http://www.scopus.com/inward/record.url?scp=85077765984&partnerID=8YFLogxK
U2 - 10.3892/ijmm.2019.4427
DO - 10.3892/ijmm.2019.4427
M3 - Article
C2 - 31894292
AN - SCOPUS:85077765984
SN - 1107-3756
VL - 45
SP - 315
EP - 323
JO - International Journal of Molecular Medicine
JF - International Journal of Molecular Medicine
IS - 2
ER -