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

  • Tsutomu Anraku
  • , Hiroo Kuroki
  • , Akira Kazama
  • , Vladimir Bilim
  • , Masaaki Tasaki
  • , Daniel Schmitt
  • , Andrew Mazar
  • , Francis J. Giles
  • , Andrey Ugolkov
  • , Yoshihiko Tomita

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

20 Citations (Scopus)

Abstract

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.

Original languageEnglish
Pages (from-to)315-323
Number of pages9
JournalInternational Journal of Molecular Medicine
Volume45
Issue number2
DOIs
Publication statusPublished - 2020
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Apoptosis
  • Cell cycle arrest
  • Glycogen synthase kinase-3
  • Immune cells
  • Renal cell carcinoma

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