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O’Halloran, Thomas V.

https://orcid.org/0000-0001-8732-5059

Mayo Clinic

Northwestern University

Citations 1

Molecular Pathways: Revisiting Glycogen Synthase Kinase-3β as a Target for the Treatment of Cancer
Walz, Amy L. , Ugolkov, Andrey , Chandra, Sunandana , Kozikowski, Alan P. , Carneiro, Benedito A. , O’Halloran, Thomas V. , Billadeau, Daniel D. , Mazar, Andrew P. , Giles, Francis Joseph

Clinical Cancer Research | January 5, 2017 | Volume: 23 | Issue: 8 | Pages: 1891-1897

10.1158/1078-0432.ccr-15-2240 Get It

Abstract Glycogen synthase kinase-3β (GSK-3β), a serine/threonine protein kinase, is a complex regulator of numerous cellular functions. GSK-3β is a unique kinase which is constitutively active in resting and nonstimulated cells. GSK-3β has been implicated in a wide range of diseases including neurodegeneration, inflammation and fibrosis, noninsulin-dependent diabetes mellitus, and cancer. It is a regulator of NF-κB–mediated survival of cancer cells, which provided a rationale for the development of GSK-3 inhibitors targeting malignant tumors. Recent studies, many of them reported over the past decade, have identified GSK-3β as a potential therapeutic target in more than 15 different types of cancer. Whereas only active GSK-3β is expressed in cancer cell nucleus, aberrant nuclear accumulation of GSK-3β has been identified as a hallmark of cancer cells in malignant tumors of different origin. This review focuses on the preclinical and clinical development of GSK-3 inhibitors and the potential therapeutic impact of targeting GSK-3β in human cancer. Clin Cancer Res; 23(8); 1891–7. ©2017 AACR.