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Review article

Molecular Pathways: Revisiting Glycogen Synthase Kinase-3β as a Target for the Treatment of Cancer

Amy L. Walz1Department of Hematology/Oncology, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IllinoisAndrey Ugolkov2Developmental Therapeutic Program, Division of Hematology/Oncology, Feinberg School of Medicine, Northwestern University, Chicago, IllinoisSunandana Chandra2Developmental Therapeutic Program, Division of Hematology/Oncology, Feinberg School of Medicine, Northwestern University, Chicago, IllinoisAlan P. Kozikowski5Department of Medicinal Chemistry and Pharmacognosy, University of Illinois at Chicago, Chicago, IllinoisBenedito A. Carneiro2Developmental Therapeutic Program, Division of Hematology/Oncology, Feinberg School of Medicine, Northwestern University, Chicago, IllinoisThomas V. O’Halloran3Chemistry of Life Processes Institute, Northwestern University, Evanston, IllinoisFrancis J. Giles2Developmental Therapeutic Program, Division of Hematology/Oncology, Feinberg School of Medicine, Northwestern University, Chicago, IllinoisDaniel D. Billadeau6Division of Oncology Research, Schulze Center for Novel Therapeutics, College of Medicine, Mayo Clinic, Rochester, MinnesotaAndrew P. Mazar3Chemistry of Life Processes Institute, Northwestern University, Evanston, Illinois
2017en
ABI

Abstract

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.

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