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Glycogen Synthase Kinase 3β in Cancer Biology and Treatment
Takahiro Domoto1, Masahiro Uehara1, Dilireba Bolidong1
1Division of Translational and Clinical Oncology, Cancer Research Institute, Kanazawa University, Kanazawa 920-0934, Japan.
Abstract:
Glycogen synthase kinase (GSK)3β is a multifunctional serine/threonine protein kinase with more than 100 substrates and interacting molecules. GSK3β is normally active in cells and negative regulation of GSK3β activity via phosphorylation of its serine 9 residue is required for most normal cells to maintain homeostasis. Aberrant expression and activity of GSK3β contributes to the pathogenesis and progression of common recalcitrant diseases such as glucose intolerance, neurodegenerative disorders and cancer. Despite recognized roles against several proto-oncoproteins and mediators of the epithelial-mesenchymal transition, deregulated GSK3β also participates in tumor cell survival, evasion of apoptosis, proliferation and invasion, as well as sustaining cancer stemness and inducing therapy resistance. A therapeutic effect from GSK3β inhibition has been demonstrated in 25 different cancer types. Moreover, there is increasing evidence that GSK3β inhibition protects normal cells and tissues from the harmful effects associated with conventional cancer therapies. Here, we review the evidence supporting aberrant GSK3β as a hallmark property of cancer and highlight the beneficial effects of GSK3β inhibition on normal cells and tissues during cancer therapy. The biological rationale for targeting GSK3β in the treatment of cancer is also discussed at length.
Insights
Glycogen synthase kinase (GSK)3β, a key regulator, is implicated in cancer development and progression. Inhibiting GSK3β shows therapeutic promise in various cancers and protects normal cells during cancer therapy.
Area of Science:
- Biochemistry
- Molecular Biology
- Oncology
Background:
- Glycogen synthase kinase (GSK)3β is a serine/threonine kinase regulating numerous cellular processes.
- GSK3β hyperactivity is linked to diseases like diabetes, neurodegeneration, and cancer.
- Normal cellular homeostasis requires GSK3β activity regulation via phosphorylation.
Purpose of the Study:
- To review evidence linking aberrant GSK3β to cancer.
- To highlight the protective effects of GSK3β inhibition on normal tissues during cancer treatment.
- To discuss the rationale for targeting GSK3β in cancer therapy.
Main Methods:
- Literature review of studies on GSK3β in cancer.
- Analysis of data on GSK3β inhibition in preclinical and clinical cancer models.
- Examination of GSK3β's role in normal cell protection during oncological therapies.
Main Results:
- Aberrant GSK3β is a hallmark of 25 cancer types, contributing to tumor survival, invasion, and therapy resistance.
- GSK3β inhibition demonstrates therapeutic effects across diverse cancers.
- GSK3β inhibition protects normal cells and tissues from conventional cancer therapy side effects.
Conclusions:
- Targeting GSK3β is a promising therapeutic strategy for cancer treatment.
- GSK3β inhibition offers a dual benefit: direct anti-cancer effects and protection of normal tissues.
- Further research into GSK3β inhibitors is warranted for comprehensive cancer care.
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