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      The role of glycogen synthase kinase 3 (GSK3) in cancer with emphasis on ovarian cancer development and progression: A comprehensive review

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          Abstract

          Glycogen synthase kinase 3 (GSK3) is a monomeric serine-threonine kinase discovered in 1980 in a rat skeletal muscle. It has been involved in various cellular processes including embryogenesis, immune response, inflammation, apoptosis, autophagy, wound healing, neurodegeneration, and carcinogenesis. GSK3 exists in two different isoforms, GSK3α and GSK3β, both containing seven antiparallel beta-plates, a short linking part and an alpha helix, but coded by different genes and variously expressed in human tissues. In the current review, we comprehensively appraise the current literature on the role of GSK3 in various cancers with emphasis on ovarian carcinoma. Our findings indicate that the role of GSK3 in ovarian cancer development cannot be decisively determined as the currently available data support both prooncogenic and tumor-suppressive effects. Likewise, the clinical impact of GSK3 expression on ovarian cancer patients and its potential therapeutic implications are also limited. Further studies are needed to fully elucidate the pathophysiological and clinical implications of GSK3 activity in ovarian cancer.

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          Most cited references140

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          The renaissance of GSK3.

          Glycogen synthase kinase 3 (GSK3) was initially described as a key enzyme involved in glycogen metabolism, but is now known to regulate a diverse array of cell functions. The study of the substrate specificity and regulation of GSK3 activity has been important in the quest for therapeutic intervention.
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            Glycogen synthase kinase-3 (GSK3): regulation, actions, and diseases.

            Glycogen synthase kinase-3 (GSK3) may be the busiest kinase in most cells, with over 100 known substrates to deal with. How does GSK3 maintain control to selectively phosphorylate each substrate, and why was it evolutionarily favorable for GSK3 to assume such a large responsibility? GSK3 must be particularly adaptable for incorporating new substrates into its repertoire, and we discuss the distinct properties of GSK3 that may contribute to its capacity to fulfill its roles in multiple signaling pathways. The mechanisms regulating GSK3 (predominantly post-translational modifications, substrate priming, cellular trafficking, protein complexes) have been reviewed previously, so here we focus on newly identified complexities in these mechanisms, how each of these regulatory mechanism contributes to the ability of GSK3 to select which substrates to phosphorylate, and how these mechanisms may have contributed to its adaptability as new substrates evolved. The current understanding of the mechanisms regulating GSK3 is reviewed, as are emerging topics in the actions of GSK3, particularly its interactions with receptors and receptor-coupled signal transduction events, and differential actions and regulation of the two GSK3 isoforms, GSK3α and GSK3β. Another remarkable characteristic of GSK3 is its involvement in many prevalent disorders, including psychiatric and neurological diseases, inflammatory diseases, cancer, and others. We address the feasibility of targeting GSK3 therapeutically, and provide an update of its involvement in the etiology and treatment of several disorders.
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              AKT as a Therapeutic Target for Cancer

              Many cellular processes in cancer are attributed to kinase signaling networks. V-akt murine thymoma viral oncogene homolog (AKT) plays a major role in the PI3K/AKT signaling pathways. AKT is activated by PI3K or phosphoinositide-dependent kinases (PDK) as well as growth factors, inflammation, and DNA damage. Signal transduction occurs through downstream effectors such as mTOR, glycogen synthase kinase 3 beta (GSK3β), or forkhead box protein O1 (FOXO1). The abnormal overexpression or activation of AKT has been observed in many cancers, including ovarian, lung, and pancreatic cancers, and is associated with increased cancer cell proliferation and survival. Therefore, targeting AKT could provide an important approach for cancer prevention and therapy. In this review, we discuss the rationale for targeting AKT and also provide details regarding synthetic and natural AKT-targeting compounds and their associated studies.
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                Author and article information

                Journal
                Bosn J Basic Med Sci
                Bosn J Basic Med Sci
                Bosnian Journal of Basic Medical Sciences
                Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina (Bosnia )
                1512-8601
                1840-4812
                February 2021
                : 21
                : 1
                : 5-18
                Affiliations
                [1 ]Department of Biology, School of Medicine, University of Zagreb, Zagreb, Croatia
                [2 ]Centre of Excellence in Reproductive and Regenerative Medicine, University of Zagreb School of Medicine, Zagreb, Croatia
                [3 ]Department of Obstetrics and Gynecology, School of Medicine, University of Zagreb, Zagreb, Croatia
                [4 ]Clinic of Obstetrics and Gynecology, Clinical Hospital “Sveti Duh”, Zagreb, Croatia
                [5 ]College of Medicine, QU Health, Qatar University, Doha, Qatar
                Author notes
                [* ] Corresponding author: Alan Serman, MD PhD, Clinic of Obstetrics and Gynecology, Clinical Hospital “Sveti Duh”, Sveti Duh 64, 10000 Zagreb, Croatia. E-mail: sermana@ 123456mef.hr
                Article
                BJBMS-21-5
                10.17305/bjbms.2020.5036
                7861620
                32767962
                6f1f6fdd-8b52-4ab1-8d95-e011d00a5b36
                Copyright: © The Author(s) (2021)

                This work is licensed under a Creative Commons Attribution 4.0 International License

                History
                : 01 August 2020
                : 04 August 2020
                Categories
                Review Article

                gsk3,ovarian cancer,therapeutic target
                gsk3, ovarian cancer, therapeutic target

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