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      Glutamate and its receptors in cancer

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          Abstract

          Glutamate, a nonessential amino acid, is a major bioenergetic substrate for proliferating normal and neoplastic cells on one hand and an excitatory neurotransmitter that is actively involved in biosynthetic, bioenergetic, metabolic, and oncogenic signaling pathways on the other. It exerts its action through a family of receptors consisting of metabotropic glutamate receptors (mGluRs) and ionotropic glutamate receptors (iGluRs), both of which have been implicated previously in a broad spectrum of acute and chronic neurodegenerative diseases. In this review, we discuss existing data on the role of glutamate as a growth factor for neoplastic cells, the expression of glutamate receptors in various types of benign and malignant neoplasms, and the potential roles that GluRs play in cancer development and progression along with their clinical significance. We conclude that glutamate-related receptors and their signaling pathways may provide novel therapeutic opportunities for a variety of malignant human diseases.

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          Most cited references102

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          Cloned glutamate receptors.

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            Diverse somatic mutation patterns and pathway alterations in human cancers.

            The systematic characterization of somatic mutations in cancer genomes is essential for understanding the disease and for developing targeted therapeutics. Here we report the identification of 2,576 somatic mutations across approximately 1,800 megabases of DNA representing 1,507 coding genes from 441 tumours comprising breast, lung, ovarian and prostate cancer types and subtypes. We found that mutation rates and the sets of mutated genes varied substantially across tumour types and subtypes. Statistical analysis identified 77 significantly mutated genes including protein kinases, G-protein-coupled receptors such as GRM8, BAI3, AGTRL1 (also called APLNR) and LPHN3, and other druggable targets. Integrated analysis of somatic mutations and copy number alterations identified another 35 significantly altered genes including GNAS, indicating an expanded role for galpha subunits in multiple cancer types. Furthermore, our experimental analyses demonstrate the functional roles of mutant GNAO1 (a Galpha subunit) and mutant MAP2K4 (a member of the JNK signalling pathway) in oncogenesis. Our study provides an overview of the mutational spectra across major human cancers and identifies several potential therapeutic targets.
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              NMDA receptor subunits: diversity, development and disease

              Current Opinion in Neurobiology, 11(3), 327-335
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                Author and article information

                Contributors
                +48-81-7423794 , +48-81-7423793 , andrzej.stepulak@gmail.com , andrzej.stepulak@umlub.pl
                Journal
                J Neural Transm
                J Neural Transm
                Journal of Neural Transmission
                Springer Vienna (Vienna )
                0300-9564
                1435-1463
                9 March 2014
                9 March 2014
                2014
                : 121
                : 933-944
                Affiliations
                [ ]Department of Biochemistry and Molecular Biology, Medical University in Lublin, ul. Chodzki 1, 20-093 Lublin, Poland
                [ ]Department of Otolaryngology, MSW Hospital, Lublin, Poland
                [ ]Department of Neurological Surgery, Medical University of Lublin, Lublin, Poland
                [ ]Department of Physiopathology, Institute of Agricultural Medicine, Lublin, Poland
                [ ]Section of Child Neurology, Department of Neurology, University of Wisconsin Madison, Madison, USA
                Article
                1182
                10.1007/s00702-014-1182-6
                4133641
                24610491
                04be7b32-c4ab-4bbf-b25f-2f3039c11b7b
                © The Author(s) 2014

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.

                History
                : 15 December 2013
                : 19 February 2014
                Categories
                Translational Neurosciences - Review article
                Custom metadata
                © Springer-Verlag Wien 2014

                Neurosciences
                glutamate receptor,cancer,growth factor,prognosis
                Neurosciences
                glutamate receptor, cancer, growth factor, prognosis

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