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      SOCE and cancer: Recent progress and new perspectives

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          Abstract

          Ca 2+ acts as a universal and versatile second messenger in the regulation of a myriad of biological processes, including cell proliferation, differentiation, migration and apoptosis. Store‐operated Ca 2+ entry (SOCE) mediated by ORAI and the stromal interaction molecule (STIM) constitutes one of the major routes of calcium entry in nonexcitable cells, in which the depletion of intracellular Ca 2+ stores triggers activation of the endoplasmic reticulum (ER)‐resident Ca 2+ sensor protein STIM to gate and open the ORAI Ca 2+ channels in the plasma membrane (PM). Accumulating evidence indicates that SOCE plays critical roles in cancer cell proliferation, metastasis and tumor neovascularization, as well as in antitumor immunity. We summarize herein the recent advances in our understanding of the function of SOCE in various types of tumor cells, vascular endothelial cells and cells of the immune system. Finally, the therapeutic potential of SOCE inhibitors in the treatment of cancer is also discussed.

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          Most cited references138

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            TRP channels.

            The TRP (Transient Receptor Potential) superfamily of cation channels is remarkable in that it displays greater diversity in activation mechanisms and selectivities than any other group of ion channels. The domain organizations of some TRP proteins are also unusual, as they consist of linked channel and enzyme domains. A unifying theme in this group is that TRP proteins play critical roles in sensory physiology, which include contributions to vision, taste, olfaction, hearing, touch, and thermo- and osmosensation. In addition, TRP channels enable individual cells to sense changes in their local environment. Many TRP channels are activated by a variety of different stimuli and function as signal integrators. The TRP superfamily is divided into seven subfamilies: the five group 1 TRPs (TRPC, TRPV, TRPM, TRPN, and TRPA) and two group 2 subfamilies (TRPP and TRPML). TRP channels are important for human health as mutations in at least four TRP channels underlie disease.
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              STIM is a Ca2+ sensor essential for Ca2+-store-depletion-triggered Ca2+ influx.

              Ca(2+) signaling in nonexcitable cells is typically initiated by receptor-triggered production of inositol-1,4,5-trisphosphate and the release of Ca(2+) from intracellular stores. An elusive signaling process senses the Ca(2+) store depletion and triggers the opening of plasma membrane Ca(2+) channels. The resulting sustained Ca(2+) signals are required for many physiological responses, such as T cell activation and differentiation. Here, we monitored receptor-triggered Ca(2+) signals in cells transfected with siRNAs against 2,304 human signaling proteins, and we identified two proteins required for Ca(2+)-store-depletion-mediated Ca(2+) influx, STIM1 and STIM2. These proteins have a single transmembrane region with a putative Ca(2+) binding domain in the lumen of the endoplasmic reticulum. Ca(2+) store depletion led to a rapid translocation of STIM1 into puncta that accumulated near the plasma membrane. Introducing a point mutation in the STIM1 Ca(2+) binding domain resulted in prelocalization of the protein in puncta, and this mutant failed to respond to store depletion. Our study suggests that STIM proteins function as Ca(2+) store sensors in the signaling pathway connecting Ca(2+) store depletion to Ca(2+) influx.
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                Author and article information

                Journal
                Int J Cancer
                Int. J. Cancer
                10.1002/(ISSN)1097-0215
                IJC
                International Journal of Cancer
                John Wiley and Sons Inc. (Hoboken )
                0020-7136
                1097-0215
                29 September 2015
                01 May 2016
                : 138
                : 9 ( doiID: 10.1002/ijc.v138.9 )
                : 2067-2077
                Affiliations
                [ 1 ] Laboratory of Cancer BiologyInstitute of Clinical Science, Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University Hangzhou ZhejiangChina
                [ 2 ] Department of Medical Oncology, Sir Run Run Shaw HospitalCollege of Medicine, Zhejiang University Hangzhou ZhejiangChina
                [ 3 ]Center for Translational Cancer Research, Institute of Biosciences and Technology, Texas A&M University Health Science Center Houston TX
                Author notes
                [*] [* ] Correspondence to: Weidong Han, Laboratory of Cancer Biology, Institute of Clinical Science, Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University, Hangzhou, Zhejiang, China, Tel.: +86‐571‐86006926, Fax: +86‐571‐86044817, E‐mail: hanwd@ 123456zju.edu.cn or Yubin Zhou, Center for Translational Cancer Research, Institute of Biosciences and Technology, Texas a&M University Health Science Center, Houston, TX 77030, USA, E‐mail: yubinzhou@ 123456tamu.edu
                [†]

                J.X. and H.P. contributed equally to this work

                Article
                IJC29840
                10.1002/ijc.29840
                4764496
                26355642
                c20f5fcc-cac6-4a53-a4ec-1ed397e3eda0
                © 2015 The Authors International Journal of Cancer published by John Wiley & Sons Ltd on behalf of UICC

                This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 12 April 2015
                : 03 September 2015
                Page count
                Pages: 11
                Funding
                Funded by: National Natural Science Foundation of China
                Award ID: 81272593
                Award ID: NSFC‐81372621, 81572361
                Funded by: National Institutes of Health
                Award ID: R01GM112003
                Categories
                Mini Review
                Mini Review
                Custom metadata
                2.0
                ijc29840
                1 May 2016
                Converter:WILEY_ML3GV2_TO_NLMPMC version:4.9.4 mode:remove_FC converted:12.09.2016

                Oncology & Radiotherapy
                soce,stim1,orai1,cancer,calcium,therapeutics
                Oncology & Radiotherapy
                soce, stim1, orai1, cancer, calcium, therapeutics

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