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      The force awakens: metastatic dormant cancer cells

      review-article
      1 , 2 , 1 , 2 ,
      Experimental & Molecular Medicine
      Nature Publishing Group UK
      Cancer microenvironment, Metastasis

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          Abstract

          Recurrent cancer that spreads to distant sites is the leading cause of disease-related death among cancer patients. Cancer cells are likely to disseminate during cancer progression, and some may enter dormancy, remaining viable but not increasing. These dormant cancer cells (DCCs) are rarely detectable with current diagnostic systems. Moreover, they can interpret homoeostatic signals from the microenvironment, thereby evading immune surveillance and chemotherapy. Eventually, DCCs can reawaken in response to signals, which are not yet fully understood, resulting in recurrence and metastasis. Therefore, understanding the biology of DCC reawakening is key to preventing metastasis. Over the last decade, a growing body of literature has revealed the mechanisms involved in cancer dormancy and reawakening. The cytotoxic activity of immune cells can cause cancer cells to enter a dormant state, and chronic inflammation can reactivate cancer proliferation at distant sites. Upon the binding of circulating DCCs to extracellular molecules, various signaling cascades are activated and reinitiate cell proliferation. In the present review, we attempt to consolidate the existing literature to provide a framework for the understanding of this crucial step in cancer progression.

          Cancer spread: How to let sleeping cells lie

          Preventing dormant cancer cells (DCCs) from reawakening could be key to preventing cancer recurrence. During cancer progression, dormant tumor cells can travel through the bloodstream, reawakening to form tumors in distant tissues. These tumors, known as metastases, are difficult to treat. The signals that cue DCCs to enter and exit dormancy are poorly understood. In a review, Jeong-Seok Nam and So-Yeon Park at the Gwangju Institute of Science and Technology in South Korea report that DCCs often enter dormancy to evade attack by immune cells. Once in a new location, DCCs receive signals from the surrounding tissue, which can trigger tumor development. DCCs can also be reactivated by chronic inflammation. Signals that block reactivation of DCCs are currently being tested as potential therapeutics, and may help in the fight against this leading cause of death from cancer.

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          Most cited references73

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          Tumor metastasis: molecular insights and evolving paradigms.

          Metastases represent the end products of a multistep cell-biological process termed the invasion-metastasis cascade, which involves dissemination of cancer cells to anatomically distant organ sites and their subsequent adaptation to foreign tissue microenvironments. Each of these events is driven by the acquisition of genetic and/or epigenetic alterations within tumor cells and the co-option of nonneoplastic stromal cells, which together endow incipient metastatic cells with traits needed to generate macroscopic metastases. Recent advances provide provocative insights into these cell-biological and molecular changes, which have implications regarding the steps of the invasion-metastasis cascade that appear amenable to therapeutic targeting. Copyright © 2011 Elsevier Inc. All rights reserved.
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            How ERK1/2 activation controls cell proliferation and cell death: Is subcellular localization the answer?

            Extracellular signal-regulated protein kinases 1 and 2 (ERK1/2) are members of the mitogen-activated protein kinase super family that can mediate cell proliferation and apoptosis. The Ras-Raf-MEK-ERK signaling cascade controlling cell proliferation has been well studied but the mechanisms involved in ERK1/2-mediated cell death are largely unknown. This review focuses on recent papers that define ERK1/2 translocation to the nucleus and the proteins involved in the cytosolic retention of activated ERK1/2. Cytosolic retention of ERK1/2 denies access to the transcription factor substrates that are responsible for the mitogenic response. In addition, cytosolic ERK1/2, besides inhibiting survival and proliferative signals in the nucleus, potentiates the catalytic activity of some proapoptotic proteins such as DAP kinase in the cytoplasm. Studies that further define the function of cytosolic ERK1/2 and its cytosolic substrates that enhance cell death will be essential to harness this pathway for developing effective treatments for cancer and chronic inflammatory diseases.
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              The role of cellular reactive oxygen species in cancer chemotherapy

              Most chemotherapeutics elevate intracellular levels of reactive oxygen species (ROS), and many can alter redox-homeostasis of cancer cells. It is widely accepted that the anticancer effect of these chemotherapeutics is due to the induction of oxidative stress and ROS-mediated cell injury in cancer. However, various new therapeutic approaches targeting intracellular ROS levels have yielded mixed results. Since it is impossible to quantitatively detect dynamic ROS levels in tumors during and after chemotherapy in clinical settings, it is of increasing interest to apply mathematical modeling techniques to predict ROS levels for understanding complex tumor biology during chemotherapy. This review outlines the current understanding of the role of ROS in cancer cells during carcinogenesis and during chemotherapy, provides a critical analysis of the methods used for quantitative ROS detection and discusses the application of mathematical modeling in predicting treatment responses. Finally, we provide insights on and perspectives for future development of effective therapeutic ROS-inducing anticancer agents or antioxidants for cancer treatment.
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                Author and article information

                Contributors
                namje@gist.ac.kr
                Journal
                Exp Mol Med
                Exp. Mol. Med
                Experimental & Molecular Medicine
                Nature Publishing Group UK (London )
                1226-3613
                2092-6413
                16 April 2020
                16 April 2020
                April 2020
                : 52
                : 4
                : 569-581
                Affiliations
                [1 ]ISNI 0000 0001 1033 9831, GRID grid.61221.36, School of Life Sciences, , Gwangju Institute of Science and Technology, ; Gwangju, 61005 Republic of Korea
                [2 ]ISNI 0000 0001 1033 9831, GRID grid.61221.36, Cell Logistics Research Center, , Gwangju Institute of Science and Technology, ; Gwangju, 61005 Republic of Korea
                Article
                423
                10.1038/s12276-020-0423-z
                7210927
                32300189
                1af8fa44-24a5-4aa5-9e00-d8c002c5c8fc
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 7 December 2019
                : 3 March 2020
                : 19 March 2020
                Funding
                Funded by: FundRef https://doi.org/10.13039/501100003725, National Research Foundation of Korea (NRF);
                Award ID: NRF-2016R1A5A1007318
                Award Recipient :
                Categories
                Review Article
                Custom metadata
                © The Author(s) 2020

                Molecular medicine
                cancer microenvironment,metastasis
                Molecular medicine
                cancer microenvironment, metastasis

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