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      Bystander effectors of chondrosarcoma cells irradiated at different LET impair proliferation of chondrocytes

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          Abstract

          While the dose-response relationship of radiation-induced bystander effect (RIBE) is controversial at low and high linear energy transfer (LET), mechanisms and effectors of cell-to-cell communication stay unclear and highly dependent of cell type. In the present study, we investigated the capacity of chondrocytes in responding to bystander factors released by chondrosarcoma cells irradiated at different doses (0.05 to 8 Gy) with X-rays and C-ions. Following a medium transfer protocol, cell survival, proliferation and DNA damages were quantified in bystander chondrocytes. The bystander factors secreted by chondrosarcoma cells were characterized. A significant and major RIBE response was observed in chondrocyte cells (T/C-28a2) receiving conditioned medium from chondrosarcoma cells (SW1353) irradiated with 0.1 Gy of X-rays and 0.05 Gy of C-ions, resulting in cell survivals of 36% and 62%, respectively. Micronuclei induction in bystander cells was observed from the same low doses. The cell survival results obtained by clonogenic assays were confirmed using impedancemetry. The bystander activity was vanished after a heat treatment or a dilution of the conditioned media. The cytokines which are well known as bystander factors, TNF-α and IL-6, were increased as a function of doses and LET according to an ELISA multiplex analysis. Together, the results demonstrate that irradiated chondrosarcoma cells can communicate stress factors to non-irradiated chondrocytes, inducing a wide and specific bystander response related to both doses and LET.

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          Persistent DNA damage signaling triggers senescence-associated inflammatory cytokine secretion

          Cellular senescence suppresses cancer by stably arresting the proliferation of damaged cells1. Paradoxically, senescent cells also secrete factors that alter tissue microenvironments2. The pathways regulating this secretion are unknown. We show that damaged human cells develop persistent chromatin lesions bearing hallmarks of DNA double-strand breaks (DSBs), which initiate increased secretion of inflammatory cytokines such as interleukin-6 (IL-6). Cytokine secretion occurred only after establishment of persistent DNA damage signaling, usually associated with senescence, not after transient DNA damage responses (DDR). Initiation and maintenance of this cytokine response required the DDR proteins ATM, NBS1 and CHK2, but not the cell cycle arrest enforcers p53 and pRb. ATM was also essential for IL-6 secretion during oncogene-induced senescence and by damaged cells that bypass senescence. Further, DDR activity and IL-6 were elevated in human cancers, and ATM-depletion suppressed the ability of senescent cells to stimulate IL-6-dependent cancer cell invasiveness. Thus, in addition to orchestrating cell cycle checkpoints and DNA repair, a novel and important role of the DDR is to allow damaged cells to communicate their compromised state to the surrounding tissue.
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            Carbon ion radiotherapy in Japan: an assessment of 20 years of clinical experience.

            Charged particle therapy is generally regarded as cutting-edge technology in oncology. Many proton therapy centres are active in the USA, Europe, and Asia, but only a few centres use heavy ions, even though these ions are much more effective than x-rays owing to the special radiobiological properties of densely ionising radiation. The National Institute of Radiological Sciences (NIRS) Chiba, Japan, has been treating cancer with high-energy carbon ions since 1994. So far, more than 8000 patients have had this treatment at NIRS, and the centre thus has by far the greatest experience in carbon ion treatment worldwide. A panel of radiation oncologists, radiobiologists, and medical physicists from the USA and Europe recently completed peer review of the carbon ion therapy at NIRS. The review panel had access to the latest developments in treatment planning and beam delivery and to all updated clinical data produced at NIRS. A detailed comparison with the most advanced results obtained with x-rays or protons in Europe and the USA was then possible. In addition to those tumours for which carbon ions are known to produce excellent results, such as bone and soft-tissue sarcoma of the skull base, head and neck, and pelvis, promising data were obtained for other tumours, such as locally recurrent rectal cancer and pancreatic cancer. The most serious impediment to the worldwide spread of heavy ion therapy centres is the high initial capital cost. The 20 years of clinical experience at NIRS can help guide strategic decisions on the design and construction of new heavy ion therapy centres. Copyright © 2015 Elsevier Ltd. All rights reserved.
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              Mechanism of radiation-induced bystander effects: a unifying model.

              The radiation-induced bystander effect represents a paradigm shift in our understanding of the radiobiological effects of ionizing radiation, in that extranuclear and extracellular events may also contribute to the final biological consequences of exposure to low doses of radiation. Although radiation-induced bystander effects have been well documented in a variety of biological systems, the mechanism is not known. It is likely that multiple pathways are involved in the bystander phenomenon, and different cell types respond differently to bystander signalling. Using cDNA microarrays, a number of cellular signalling genes, including cyclooxygenase-2 (COX-2), have been shown to be causally linked to the bystander phenomenon. The observation that inhibition of the phosphorylation of extracellular signal-related kinase (ERK) suppressed the bystander response further confirmed the important role of the mitogen-activated protein kinase (MAPK) signalling cascade in the bystander process. Furthermore, cells deficient in mitochondrial DNA showed a significantly reduced response to bystander signalling, suggesting a functional role of mitochondria in the signalling process. Inhibitors of nitric oxide (NO) synthase (NOS) and mitochondrial calcium uptake provided evidence that NO and calcium signalling are part of the signalling cascade. The bystander observations imply that the relevant target for various radiobiological endpoints is larger than an individual cell. A better understanding of the cellular and molecular mechanisms of the bystander phenomenon, together with evidence of their occurrence in-vivo, will allow us to formulate a more accurate model for assessing the health effects of low doses of ionizing radiation.
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                Author and article information

                Contributors
                +33 (0)231 454 564 , chevalier@ganil.fr , francois.chevalier@cea.fr
                Journal
                J Cell Commun Signal
                J Cell Commun Signal
                Journal of Cell Communication and Signaling
                Springer Netherlands (Dordrecht )
                1873-9601
                1873-961X
                22 March 2019
                22 March 2019
                September 2019
                : 13
                : 3
                : 343-356
                Affiliations
                [1 ]LARIA, iRCM, François Jacob Institute of biology, DRF-CEA, Caen, France
                [2 ]ISNI 0000 0001 2186 4076, GRID grid.412043.0, UMR6252 CIMAP, CEA - CNRS - ENSICAEN - Université de Caen Normandie, ; Caen, France
                [3 ]ISNI 0000 0000 9463 5349, GRID grid.443874.8, Department of Life and Environmental Physics, , Horia Hulubei National Institute of Physics and Nuclear Engineering, ; Reactorului 30, P.O. Box MG-6, 077125 Magurele, Romania
                [4 ]ISNI 0000 0001 2186 4076, GRID grid.412043.0, ImpedanCELL Platform, Federative Structure 4206 ICORE, Normandie Univ, UNICAEN, Inserm U1086 ANTICIPE « Interdisciplinary Research Unit for Cancer Prevention and Treatment », Biology and Innovative Therapeutics for Ovarian Cancers group (BioTICLA), Comprehensive Cancer Center F. Baclesse, ; 14000 Caen, France
                [5 ]ISNI 0000 0001 2285 8823, GRID grid.239915.5, Research Division, , Hospital for Special Surgery and Weill Cornell Medical College, ; New York, NY USA
                [6 ]GRID grid.462469.b, University of Montpellier, LBPC/PPC, IRMB, CHU de Montpellier, ; 34000 Montpellier, France
                [7 ]ISNI 0000 0000 9805 2626, GRID grid.250464.1, Cell Signal Unit, OIST, ; Onna-son, Okinawa, Japan
                [8 ]ISNI 0000 0001 2181 8731, GRID grid.419638.1, Dept. of Radiation Effects Research, NIRS, QST, ; Chiba-shi, Japan
                Author information
                http://orcid.org/0000-0002-8488-2324
                Article
                515
                10.1007/s12079-019-00515-9
                6732157
                30903603
                06936708-7d1c-48d8-97d5-131edb9e3cfe
                © The Author(s) 2019

                Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.

                History
                : 28 August 2018
                : 8 March 2019
                Funding
                Funded by: IRHEMME
                Award ID: Emergence 2015
                Funded by: FundRef http://dx.doi.org/10.13039/501100006289, Électricité de France;
                Categories
                Research Article
                Custom metadata
                © The International CCN Society 2019

                Cell biology
                chondrosarcoma,radiation-induced bystander effect,chondrocyte,high-let,low-dose irradiation

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