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DNA Damage and Cytokine Production in Non-Target Irradiated Lymphocytes

机译:非目标辐照淋巴细胞中的DNA损伤和细胞因子产生

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In advanced radiotherapy, treatment of the tumor with high-intensity modulated fields is balanced with normal tissue sparing. However, the non-target dose delivered to surrounding healthy tissue within the irradiated volume is a potential cause for concern. Whether the effects observed are caused after exposure to out-of-field radiation or bystander effects through neighboring irradiated cells is not fully understood. The goal of this study was to determine the effect of exposure to out-of-field radiation in lymphocyte cell lines and primary blood cells. The role of cellular radiosensitivity in altering bystander responses in out-of-field exposed cells was also investigated. Target cells were positioned in a phantom in the center of the radiation field (in-field dose) and exposed to 2 Gy irradiation. Lymphocyte cell lines (C1, AT3ABR, Jurkat, THP-1, AT2Bi and AT3Bi) and peripheral blood were placed 1 cm away from the radiation field edge (out-of-field dose) and received an average dose of 10.8 +/- 4.2 cGy. Double-stranded DNA damage, cell growth and gene expression were measured in the out-of-field cells. Radiosensitive AT3ABR and primary blood cells demonstrated the largest increase in gamma-H2AX foci after irradiation. Exposure of normal cells to bystander factors from irradiated radiosensitive cell lines also increased DNA damage. Expression of IL-1, IL-6, TNF alpha and TGF beta after addition of bystander factors from radiosensitive cells showed differential effects in normally responding cells, with some evidence of an adaptive response observed. Exposure to out-of-field radiation induces DNA damage and reduces growth in radiosensitive cells. Bystander factors produced by directly irradiated cells in combination with out-of-field exposure may upregulate pro- and anti-inflammatory genes in responding cells of different radiosensitivities, with the potential of affecting the tumor microenvironment. A greater understanding of the radiobiological response in normal
机译:在晚期放疗中,用高强度调制场的肿瘤治疗与正常组织备件相平衡。然而,在照射体积内递送至周围健康组织的非靶剂剂量是潜在的担忧的潜在原因。观察到的效果是通过相邻辐照细胞暴露于场外辐射或旁观者效应之后是否引起的。本研究的目的是确定暴露于淋巴细胞细胞系和原发性血细胞的场外辐射的影响。还研究了细胞辐射敏感度在改变旁观者反应中的作用,还研究了在场外暴露细胞中的反应。将靶细胞定位在辐射场(野外剂量)的中心的虚线上,并暴露于2 Gy辐射。淋巴细胞系(C1,AT3ABR,Jurkat,THP-1,AT2BI和AT3BI)和外周血从辐射场边缘(外场剂量外)放置1cm,并接受10.8 +/- 4.2的平均剂量CGY。在外部细胞中测量双链DNA损伤,细胞生长和基因表达。辐射敏感性AT3ABR和初级血细胞显示出在照射后最大的γ-H2AX焦点增加。正常细胞暴露于来自辐射放射敏细胞系的旁观者因子也增加了DNA损伤。在从放射敏感细胞添加到旁观者因子后,IL-1,IL-6,TNFα和TGFβ的表达在通常响应细胞中显示出差异效应,观察到适应性反应的一些证据。暴露于场外辐射诱导DNA损伤并降低放射敏细胞的生长。通过直接照射细胞与外部曝光外暴露组合产生的旁观者因素可以提高抗炎症基因,在响应不同放射敏感度的细胞中,可能影响肿瘤微环境。对正常的辐射生物反应更加了解

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