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Reduced High-Dose Radiation-Induced Residual Genotoxic Damage by Induction of Radioadaptive Response and Prophylactic Mild Dietary Restriction in Mice

机译:通过诱导小鼠的放射性反应和预防性轻度膳食限制降低高剂量辐射诱导的残留遗传毒性损伤

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摘要

Radioadaptive response (RAR) describes a phenomenon in a variety of in vitro and in vivo systems that a low-dose of priming ionizing radiation (IR) reduces detrimental effects of a subsequent challenge IR at higher doses. Among in vivo investigations, studies using the mouse RAR model (Yonezawa Effect) showed that RAR could significantly extenuate high-dose IR-induced detrimental effects such as decrease of hematopoietic stem cells and progenitor cells, acute radiation hematopoietic syndrome, genotoxicity and genomic instability. Meanwhile, it has been demonstrated that diet intervention has a great impact on health, and dietary restriction shows beneficial effects on numerous diseases in animal models. In this work, by using the mouse RAR model and mild dietary restriction (MDR), we confirmed that combination of RAR and MDR could more efficiently reduce radiogenotoxic damage without significant change of the RAR phenotype. These findings suggested that MDR may share some common pathways with RAR to activate mechanisms consequently resulting in suppression of genotoxicity. As MDR could also increase resistance to chemotherapy and radiotherapy in normal cells, we propose that combination of MDR, RAR, and other cancer treatments (i.e., chemotherapy and radiotherapy) represent a potential strategy to increase the treatment efficacy and prevent IR risk in humans.
机译:Radioadapptive反应(RAR)描述了各种体外和体内系统中的现象,即低剂量的灌注电离辐射(IR)降低了随后的攻击IR处于更高剂量的不利影响。在体内调查中,使用小鼠RAR模型(​​Yonezawa效应)的研究表明,RAR可以显着地显着扩展高剂量IR诱导的有害效果,例如造血干细胞和祖细胞的降低,急性辐射造血综合征,遗传毒性和基因组不稳定性。同时,已经证明饮食干预对健康产生了很大影响,饮食限制对动物模型的众多疾病表现出有益的影响。在这项工作中,通过使用鼠标RAR模型和温和的饮食限制(MDR),我们证实RAR和MDR的组合可以更有效地降低放射毒性损伤,而无需RAR表型的显着变化。这些发现表明,MDR可以与RAR共享一些常见的途径,以激活机制,从而导致抑制基因毒性。由于MDR还可以在正常细胞中增加对化疗和放射疗法的抵抗力,我们提出了MDR,RAR和其他癌症处理的组合(即化疗和放射治疗)代表了增加治疗疗效和防止人类的IR风险的潜在策略。

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