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Short DNA Fragments Are a Hallmark of Heavy Charged-Particle Irradiation and May Underlie Their Greater Therapeutic Efficacy

机译:短的DNA片段是重度带电粒子辐照的标志可能是其更大的治疗功效的基础

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摘要

Growing interest in proton and heavy ion therapy has reinvigorated research into the fundamental biological mechanisms underlying the therapeutic efficacy of charged-particle radiation. To improve our understanding of the greater biological effectiveness of high-LET radiations, we have investigated DNA double-strand breaks (DSBs) following exposure of plasmid DNA to low-LET Co-60 gamma photon and electron irradiation and to high-LET Beryllium and Argon ions with atomic force microscopy. The sizes of DNA fragments following radiation exposure were individually measured to construct fragment size distributions from which the DSB per DNA molecule and DSB spatial distributions were derived. We report that heavy charged particles induce a significantly larger proportion of short DNA fragments in irradiated DNA molecules, reflecting densely and clustered damage patterns of high-LET energy depositions. We attribute the enhanced short DNA fragmentation following high-LET radiations as an important determinant of the observed, enhanced biological effectiveness of high-LET irradiations.
机译:对质子和重离子疗法的兴趣日益浓厚,重新激发了对带电粒子辐射治疗功效的基本生物学机制的研究。为了提高我们对高LET辐射的更大生物学功效的理解,我们研究了将质粒DNA暴露于低LET Co-60γ光子和电子辐射以及高LET铍和高剂量铍后的DNA双链断裂(DSB)。原子力显微镜下的氩离子。分别测量辐射照射后DNA片段的大小,以构建片段大小分布,从中得出每个DNA分子的DSB和DSB空间分布。我们报告说,重的带电粒子在被辐照的DNA分子中诱导了较大比例的短DNA片段,反映了高LET能量沉积的密集和聚集损伤模式。我们将高LET辐射后增强的短DNA片段化归因于高LET辐射观察到的增强生物有效性的重要决定因素。

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