Department of Radiation Oncology, Laboratory for Experimental Oncology and Radiobiology (LEXOR), Centre for Experimental Molecular Medicine, University of Amsterdam, P.O. Box 22700, 1100 DE Amsterdam, The Netherlands.
Oncol Rep. 2012 Mar;27(3):769-74. doi: 10.3892/or.2011.1604. Epub 2011 Dec 21.
Ionizing radiation-induced foci (IRIF) of DNA repair-related proteins accumulated at DNA double-strand break (DSB) sites have been suggested to be a powerful biodosimetric tool. However, the relationship between IRIF induction and biologically relevant endpoints, such as cell death and formation of chromosome rearrangements is less clear, especially for high linear energy transfer (LET) radiation. It is thus not sufficiently established whether IRIF are valid indicators of biological effectiveness of the various radiation types. This question is more significant in light of the recent advancements in light ion-beam and radionuclide therapy. Dose-effect relationships were determined for the induction of DNA-DSBs, chromosome aberrations and reproductive cell death in cultured SW-1573 cells irradiated with γ-rays from a Cs-137 source or with α-particles from an Am-241 source. Values of relative biological effectiveness (RBE) of the high LET α-particles were derived for these effects. DNA-DSB were detected by scoring of γ-H2AX foci, chromosome aberrations by fragments and translocations using premature chromosome condensation and cell survival by colony formation. Analysis of dose-effect relations was based on the linear-quadratic model. Except for the survival curves, for other effects no significant contribution was derived of the quadratic term in the range of doses up to 2 Gy of γ-rays. Calculated RBE values derived for the linear component of dose-effect relations for γ-H2AX foci, cell reproductive death, chromosome fragments and colour junctions are 1.0±0.3, 14.7±5.1, 15.3±5.9 and 13.3±6.0, respectively. RBE values calculated at a certain biological effect level are 1, 4, 13 and 13, respectively. The RBE values derived from the LQ model are preferred as they are based on clinically relevant doses. The results show that with low LET radiation only a small fraction of the numerous DNA-DSBs yield chromosome damage and reproductive cell death. It is concluded that many of the chromosomal aberrations detected by premature chromosome condensation do not cause reproductive cell death. Furthermore, RBE values for DNA-DSB detectable by γ-H2AX foci shortly after irradiation, provide no information relevant to applications of high LET radiation in radiotherapy. The RBE values of chromosome aberrations assessed by premature chromosome condensation are close to the value for reproductive cell death. This suggests possible relevance to assess RBE values for radiotherapy with high LET ions.
电离辐射诱导的 DNA 修复相关蛋白焦点(IRIF)在 DNA 双链断裂(DSB)位点的积累,已被认为是一种强大的生物剂量测定工具。然而,IRIF 的诱导与细胞死亡和染色体重排等生物学相关终点之间的关系尚不清楚,尤其是对于高线性能量转移(LET)辐射。因此,IRIF 是否是各种辐射类型生物学效应的有效指标尚不确定。鉴于最近在轻离子束和放射性核素治疗方面的进展,这个问题更加重要。用 Cs-137 源的γ射线或 Am-241 源的α粒子照射培养的 SW-1573 细胞,确定了诱导 DNA-DSB、染色体畸变和生殖细胞死亡的剂量效应关系。推导出了这些效应的高 LET α 粒子的相对生物效应(RBE)值。通过γ-H2AX 焦点的评分检测 DNA-DSB,用早熟染色体凝聚检测染色体畸变,用集落形成检测细胞存活。剂量效应关系的分析基于线性二次模型。除了存活曲线外,在高达 2Gy 的 γ 射线剂量范围内,其他效应的二次项没有显著贡献。对于 γ-H2AX 焦点、细胞生殖死亡、染色体片段和颜色连接的剂量效应关系线性分量推导的计算 RBE 值分别为 1.0±0.3、14.7±5.1、15.3±5.9 和 13.3±6.0。在特定生物学效应水平计算的 RBE 值分别为 1、4、13 和 13。基于临床相关剂量的 LQ 模型推导的 RBE 值更受青睐。结果表明,对于低 LET 辐射,只有少数大量的 DNA-DSB 产生染色体损伤和生殖细胞死亡。因此,可以得出结论,通过早熟染色体凝聚检测到的许多染色体畸变不会导致生殖细胞死亡。此外,照射后不久通过γ-H2AX 焦点检测到的 DNA-DSB 的 RBE 值并不能提供与高 LET 辐射在放射治疗中的应用相关的信息。通过早熟染色体凝聚评估的染色体畸变的 RBE 值接近生殖细胞死亡的 RBE 值。这表明对于使用高 LET 离子进行放射治疗评估 RBE 值可能具有相关性。