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首页> 外文期刊>Radiation Research: Official Organ of the Radiation Research Society >Modeling multicellular response to nonuniform distributions of radioactivity: Differences in cellular response to self-dose and cross-dose
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Modeling multicellular response to nonuniform distributions of radioactivity: Differences in cellular response to self-dose and cross-dose

机译:模拟对放射性不均匀分布的多细胞反应:细胞对自剂量和交叉剂量的反应差异

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Radiopharmaceuticals are distributed nonuniformly in tissue. While distributions of radioactivity often appear uniform at the organ level, in fact, microscopic examination reveals that only a fraction of the cells in tissue are labeled. Labeled cells and unlabeled cells often receive different absorbed doses depending on the extent of the nonuniformity and the characteristics of the emitted radiations. The labeled cells receive an absorbed dose from radioactivity within the cell (self-dose) as well as an absorbed dose from radioactivity in surrounding labeled cells (cross-dose). Unlabeled cells receive only a cross-dose. In recent communications, a multicellular cluster model was used to investigate the lethality of microscopic nonuniform distributions of I-131 iododeoxyuridine ((131)IdU). For a given mean absorbed dose to the tissue, the dose response depended on the percentage of cells that were labeled. Specifically, when 1, 10 and 100% of the cells were labeled, a D-37 of 6.4, 5.7 and 4.5 Gy, respectively, was observed. The reason for these differences was recently traced to differences in the cellular response to the self- and cross-doses delivered by (131)IdU. Systematic isolation of the effects of self-dose resulted in a D-37 of 1.2 +/- 0.3 Gy. The cross-dose component yielded a D-37 of 6.4 +/- 0.5 Gy. In the present work, the overall survival of multicellular clusters containing 1, 10 and 100% labeled cells is modeled using a semi-empirical approach that uses the mean lethal self- and cross-doses and the fraction of cells labeled. There is excellent agreement between the theoretical model and the experimental data when the surviving fraction is greater than 1%. Therefore, when the distribution of I-131 in tissue is nonuniform at the microscopic level, and the cellular response to self- and cross-doses differs, multicellular dosimetry can be used successfully to predict biological response, whereas the mean absorbed dose fails in this regard. (C) 2005 by Radiation Research Society.
机译:放射性药物在组织中的分布不均匀。尽管放射线的分布通常在器官水平上看起来很均匀,但实际上,显微镜检查显示组织中只有一部分细胞被标记。标记的细胞和未标记的细胞通常会根据不均匀程度和发射辐射的特性而接受不同的吸收剂量。标记的细胞从细胞内的放射性吸收剂量(自身剂量),以及周围标记的细胞中的放射性吸收剂量(交叉剂量)。未标记的细胞仅接受交叉剂量。在最近的通信中,使用多细胞簇模型研究I-131碘脱氧尿苷((131)IdU)的微观非均匀分布的致死性。对于给定的组织平均吸收剂量,剂量反应取决于标记细胞的百分比。具体地,当标记1、10和100%的细胞时,观察到D-37分别为6.4、5.7和4.5Gy。这些差异的原因最近被追溯到细胞对(131)IdU传递的自身和交叉剂量反应的差异。系统隔离自身剂量的作用导致D-37为1.2 +/- 0.3 Gy。跨剂量成分产生的D-37为6.4 +/- 0.5 Gy。在目前的工作中,使用半经验方法对包含1、10和100%标记细胞的多细胞簇的总体存活率进行建模,该方法使用平均致死性自身剂量和交叉剂量以及标记细胞的分数。当存活率大于1%时,理论模型与实验数据之间存在极好的一致性。因此,当I-131在组织中的分布在微观水平上是不均匀的,并且细胞对自身和交叉剂量的反应有所不同时,多细胞剂量法可以成功地用于预测生物学反应,而平均吸收剂量在这种情况下会失败看待。 (C)2005年,辐射研究学会。

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