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超竞争作为辐射致癌中剂量率效应的一种新机制:数学模型研究

Super-competition as a Novel Mechanism of the Dose-rate Effect in Radiation Carcinogenesis: A Mathematical Model Study.

作者信息

Hattori Yuya, Nagata Kento, Watanabe Ritsuko, Yokoya Akinari, Imaoka Tatsuhiko

机构信息

Faculty of Electrical Engineering and Information Science, National Institute of Technology Kure College, Hiroshima 737-8506 Japan.

Department of Radiation Effects Research, Institute for Radiological Science, National Institutes for Quantum Science and Technology, Chiba-shi, Chiba 263-8555, Japan.

出版信息

Radiat Res. 2025 Feb 1;203(2):61-72. doi: 10.1667/RADE-24-00191.1.

Abstract

Data from animal experiments show that the radiation-related risk of cancer decreases if the dose rate is reduced, even though the cumulative dose is unchanged (i.e., a dose-rate effect); however, the underlying mechanism is not well understood. To explore factors underlying the dose-rate effect observed in experimental rat mammary carcinogenesis, we developed a mathematical model that accounts for cellular dynamics during carcinogenesis, and then examined whether the model predicts cancer incidence. A mathematical model of multistage carcinogenesis involving radiation-induced cell death and mutagenesis was constructed using differential equations. The mutation rate was changed depending on the dose rate. The model also considered competition among cells with various mutation levels. The main parameters of the model were determined using previous experimental data. The parameters of the model were consistent with experimental observations. A dose-rate effect on carcinogenesis became apparent when the relationship between dose rate and mutation rate was linear quadratic or quadratic. The dose-rate effect became prominent when cells with more mutations preferentially compensated for the radiation-induced death of cells with fewer mutations. The phenomenon by which mutated cells gain a competitive advantage over normal cells is known as super-competition. Here, we identified super-competition as a novel mechanism underlying the dose-rate effects on carcinogenesis. The data also confirmed the relevance of the shape of the relationship between dose rate and the mutation rate. Thus, this study provides new evidence for the mechanism underlying the dose-rate effect, which is important for predicting the cancer-related risks of low-dose-rate irradiation.

摘要

动物实验数据表明,即使累积剂量不变,降低剂量率也会降低辐射相关的癌症风险(即剂量率效应);然而,其潜在机制尚未完全明确。为了探究实验性大鼠乳腺癌发生过程中观察到的剂量率效应背后的因素,我们建立了一个数学模型来解释癌症发生过程中的细胞动态变化,然后检验该模型是否能预测癌症发病率。利用微分方程构建了一个涉及辐射诱导细胞死亡和诱变的多阶段癌症发生数学模型。突变率根据剂量率而变化。该模型还考虑了不同突变水平细胞之间的竞争。模型的主要参数根据先前的实验数据确定。模型参数与实验观察结果一致。当剂量率与突变率的关系为线性二次或二次关系时,剂量率对癌症发生的效应变得明显。当具有更多突变的细胞优先补偿辐射诱导的较少突变细胞的死亡时,剂量率效应变得显著。突变细胞相对于正常细胞获得竞争优势的现象被称为超竞争。在此,我们确定超竞争是剂量率对癌症发生效应的一种新机制。数据还证实了剂量率与突变率关系形状的相关性。因此,本研究为剂量率效应的潜在机制提供了新证据,这对于预测低剂量率辐射的癌症相关风险具有重要意义。

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