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Integration of Principles of Systems Biology and Radiation Biology: Toward Development of in silico Models to Optimize IUdR-Mediated Radiosensitization of DNA Mismatch Repair Deficient (Damage Tolerant) Human Cancers

机译:整合系统生物学和辐射生物学原理:朝着计算机模型的发展,以优化IUdR介导的DNA错配修复缺陷(耐受损伤)人类癌症的放射敏化。

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摘要

Over the last 7 years, we have focused our experimental and computational research efforts on improving our understanding of the biochemical, molecular, and cellular processing of iododeoxyuridine (IUdR) and ionizing radiation (IR) induced DNA base damage by DNA mismatch repair (MMR). These coordinated research efforts, sponsored by the National Cancer Institute Integrative Cancer Biology Program (ICBP), brought together system scientists with expertise in engineering, mathematics, and complex systems theory and translational cancer researchers with expertise in radiation biology. Our overall goal was to begin to develop computational models of IUdR- and/or IR-induced base damage processing by MMR that may provide new clinical strategies to optimize IUdR-mediated radiosensitization in MMR deficient (MMR−) “damage tolerant” human cancers. Using multiple scales of experimental testing, ranging from purified protein systems to in vitro (cellular) and to in vivo (human tumor xenografts in athymic mice) models, we have begun to integrate and interpolate these experimental data with hybrid stochastic biochemical models of MMR damage processing and probabilistic cell cycle regulation models through a systems biology approach. In this article, we highlight the results and current status of our integration of radiation biology approaches and computational modeling to enhance IUdR-mediated radiosensitization in MMR− damage tolerant cancers.
机译:在过去的7年中,我们集中进行了实验和计算研究工作,以加深对碘脱氧尿苷(IUdR)的生物化学,分子和细胞加工以及电离辐射(IR)引起的DNA错配修复(MMR)引起的DNA碱基损伤的了解。 。由美国国家癌症研究所综合癌症生物学计划(ICBP)赞助的这些协调的研究工作将在工程,数学和复杂系统理论方面具有专长的系统科学家与在放射生物学方面具有专长的转化癌症研究人员聚集在一起。我们的总体目标是开始开发MMR对IUdR和/或IR诱导的碱基损伤处理的计算模型,该模型可以提供新的临床策略,以优化MMd缺陷(MMR-)“损伤耐受”人类癌症中IUdR介导的放射增敏作用。从纯化的蛋白质系统到体外(细胞)和体内(无胸腺小鼠的人类肿瘤异种移植物)模型,我们使用了多种规模的实验测试,我们已经开始将这些实验数据与MMR损伤的混合随机生化模型进行整合和插值系统生物学方法处理和概率性细胞周期调控模型。在本文中,我们重点介绍了放射生物学方法和计算模型集成的结果和当前状态,以增强IUdR介导的MMR损伤耐受性癌症的放射增敏作用。

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