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Finding the Genetic Determinants of Adverse Reactions toRadiotherapy

机译:寻找放疗不良反应的遗传决定因素

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Individual variation in radiosensitivity is thought to be at least partly determined by genetic factors. The remaining difference between individuals is caused by comorbidities, variation in treatment, body habitus and stochastic factors. Evidence for the heritability of radiosensitivity comes from rare genetic disorders and from cell-based studies. To what extent common and rare genetic variants might explain the genetic component of radiosensitivity has not been fully elucidated. If the genetic variants accounting for this heritability were to be determined, they could be incorporated into any future predictive statistical model of adverse reactions to radiotherapy. With the evolution of DNA sequencing and bioinformatics, radiogenomics has emerged as a new research field with the aim of finding the genetic determinants of adverse reactions to radiotherapy. Similar to the investigation of other complex genetic disease traits, early studies in radiogenomics involved candidate gene association studies - many plagued by false associations caused by low sample sizes and problematic experimental design. More recently, some promising genetic associations (e.g. with tumour necrosis factor) have emerged from large multi-institutional cohorts with built-in replication. At the same time, several small- to medium-sized genome-wide association studies (GWAS) have been or are about to be published. These studies will probably lead to an increasing number of genetic polymorphisms that may predict adverse reactions to radiotherapy. The future of the field is to create large patient cohorts for multiple cancer types, to validate the genetic loci and build reliable predictive models. For example, the REQUITE project involves multiple groups in Europe and North America. For further discovery studies, larger GWAS will be necessary to include rare sequence variants through next generation sequencing. Ultimately, radiogenomics seeks to predict which cancer patients will show radiosensitivity or radioresistance, so oncologists and surgeons can alter treatment accordingly to lower adverse reactions or increase the efficacy of radiotherapy.
机译:人们认为放射敏感性的个体差异至少部分地由遗传因素决定。个体之间的剩余差异是由合并症,治疗差异,身体习惯和随机因素引起的。放射敏感性的遗传力证据来自罕见的遗传疾病和基于细胞的研究。普通和稀有的遗传变异在多大程度上可以解释放射敏感性的遗传成分尚未完全阐明。如果要确定可解释这种遗传性的遗传变异,则可以将其纳入未来对放射疗法不良反应的任何预测性统计模型中。随着DNA测序和生物信息学的发展,放射基因组学已经成为一个新的研究领域,其目的是寻找对放射治疗不良反应的遗传决定因素。与其他复杂遗传疾病特征的研究相似,放射性基因组学的早期研究涉及候选基因关联研究-许多受样本数量低和实验设计问题引起的错误关联困扰。最近,从具有内置复制的大型多机构队列中出现了一些有希望的遗传关联(例如,与肿瘤坏死因子相关)。同时,一些中小型全基因组关联研究(GWAS)已经或即将出版。这些研究可能会导致越来越多的遗传多态性可以预测放疗的不良反应。该领域的未来是为多种癌症类型创建大型患者队列,以验证遗传基因座并建立可靠的预测模型。例如,REQUITE项目涉及欧洲和北美的多个小组。对于进一步的发现研究,将需要更大的GWAS,以通过下一代测序来包含稀有序列变体。最终,放射基因组学试图预测哪些癌症患者将表现出放射敏感性或放射抵抗性,因此肿瘤科医生和外科医生可以相应地改变治疗方法,以降低不良反应或提高放射治疗的效率。

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