Department of Oncology, Aarhus University Hospital, Denmark; Department of Experimental Clinical Oncology, Aarhus University Hospital, Denmark.
Department of Experimental Clinical Oncology, Aarhus University Hospital, Denmark.
Cancer Lett. 2016 Nov 1;382(1):127-136. doi: 10.1016/j.canlet.2016.01.035. Epub 2016 Jan 28.
Radiogenomics designates a scientific field that addresses possible associations between genetic germline alterations and normal tissue toxicity after radiotherapy. The ultimate aim of this research is to establish a gene-based predictive test for normal tissue radiosensitivity. During the last 5 years, substantial progress has been achieved in this field. Several compelling associations for SNPs have been demonstrated in large candidate gene studies as well as genome wide association studies. These findings shed new light on radiobiology and expand our understanding of the processes that lead to side effects after radiotherapy. Despite this, certain fundamental challenges still relate to genomic approaches. Based on the latest insights into complex trait genetics and molecular genetics, we provide an analysis of these challenges and propose putative strategies to further advance the field. These strategies include 'big data approaches' and collaborative research within international consortia. Furthermore, research that combines the study of radiation-induced gene expression and genome-wide SNP genotype may discover genetic alterations that regulate the biological response to ionizing radiation. Thus, such integrative approaches may lead to genetic alterations that affect risk of normal tissue toxicity.
放射基因组学指定了一个科学领域,该领域涉及遗传种系改变与放射治疗后正常组织毒性之间可能存在的关联。这项研究的最终目的是建立一种基于基因的正常组织放射敏感性预测测试。在过去的 5 年中,该领域取得了实质性的进展。在大型候选基因研究和全基因组关联研究中,已经证明了几个令人信服的 SNP 关联。这些发现为放射生物学提供了新的视角,并扩展了我们对导致放射治疗后副作用的过程的理解。尽管如此,某些基本挑战仍然与基因组方法有关。基于对复杂特征遗传学和分子遗传学的最新见解,我们对这些挑战进行了分析,并提出了进一步推进该领域的假设策略。这些策略包括“大数据方法”和国际联盟内的合作研究。此外,将辐射诱导的基因表达研究与全基因组 SNP 基因型相结合的研究可能会发现调节对电离辐射的生物学反应的遗传改变。因此,这种综合方法可能会导致影响正常组织毒性风险的遗传改变。