Koontz Bridget F, Verhaegen Frank, De Ruysscher Dirk
1 Department of Radiation Oncology, Duke Cancer Institute, Durham, NC, USA.
2 Department of Radiation Oncology (MAASTRO), GROW-School for Oncology and Developmental Biology, Maastricht University Medical Centre, Maastricht, Netherlands.
Br J Radiol. 2017 Jan;90(1069):20160441. doi: 10.1259/bjr.20160441. Epub 2016 Sep 26.
Animal modelling is essential to the study of radiobiology and the advancement of clinical radiation oncology by providing preclinical data. Mouse models in particular have been highly utilized in the study of both tumour and normal tissue radiobiology because of their cost effectiveness and versatility. Technology has significantly advanced in preclinical radiation techniques to allow highly conformal image-guided irradiation of small animals in an effort to mimic human treatment capabilities. However, the biological and physical limitations of animal modelling should be recognized and considered when interpreting preclinical radiotherapy (RT) studies. Murine tumour and normal tissue radioresponse has been shown to vary from human cellular and molecular pathways. Small animal irradiation techniques utilize different anatomical boundaries and may have different physical properties than human RT. This review addresses the difference between the human condition and mouse models and discusses possible strategies for future refinement of murine models of cancer and radiation for the benefit of both basic radiobiology and clinical translation.
动物建模通过提供临床前数据,对于放射生物学研究和临床放射肿瘤学的进展至关重要。特别是小鼠模型,因其成本效益和多功能性,在肿瘤和正常组织放射生物学研究中得到了高度利用。临床前放射技术有了显著进步,能够对小动物进行高度适形的图像引导照射,以努力模拟人类治疗能力。然而,在解释临床前放射治疗(RT)研究时,应认识并考虑动物建模的生物学和物理局限性。已表明小鼠肿瘤和正常组织的放射反应与人类细胞和分子途径不同。小动物照射技术利用不同的解剖边界,并且可能具有与人类放疗不同的物理特性。本综述阐述了人类情况与小鼠模型之间的差异,并讨论了未来优化癌症和放射小鼠模型的可能策略,以造福基础放射生物学和临床转化。