Zeiss Caroline J, Johnson Linda K
Yale University School of Medicine, New Haven, Connecticut. University of Colorado, Anschutz Medical Campus in Aurora, Colorado.
ILAR J. 2017 Jul 1;58(1):1-3. doi: 10.1093/ilar/ilx017.
Animal research has constituted a fundamental means to achieve groundbreaking therapies for human disease. However, for complex diseases, promising preclinical results have failed to translate to the clinic. Reasons for this disparity are multifactorial. These include the challenges inherent in modeling complex disease in animals, as well issues of study design, reproducibility and operational norms within the biomedical research enterprise. In this issue, we explore the range of information resources available for the comparative study of disease, as well as challenges to the ultimate translation of preclinical findings. Genomics resources in support of translational research are described for zebrafish, mice, rats and non-human primates. The utility of transcriptomics to explore the temporal basis of lesion development in toxicologic pathology is reviewed. Integration of the ever-increasing volume of text-based and bioinformatics data is a significant challenge, and in this issue, informatics resources and general text mining methodologies to explore and aggregate text data are described. Finally, factors contributing to both reproducibility and translatability are examined. Guidelines designed to address reproducibility are essential to improving individual studies. To this end, a viewpoint from the National Institutes of Health on measures needed to enhance rigor and reproducibility is given, as well as an overview of the role of the Institutional Animal Care and Use Committee in this regard. The challenge of improving generalizability of animal experiments so that their findings can be more frequently extended to the intended human population remains. Reasons why models that replicate key aspects of human disease fail to be predictive in humans are explored in two fields in which translation has been a challenge: sepsis and neurodegeneration.
动物研究一直是实现人类疾病突破性治疗方法的基本手段。然而,对于复杂疾病而言,有前景的临床前研究结果却未能转化为临床应用。造成这种差异的原因是多方面的。这些原因包括在动物身上模拟复杂疾病所固有的挑战,以及生物医学研究领域内的研究设计、可重复性和操作规范等问题。在本期中,我们探讨了可用于疾病比较研究的一系列信息资源,以及临床前研究结果最终转化面临的挑战。介绍了支持斑马鱼、小鼠、大鼠和非人类灵长类动物转化研究的基因组学资源。回顾了转录组学在毒理病理学中探索病变发展时间基础方面的应用。整合不断增加的基于文本和生物信息学的数据是一项重大挑战,在本期中,描述了用于探索和汇总文本数据的信息学资源和一般文本挖掘方法。最后,研究了影响可重复性和可转化性的因素。旨在解决可重复性问题的指南对于改进个体研究至关重要。为此,给出了美国国立卫生研究院关于提高严谨性和可重复性所需措施的观点,以及机构动物护理和使用委员会在这方面的作用概述。提高动物实验普遍性以使研究结果更频繁地推广到目标人群的挑战依然存在。在脓毒症和神经退行性变这两个转化面临挑战的领域中,探讨了复制人类疾病关键方面的模型在人类中无法进行预测的原因。