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转录组学工具箱:在代谢性疾病动脉粥样硬化的精准医学背景下解读大型基因表达数据的资源

The Transcriptomic Toolbox: Resources for Interpreting Large Gene Expression Data within a Precision Medicine Context for Metabolic Disease Atherosclerosis.

作者信息

Marín de Evsikova Caralina, Raplee Isaac D, Lockhart John, Jaimes Gilberto, Evsikov Alexei V

机构信息

Department of Molecular Medicine, Morsani College of Medicine, University of South Florida, Tampa, FL 33612, USA.

Epigenetics & Functional Genomics Laboratories, Department of Research and Development, Bay Pines Veteran Administration Healthcare System, Bay Pines, FL 33744, USA.

出版信息

J Pers Med. 2019 Apr 29;9(2):21. doi: 10.3390/jpm9020021.

Abstract

As one of the most widespread metabolic diseases, atherosclerosis affects nearly everyone as they age; arteries gradually narrow from plaque accumulation over time reducing oxygenated blood flow to central and periphery causing heart disease, stroke, kidney problems, and even pulmonary disease. Personalized medicine promises to bring treatments based on individual genome sequencing that precisely target the molecular pathways underlying atherosclerosis and its symptoms, but to date only a few genotypes have been identified. A promising alternative to this genetic approach is the identification of pathways altered in atherosclerosis by transcriptome analysis of atherosclerotic tissues to target specific aspects of disease. Transcriptomics is a potentially useful tool for both diagnostics and discovery science, exposing novel cellular and molecular mechanisms in clinical and translational models, and depending on experimental design to identify and test novel therapeutics. The cost and time required for transcriptome analysis has been greatly reduced by the development of next generation sequencing. The goal of this resource article is to provide background and a guide to appropriate technologies and downstream analyses in transcriptomics experiments generating ever-increasing amounts of gene expression data.

摘要

作为最普遍的代谢性疾病之一,动脉粥样硬化几乎会随着每个人年龄的增长而影响他们;随着时间的推移,动脉会因斑块堆积而逐渐变窄,减少向中枢和外周输送的含氧血流,从而导致心脏病、中风、肾脏问题,甚至肺部疾病。个性化医疗有望带来基于个体基因组测序的治疗方法,精确靶向动脉粥样硬化及其症状背后的分子途径,但迄今为止,仅鉴定出少数几种基因型。这种基因方法的一种有前景的替代方法是通过对动脉粥样硬化组织进行转录组分析来鉴定动脉粥样硬化中改变的途径,以针对疾病的特定方面。转录组学对于诊断和发现科学而言是一种潜在有用的工具,它能在临床和转化模型中揭示新的细胞和分子机制,并依据实验设计来识别和测试新的治疗方法。下一代测序技术的发展极大地降低了转录组分析所需的成本和时间。这篇资源文章的目的是提供背景信息,并指导在转录组学实验中采用适当的技术和进行下游分析,这些实验会产生越来越多的基因表达数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37d1/6617151/eaa8b9dcb2ca/jpm-09-00021-g001.jpg

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