Therianos Stavros, Zhu Min, Pyun Eunice, Coleman Paul D
Center for Aging and Developmental Biology, University of Rochester Medical Center, Rochester, New York 14610, USA.
Am J Pathol. 2004 Mar;164(3):795-806. doi: 10.1016/S0002-9440(10)63168-9.
Effective approaches using array technologies are critical to understand the molecular bases of human diseases. The results obtained using such procedures require analysis and validation procedures that are still under development. In the context of Alzheimer's disease, in which the identification of molecular mechanisms of underlying pathologies is vital, we describe a robust assay that is the first real-time reverse transcriptase-polymerase chain reaction-based high-throughput approach that can simultaneously quantitate the expression of a large number of genes at the copy number level from a minute amount of starting material. Using this approach within the human brain, we were able to quantitate as many as 19 genes at a time with only one type of fluorescent probe. The number of genes included can be considerably increased. Examples of consistent changes in Alzheimer's disease within these 19 candidate genes included reductions in targets related to the dendritic and synaptic apparatus. These changes were specific to Alzheimer's disease when compared with Parkinson's disease cases. We also present comparison data with microarray analysis from the same brain region and the same patients. The high sensitivity and reproducibility of this technology coupled with appropriate multivariate analysis is proposed here to form a biotechnology platform that can be widely used for diagnostic purposes as well as basic research.
使用阵列技术的有效方法对于理解人类疾病的分子基础至关重要。使用此类程序获得的结果需要仍在开发中的分析和验证程序。在阿尔茨海默病的背景下,其中潜在病理分子机制的鉴定至关重要,我们描述了一种强大的检测方法,这是第一种基于实时逆转录聚合酶链反应的高通量方法,能够从微量起始材料中在拷贝数水平上同时定量大量基因的表达。在人类大脑中使用这种方法,我们能够仅用一种荧光探针一次定量多达19个基因。所包含的基因数量可以大幅增加。在这19个候选基因中,阿尔茨海默病中一致变化的例子包括与树突和突触装置相关靶点的减少。与帕金森病病例相比,这些变化是阿尔茨海默病特有的。我们还展示了来自同一脑区和相同患者的微阵列分析的比较数据。本文提出该技术的高灵敏度和可重复性以及适当的多变量分析,以形成一个可广泛用于诊断目的以及基础研究的生物技术平台。