Pollard H B, Eidelman O, Jacobson K A, Srivastava M
Department of Anatomy, Physiology, and Genetics, and Institute for Molecular Medicine, USUHS School of Medicine, Bethesda, MD 20814, USA.
Mol Interv. 2001 Apr;1(1):54-63.
Pharmacogenomics is becoming a frontline instrument of drug discovery, where the drug-dependent patterns of global gene expression are employed as biologically relevant end points. In the case of cystic fibrosis (CF), cells and tissues from CF patients provide the starting points of genomic analysis. The end points for drug discovery are proposed to reside in gene expression patterns of CF cells that have been corrected by gene therapy. A case is made here that successful drug therapy and gene therapy should, hypothetically, converge at a common end point. In response to a virtual tidal wave of genomic data, bioinformatics algorithms are needed to identify those genes that truly reveal drug efficacy. As examples, we describe the hierarchical clustering, GRASP, and GENESAVER algorithms, particularly within a hypothesis-driven context that focuses on data for a CF candidate drug. Pharmacogenomic approaches to CF, and other similar diseases, may eventually give us the opportunity to create drugs that work in a patient- or mutation-specific manner.
药物基因组学正成为药物研发的前沿工具,其中全球基因表达的药物依赖性模式被用作生物学相关的终点。在囊性纤维化(CF)的情况下,CF患者的细胞和组织提供了基因组分析的起点。药物研发的终点被认为存在于经基因治疗纠正的CF细胞的基因表达模式中。本文提出一个观点,即假设成功的药物治疗和基因治疗应在一个共同的终点上汇聚。为应对基因组数据的虚拟浪潮,需要生物信息学算法来识别那些真正揭示药物疗效的基因。作为例子,我们描述了层次聚类、GRASP和GENESAVER算法,特别是在以CF候选药物数据为重点的假设驱动背景下。针对CF和其他类似疾病的药物基因组学方法最终可能使我们有机会创造出以患者或突变特异性方式起作用的药物。