Expression Genetics in Drug Therapy

药物治疗中的表达遗传学

• 批准号: 8497694
• 负责人: WOLFGANG SADEE
• 金额: $ 153.17万
• 依托单位: OHIO STATE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-07-16 至 2015-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8497694
• 关键词: Accounting; Address; Affect; Alleles; Amino Acid Sequence; Antipsychotic Agents; Area; Bioinformatics; Biological Assay; Biological Markers; Blood Cells; Blood Vessels; Brain; CETP gene; CYP2C9 gene; CYP2D6 gene; CYP3A4 gene; Candidate Disease Gene; Cardiovascular Diseases; Cardiovascular system; Central Nervous System Diseases; Child; Clinic; Clinical; Clinical Research; Clinical Trials; Clinical assessments; Complement; Complex; Coronary Arteriosclerosis; Coronary heart disease; DNA; DRD1 gene; DRD2 gene; Data; Databases; Dexamethasone; Disease; Disease Outcome; Dopamine; Dose; Drug Kinetics; Drug Receptors; Drug Targeting; ESR1 gene; Early Intervention; Elements; Environment; Enzymes; Epigenetic Process; Estrogen Receptors; Failure; Female; Future; Gene Expression Profiling; Gene Expression Regulation; Gene Targeting; Genes; Genetic; Genetic Markers; Genetic Polymorphism; Genetic Transcription; Genomics; Genotype; Glucocorticoid Receptor; Glucocorticoids; Goals; Heart; Heat-Shock Proteins 90; High Density Lipoproteins; Human; Individual; Kidney; Knowledge; Laboratories; Lead; Link; Liver; Low-Density Lipoproteins; Measures; Messenger RNA; Methods; MicroRNAs; Molecular; Molecular Genetics; Mutation; Myocardial Infarction; NR3C1 gene; Nephrotic Syndrome; Outcome; Oxidoreductase; Pathway interactions; Patients; Pattern; Penetrance; Peptide Sequence Determination; Pharmaceutical Preparations; Pharmacodynamics; Pharmacogenomics; Pharmacotherapy; Phase; Play; Prevention; Primer Extension; Process; Proteins; Psychotic Disorders; RNA Splicing; Receptor Signaling; Regulation; Reporter Genes; Research; Resistance; Resources; Role; Scanning; Schizophrenia; Science; Scientist; Series; Signal Pathway; Signal Transduction; Site; Source; Specificity; Steroid Receptors; Steroids; Surveys; TDO2 gene; Testing; Therapeutic; Tissues; Toxic effect; Transcript; Translating; Translation Process; Treatment outcome; Variant; Women' s Health; base; candidate identification; clinical phenotype; cohort; disease registry; dosage; drug metabolism; expectation; experience; first episode psychosis; fitness; functional genomics; gene interaction; genetic analysis; genetic selection; genetic variant; genome wide association study; genome-wide analysis; improved; in vivo; innovation; insight; lipid metabolism; mRNA Expression; next generation; programs; promoter; prospective; protein expression; receptor; repository; research clinical testing; response; statistics; transcription factor; treatment response

Understanding the genetic basis of disease and drug response has the potential to improve therapy and enable early intervention or prevention. However, the main genetic factors remain only partially understood, even while the number of candidate genes is rapidly growing, as a result of genome-wide association studies. Polymorphisms that alter protein sequence are readily detectable, but growing evidence indicates that regulatory polymorphisms are more prevalent, affecting mRNA expression, processing, and translation. Yet, regulatory variants are difficult to detect, and moreover, their functions depend on tissue context and environment, so that a majority remains hidden. The central goal of this proposal is a comprehensive discovery of regulatory polymorphisms in ~200 pharmacotherapeutic candidate genes, followed by molecular studies to understand the underlying mechanisms, and clinical evaluation in drug therapy - the first such systematic study in pharmacogenomics. We have developed a comprehensive approach to the discovery of regulatory polymorphisms, measuring allelic mRNA expression, processing, and translation in relevant human target tissues. This approach has already revealed unexpected and frequent regulatory variants in genes encoding drug metabolizing enzymes and receptors, gaining a powerful link between genotype of proven function and clinical outcomes (examples: DRD2, TPH2, ACE, VKORC1, CETP, and CYP3A4). These results support a critical role for regulatory polymorphisms in drug response. The main focus in this proposal is on drug metabolism genes and impact on pharmacokinetics-pharmacodynamics. In addition, building on other ongoing studies, the project includes genes encoding drug receptors/targets, with focus on CNS disorders (schizophrenia) and cardiovascular diseases (myocardial infarction, lipid metabolism), to be tested in association studies led by experienced clinical scientists. Driven by the motto 'from clinic to laboratory', new genetic studies have been initiated on estrogen and glucocorticoid receptors, the latter to be tested in glucocorticoid-resistant nephrotic syndrome in children. The long-term goal is to develop and validate genetic biomarker panels for optimizing personalized drug therapy.

了解疾病和药物反应的遗传基础有可能改进治疗，使早期干预或预防成为可能。然而，作为全基因组关联研究的结果，尽管候选基因的数量正在迅速增长，但主要的遗传因素仍然只有部分被了解。改变蛋白质序列的多态很容易被检测到，但越来越多的证据表明，调节性多态更普遍，影响mRNA的表达、加工和翻译。然而，调控变异很难被发现，而且它们的功能依赖于组织环境和环境，因此大多数都是隐藏的。这项建议的中心目标是全面发现约200个药物治疗候选基因的调节多态，随后进行分子研究以了解潜在的机制，并在药物治疗中进行临床评估-这是药物基因组学中第一个这样的系统研究。我们开发了一种全面的方法来发现调节性多态，测量相关人类靶组织中等位基因mRNA的表达、加工和翻译。这种方法已经在编码药物代谢酶和受体的基因中发现了意想不到的频繁调控变异，获得了已证实功能的基因型与临床结果之间的强大联系(例如：DRD2、TPH2、ACE、VKORC1、CETP和CYP3A4)。这些结果支持了调节性多态在药物反应中的关键作用。这项建议主要关注药物代谢基因及其对药代动力学-药效学的影响。此外，在其他正在进行的研究的基础上，该项目包括编码药物受体/靶标的基因，重点是中枢神经系统疾病(精神分裂症)和心血管疾病(心肌梗死、脂代谢)，将在经验丰富的临床科学家领导的关联研究中进行测试。在从临床到实验室的座右铭的推动下，关于雌激素和糖皮质激素受体的新的遗传学研究已经启动，后者将在儿童糖皮质激素抵抗型肾病综合征中进行测试。长期目标是开发和验证遗传生物标记物面板，以优化个性化药物治疗。