Clinical Translation of Cell-Based Pharmacogenomic Discovery

被引:17
作者
Cox, N. J. [1 ]
Gamazon, E. R.
Wheeler, H. E.
Dolan, M. E. [1 ]
机构
[1] Univ Chicago, Dept Med, Comm Clin Pharmacol & Pharmacogenom, Chicago, IL 60637 USA
基金
美国国家卫生研究院;
关键词
EXPRESSION;
D O I
10.1038/clpt.2012.115
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The use of cell-based models has emerged as a promising means to discover and validate pharmacologic phenotype-genotype relationships. The availability of large-scale genome studies in both human and model systems is now allowing us an unprecedented opportunity to understand how well cell-based models identify clinically relevant genetic variants associated with drug response and toxicity. Here we review these studies and the emerging translational information.
引用
收藏
页码:425 / 427
页数:3
相关论文
共 4 条
[1]   Gene Expression in Skin and Lymphoblastoid Cells: Refined Statistical Method Reveals Extensive Overlap in cis-eQTL Signals [J].
Ding, Jun ;
Gudjonsson, Johann E. ;
Liang, Liming ;
Stuart, Philip E. ;
Li, Yun ;
Chen, Wei ;
Weichenthal, Michael ;
Ellinghaus, Eva ;
Franke, Andre ;
Cookson, William ;
Nair, Rajan P. ;
Elder, James T. ;
Abecasis, Goncalo R. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2010, 87 (06) :779-789
[2]   Genetic architecture of transcript-level variation in humans [J].
Duan, Shiwei ;
Huang, R. Stephanie ;
Zhang, Wei ;
Bleibel, Wasim K. ;
Roe, Cheryl A. ;
Clark, Tyson A. ;
Chen, Tina X. ;
Schweitzer, Anthony C. ;
Blume, John E. ;
Cox, Nancy J. ;
Dolan, M. Eileen .
AMERICAN JOURNAL OF HUMAN GENETICS, 2008, 82 (05) :1101-1113
[3]   Chemotherapeutic drug susceptibility associated SNPs are enriched in expression quantitative trait loci [J].
Gamazon, Eric R. ;
Huang, R. Stephanie ;
Cox, Nancy J. ;
Dolan, M. Eileen .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (20) :9287-9292
[4]  
Wheeler HE, 2012, PHARMACOGENOMICS, V13, P55, DOI [10.2217/PGS.11.121, 10.2217/pgs.11.121]