Tissue microarrays: bridging the gap between research and the clinic

被引:50
作者
Braunschweig, T
Chung, JY
Hewitt, SM [1 ]
机构
[1] NCI, Tissue Array Res Program, Pathol Lab, Ctr Canc Res,NIH, Bethesda, MD 20892 USA
[2] Inje Univ, Coll Med, PharmacoGenom Res Ctr, Pusan, South Korea
[3] Inje Univ, Coll Med, Mol Cell Physiol Res Grp, Pusan 614735, South Korea
关键词
cell line; clinical trials; high throughput; histology methodologies; pathology; proteomics; tissue microarray; TMA; translational medicine; xenograft;
D O I
10.1586/14789450.2.3.325
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Tissue microarrays are a high-throughput method for the Investigation of biomarkers in multiple tissue specimens at once. This technique allows for the analysis of up to 500 tissue samples in a single experiment using immunohistochemistry and in situ hybridization. Recently, cell lines and xenografts have been reduced to a tissue microarray format and are being applied to preclinical drug development. In clinical research, tissue microarrays are applied at multiple levels: comprehensive analysis of samples in the context of a clinical trial or across a population. Tissue microarrays play a central role in translational research, facilitating the discovery of molecules that have potential roles in the diagnosis, prognosis and prediction of response to therapy.
引用
收藏
页码:325 / 336
页数:12
相关论文
共 81 条
[1]   Distinct types of diffuse large B-cell lymphoma identified by gene expression profiling [J].
Alizadeh, AA ;
Eisen, MB ;
Davis, RE ;
Ma, C ;
Lossos, IS ;
Rosenwald, A ;
Boldrick, JG ;
Sabet, H ;
Tran, T ;
Yu, X ;
Powell, JI ;
Yang, LM ;
Marti, GE ;
Moore, T ;
Hudson, J ;
Lu, LS ;
Lewis, DB ;
Tibshirani, R ;
Sherlock, G ;
Chan, WC ;
Greiner, TC ;
Weisenburger, DD ;
Armitage, JO ;
Warnke, R ;
Levy, R ;
Wilson, W ;
Grever, MR ;
Byrd, JC ;
Botstein, D ;
Brown, PO ;
Staudt, LM .
NATURE, 2000, 403 (6769) :503-511
[2]   Gene expression analysis by real-time reverse transcription polymerase chain reaction:: influence of tissue handling [J].
Almeida, A ;
Thiery, JP ;
Magdelénat, H ;
Radvanyi, F .
ANALYTICAL BIOCHEMISTRY, 2004, 328 (02) :101-108
[3]   Progression in cutaneous malignant melanoma is associated with distinct expression profiles -: A tissue microarray-based study [J].
Alonso, SR ;
Ortiz, P ;
Pollán, M ;
Pérez-Gómez, B ;
Sánchez, L ;
Acuña, MJ ;
Pajares, R ;
Martínez-Tello, FJ ;
Hortelano, CM ;
Piris, MA ;
Rodríguez-Peralto, JL .
AMERICAN JOURNAL OF PATHOLOGY, 2004, 164 (01) :193-203
[4]  
ANDERSON BD, 2004, J CLIN ONCOL, V22, P4794
[5]  
BATTIFORA H, 1990, LAB INVEST, V63, P722
[6]  
BATTIFORA H, 1986, LAB INVEST, V55, P244
[7]   Web-based tissue microarray image data analysis: Initial validation testing through prostate cancer Gleason grading [J].
Bova, GS ;
Parmigiani, G ;
Epstein, JI ;
Wheeler, T ;
Mucci, NR ;
Rubin, MA .
HUMAN PATHOLOGY, 2001, 32 (04) :417-427
[8]   Differential expression of peroxisome proliferator-activated receptor-α, -β, and -γ during rat embryonic development [J].
Braissant, O ;
Wahli, W .
ENDOCRINOLOGY, 1998, 139 (06) :2748-2754
[9]   X-chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2-/+ mouse brain [J].
Braunschweig, D ;
Simcox, T ;
Samaco, RC ;
LaSalle, JM .
HUMAN MOLECULAR GENETICS, 2004, 13 (12) :1275-1286
[10]  
Braunschweig T, 2004, COMB CHEM HIGH T SCR, V7, P575