Reverse-phase protein microarrays: application to biomarker discovery and translational medicine

被引:58
作者
VanMeter, Amy
Signore, Michele
Pierobon, Mariaelena
Espina, Virginia
Liotta, Lance A.
Petricoin, Emanuel F., III
机构
[1] George Mason Univ, Ctr Applied Proteom & Mol Med, Manassas, VA 20110 USA
[2] George Mason Univ, Ctr Applied Proteom Mol Med, Manassas, VA 20110 USA
[3] Inst Super Sanita, Rome, Italy
[4] Univ Padua, Dept Oncol & Surg Sevices, Clin Chirurg II, Padua, Italy
关键词
biomarker; individualized theraphy; microarray; phosphoprotein; protein; reverse-phase protein microarray; translational medicine;
D O I
10.1586/14737159.7.5.625
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Mapping of protein signaling networks within tumors can identify new targets for therapy and provide a means to stratify patients for individualized therapy. Kinases are important drug targets, as such kinase network information could become the basis for development of therapeutic strategies for improving treatment outcome. An urgent clinical goal is to identify functionally important molecular networks associated with subpopulations of patients that may not respond to conventional combination chemotherapy. Reverse-phase protein microarrays are a technology platform designed for quantitative, multiplexed analysis of specific phosphorylated, cleaved, or total (phosphorylated and nonphosphorylated) forms of cellular proteins from a limited amount of sample. This class of microarray can be used to interrogate cellular samples, serum or body fluids. This review focuses on the application of reverse-phase protein microarrays for translational research and therapeutic drug target discovery.
引用
收藏
页码:625 / 633
页数:9
相关论文
共 64 条
[1]  
AOKI H, 2007, FASEB J
[2]   Quantitative protein analysis from formalin-fixed tissues:: implications for translational clinical research and nanoscale molecular diagnosis [J].
Becker, K-F ;
Schott, C. ;
Hipp, S. ;
Metzger, V. ;
Porschewski, P. ;
Beck, R. ;
Naehrig, J. ;
Becker, I. ;
Hoefler, H. .
JOURNAL OF PATHOLOGY, 2007, 211 (03) :370-378
[3]   Kinase substrate protein microarray analysis of human colon cancer and hepatic metastasis [J].
Belluco, C ;
Mammano, E ;
Petricoin, E ;
Prevedello, L ;
Calvert, V ;
Liotta, L ;
Nitti, D ;
Lise, M .
CLINICA CHIMICA ACTA, 2005, 357 (02) :180-183
[4]   CATALYZED REPORTER DEPOSITION, A NOVEL METHOD OF SIGNAL AMPLIFICATION .2. APPLICATION TO MEMBRANE IMMUNOASSAYS [J].
BOBROW, MN ;
SHAUGHNESSY, KJ ;
LITT, GJ .
JOURNAL OF IMMUNOLOGICAL METHODS, 1991, 137 (01) :103-112
[5]   CATALYZED REPORTER DEPOSITION, A NOVEL METHOD OF SIGNAL AMPLIFICATION - APPLICATION TO IMMUNOASSAYS [J].
BOBROW, MN ;
HARRIS, TD ;
SHAUGHNESSY, KJ ;
LITT, GJ .
JOURNAL OF IMMUNOLOGICAL METHODS, 1989, 125 (1-2) :279-285
[6]   Cell sampling - Laser capture microdissection: Molecular analysis of tissue [J].
Bonner, RF ;
EmmertBuck, M ;
Cole, K ;
Pohida, T ;
Chuaqui, R ;
Goldstein, S ;
Liotta, LA .
SCIENCE, 1997, 278 (5342) :1481-&
[7]   Protein microarrays for multiplex analysis of signal transduction pathways [J].
Chan, SM ;
Ermann, J ;
Su, L ;
Fathman, CG ;
Utz, PJ .
NATURE MEDICINE, 2004, 10 (12) :1390-1396
[8]   Positional cloning of the gene for multiple endocrine neoplasia-type 1 [J].
Chandrasekharappa, SC ;
Guru, SC ;
Manickam, P ;
Olufemi, SE ;
Collins, FS ;
EmmertBuck, MR ;
Debelenko, LV ;
Zhuang, ZP ;
Lubensky, IA ;
Liotta, LA ;
Crabtree, JS ;
Wang, YP ;
Roe, BA ;
Weisemann, J ;
Boguski, MS ;
Agarwal, SK ;
Kester, MB ;
Kim, YS ;
Heppner, C ;
Dong, QH ;
Spiegel, AM ;
Burns, AL ;
Marx, SJ .
SCIENCE, 1997, 276 (5311) :404-407
[9]  
Charboneau Lu, 2002, Briefings in Functional Genomics & Proteomics, V1, P305, DOI 10.1093/bfgp/1.3.305
[10]   MULTI-ANALYTE IMMUNOASSAY [J].
EKINS, RP .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1989, 7 (02) :155-168