Application of mass spectrometry to the discovery of biomarkers for detection of prostate cancer

被引:26
作者
Semmes, O. John [1 ]
Malik, Gunjan [1 ]
Ward, Mike [1 ]
机构
[1] Eastern Virginia Med Sch, Ctr Biomed Prote, Virginia Prostate Ctr, Norfolk, VA 23507 USA
关键词
proteomics; prostate cancer; profiling; proteins; peptides; biomarkers;
D O I
10.1002/jcb.20855
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
There has been an impressive emergence of mass spectrometry based technologies applied toward the study of proteins. Equally notable is the rapid adaptation of these technologies to biomedical approaches in the realm of clinical proteomics. Concerted efforts toward the elucidation of the proteomes of organ sites or specific disease state are proliferating and from these efforts come the promise of better diagnostics/prognostics and therapeutic intervention. Prostate cancer has been a focus of many such Studies with the Promise of improved care to patients via biomarkers derived from these proteomic approaches. The newer technologies provide higher analytical capabilities, employ automated liquid handling systems, fractionation techniques and bioinformatics tools for greater sensitivity and resolving power, more robust and higher throughput sample processing, and greater confidence in analytical results. In this prospects, we summarize the proteomic technologies applied to date in Prostate cancer, along with their respective advantages and disadvantages. The development of newer proteomic strategies for use in future applications is also discussed. J. Cell. Biochem. 98: 496-503, 2006. (c) 2006 Wiley-Liss, Inc.
引用
收藏
页码:496 / 503
页数:8
相关论文
共 65 条
[1]  
Adam BL, 2002, CANCER RES, V62, P3609
[2]   Proteomic analysis of human prostate cancer [J].
Ahram, M ;
Best, CJM ;
Flaig, MJ ;
Gillespie, JW ;
Leiva, IM ;
Chuaqui, RF ;
Zhou, G ;
Shu, HJ ;
Duray, PH ;
Linehan, WM ;
Raffeld, M ;
Ornstein, DK ;
Zhao, YM ;
Petricoin, EF ;
Emmert-Buck, MR .
MOLECULAR CARCINOGENESIS, 2002, 33 (01) :9-15
[3]   Diagnostic potential of serum proteomic patterns in prostate cancer [J].
Bañez, LL ;
Prasanna, P ;
Sun, L ;
Ali, A ;
Zou, ZQ ;
Adam, BL ;
McLeod, DG ;
Moul, JW ;
Srivastava, S .
JOURNAL OF UROLOGY, 2003, 170 (02) :442-446
[4]   The androgen receptor is significantly associated with vascular endothelial growth factor and hypoxia sensing via hypoxia-inducible factors HIF-1a, HIF-2a, and the prolyl hydroxylases in human prostate cancer [J].
Boddy, JL ;
Fox, SB ;
Han, C ;
Campo, L ;
Turley, H ;
Kanga, S ;
Malone, PR ;
Harris, AL .
CLINICAL CANCER RESEARCH, 2005, 11 (21) :7658-7663
[5]   Integrated microfluidic system enabling (bio)chemical reactions with on-line MALDI-TOF mass spectrometry [J].
Brivio, M ;
Fokkens, RH ;
Verboom, W ;
Reinhoudt, DN ;
Tas, NR ;
Goedbloed, M ;
van den Berg, A .
ANALYTICAL CHEMISTRY, 2002, 74 (16) :3972-3976
[6]  
Cazares LH, 2002, CLIN CANCER RES, V8, P2541
[7]   Combined top-down and bottom-up mass spectrometric approach to characterization of biomarkers for renal disease [J].
Chalmers, MJ ;
Mackay, CL ;
Hendrickson, CL ;
Wittke, S ;
Walden, M ;
Mischak, H ;
Fliser, D ;
Just, I ;
Marshall, AG .
ANALYTICAL CHEMISTRY, 2005, 77 (22) :7163-7171
[8]   Androgens induce CD-9 in human prostate tissue [J].
Chuan, Y ;
Pang, ST ;
Bergh, A ;
Norstedt, G ;
Pousette, Å .
INTERNATIONAL JOURNAL OF ANDROLOGY, 2005, 28 (05) :291-296
[9]  
Conrads Thomas P, 2004, Mol Diagn, V8, P77, DOI 10.2165/00066982-200408020-00001
[10]   Search for cancer markers from endometrial tissues using differentially labeled tags iTRAQ and clCAT with multidimensional liquid chromatography and tandem mass spectrometry [J].
DeSouza, L ;
Diehl, G ;
Rodrigues, MJ ;
Guo, JZ ;
Romaschin, AD ;
Colgan, TJ ;
Siu, KWM .
JOURNAL OF PROTEOME RESEARCH, 2005, 4 (02) :377-386