Detection of tumor markers with ProteinChip® technology

被引:62
作者
Wiesner, A [1 ]
机构
[1] Ciphergen Biosyst GmbH, D-37085 Gottingen, Germany
关键词
SELDI; tumor marker; protein profiling; biomarker discovery; biomarker pattern; proteomics; ProteinChip((R)) Biomarker System; Expression Difference Mapping (TM) technique; Interaction Discovery Mapping (TM) platform;
D O I
10.2174/1389201043489675
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
The early diagnosis of cancer at a curable stage is crucial for the successful treatment of this disease. Most of the currently used tumor assays appear too late and rely on single biomarkers with high false-negative and/or false-positive rates. As an additional burden for the patient, the traditional assays often require biopsy material instead of less invasively taken samples like serum. With the hope for more reliable DNA- and RNA-based screening tools, the research activities of the past 20 years have focused on the genomic characteristics of cancer cells. But, up to now, the output from this strategy has been disappointingly low and the disillusionment is paired with a return to proteins as the real key players in all physiological and pathological processes. Meanwhile, comparative protein profiling is generally acknowledged as a promising way for the detection of specific and predictive protein patterns reflecting certain stages of cancer without dependency on single markers. To meet the new technological demands, the ProteinChip(R) Biomarker System was developed for the Expression Difference Mapping(TM) analysis of several hundreds of samples per day on a single, uncomplicated platform: with software support for the construction of multi-marker predictive models. The Interaction Discovery Mapping(TM) platform is introduced as the next methodical step for investigations about protein binding partners of possible importance in diagnosis and therapy. This review summarizes the current state in cancer diagnosis, provides an introduction into the ProteinChip technology, and gives an update on publications and research collaborations in SELDI-based tumor marker discovery.
引用
收藏
页码:45 / 67
页数:23
相关论文
共 127 条
[1]  
Adam BL, 2002, CANCER RES, V62, P3609
[2]  
ADAM BL, 2003, P AM ASSOC CANC RES, V44, pR6323
[3]   Insulin-like growth factor-binding protein 5 (IGFBP-5) interacts with a four and a half LIM protein 2 (FHL2) [J].
Amaar, YG ;
Thompson, GR ;
Linkhart, TA ;
Chen, ST ;
Baylink, DJ ;
Mohan, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (14) :12053-12060
[4]   Remarks on the structure and development of the have perfect [J].
Anderson, JM .
FOLIA LINGUISTICA HISTORICA, 1997, 18 (1-2) :3-23
[5]  
[Anonymous], 2003, CANC FACTS FIG
[6]   New technologies for the identification of markers for early detection of ovarian cancer [J].
Bandera, CA ;
Ye, B ;
Mok, SC .
CURRENT OPINION IN OBSTETRICS & GYNECOLOGY, 2003, 15 (01) :51-55
[7]   DNA affinity capture and protein profiling by SELDI-TOF mass spectrometry: effect of DNA methylation [J].
Bane, TK ;
LeBlanc, JF ;
Lee, TD ;
Riggs, AD .
NUCLEIC ACIDS RESEARCH, 2002, 30 (14) :e69
[8]   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
[9]   Protein profiling of complete mole and normal placenta using ProteinChip analysis on laser capture microdissected cells [J].
Batorfi, J ;
Ye, B ;
Mok, SC ;
Cseh, I ;
Berkowitz, RS ;
Fulop, V .
GYNECOLOGIC ONCOLOGY, 2003, 88 (03) :424-428
[10]   Generation of C-terminally truncated amyloid-β peptides is dependent on γ-secretase activity [J].
Beher, D ;
Wrigley, JDJ ;
Owens, AP ;
Shearman, MS .
JOURNAL OF NEUROCHEMISTRY, 2002, 82 (03) :563-575