Direct detection of carcinoembryonic antigen autoantibodies in clinical human serum samples using a surface plasmon resonance sensor

被引:62
作者
Ladd, Jon [1 ]
Lu, Hailing [2 ]
Taylor, Allen D. [1 ]
Goodell, Vivian [2 ]
Disis, Mary L. [2 ]
Jiang, Shaoyi [1 ]
机构
[1] Univ Washington, Dept Chem Engn, Seattle, WA 98195 USA
[2] Univ Washington, Div Oncol, Tumor Vaccine Grp, Seattle, WA 98195 USA
关键词
Carcinoembryonic antigen; CEA; Surface plasmon resonance; SPR; Autoantibody; Cancer; Biomarker; SELF-ASSEMBLED MONOLAYERS; PROTEIN IMMOBILIZATION; ANTIBODY ARRAYS; PROSTATE-CANCER; OVARIAN-CANCER; BREAST-CANCER; CELLS; MICROARRAYS; EXPRESSION; BIOSENSORS;
D O I
10.1016/j.colsurfb.2008.11.032
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The ability to detect biomarkers in human serum is important for cancer diagnostics. The work presented focuses on the establishment of a surface plasmon resonance (SPR) biosensor as a means for detecting varying levels of autoantibody biomarkers in human serum samples. Carcinoembryonic antigen (CEA) is a biomarker that is present in human serum. It is thought that CEA levels become elevated in patients with colon and ovarian cancer, causing a corresponding increase in the autoantibody level in human serum. Detection of this CEA autoantibody increase could be used to diagnose cancer in patients. Using a SPR biosensor, human serum samples were screened directly for CEA antibody levels. Results using a sandwich assay with a SPR sensor demonstrated the same linear trend as seen from an established enzyme-linked immunosorbent assay (ELISA) method. Serum samples from five healthy individuals were used to establish a threshold value for differentiating a cancerous serum sample from a negative sample with a 95% confidence. Three serum samples from cancer patients with positive CEA antibody levels as evaluated by ELISA were used to test the criterion. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 6
页数:6
相关论文
共 41 条
[1]   Drug-induced increase of carcinoembryonic antigen expression in cancer cells [J].
Aquino, A ;
Formica, V ;
Prete, SP ;
Correale, PP ;
Massara, MC ;
Turriziani, M ;
De Vecchis, L ;
Bonmassar, E .
PHARMACOLOGICAL RESEARCH, 2004, 49 (05) :383-396
[2]   DNA directed protein immobilization on mixed ssDNA/oligo(ethylene glycol) self-assembled monolayers for sensitive biosensors [J].
Boozer, C ;
Ladd, J ;
Chen, SF ;
Yu, Q ;
Homola, J ;
Jiang, SY .
ANALYTICAL CHEMISTRY, 2004, 76 (23) :6967-6972
[3]   Cancer immunomics: Using autoantibody signatures in the early detection of prostate cancer [J].
Bradford, Timothy J. ;
Wang, Xiaoju ;
Chinnaiyan, Arul M. .
UROLOGIC ONCOLOGY-SEMINARS AND ORIGINAL INVESTIGATIONS, 2006, 24 (03) :237-242
[4]   Protein and antibody arrays and their medical applications [J].
Cahill, DJ .
JOURNAL OF IMMUNOLOGICAL METHODS, 2001, 250 (1-2) :81-91
[5]  
CHAPMAN C, 2007, ANN ONCOLOGY
[6]   Clinically related protein-peptide interactions monitored in real time on novel peptide chips by surface plasmon resonance imaging [J].
Cherif, B ;
Roget, A ;
Villiers, CL ;
Calemczuk, R ;
Leroy, V ;
Marche, PN ;
Livache, T ;
Villiers, MB .
CLINICAL CHEMISTRY, 2006, 52 (02) :255-262
[7]   Antibody arrays for high-throughput screening of antibody-antigen interactions [J].
de Wildt, RMT ;
Mundy, CR ;
Gorick, BD ;
Tomlinson, IM .
NATURE BIOTECHNOLOGY, 2000, 18 (09) :989-994
[8]   High-titer HER-2/neu protein-specific antibody can be detected in patients with early-stage breast cancer [J].
Disis, ML ;
Pupa, SM ;
Gralow, JR ;
Dittadi, R ;
Menard, S ;
Cheever, MA .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (11) :3363-3367
[9]  
DISIS ML, 1994, CANCER RES, V54, P16
[10]   Multichannel surface plasmon resonance biosensor with wavelength division multiplexing [J].
Dostálek, J ;
Vaisocherová, H ;
Homola, J .
SENSORS AND ACTUATORS B-CHEMICAL, 2005, 108 (1-2) :758-764