Cancer immunomics - From serological Proteome analysis to multiple affinity protein profiling

被引:31
作者
Hardouin, Julie [1 ]
Lasserre, Jean-Paul [1 ]
Sylvius, Loik [1 ]
Joubert-Caron, Raymonde [1 ]
Caron, Michel [1 ]
机构
[1] Univ Paris 13, UFR SMBH Leonard De Vinci, CNRS UMR BioMoCeti 7033, Prot Biochem & Proteom Lab, F-93017 Bobigny, France
来源
AUTOIMMUNITY, PT C: THE MOSAIC OF AUTOIMMUNITY | 2007年 / 1107卷
关键词
autoantibodies; autoantibody; autoantibody signature; antoantigen; biomarker; cancer immunomics; mass spectrometry; proteome; proteomics; serological proteome analysis;
D O I
10.1196/annals.1381.024
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cancer remains one of the leading causes of death worldwide. Thus, to identify any useful biomarkers is still a need. We performed "cancer immunomics" to identify autoantibody signatures produced in response to the presence of either breast or colorectal cancer. SERo-logical proteome analysis (SERPA) was performed by two-dimensional (2-D) electrophoresis separation, immunoblotting, image analysis, and mass spectrometry. Alternatively, to identify the antigens recognized by the autoantibodies of cancer patients, we developed an approach combining 2-D immunoaffinity chromatography, enzymatic digestion of the isolated antigens, nano flow separation of the resulting peptides, and identification: MAPPing (multiple affinity protein profiling). By these approaches we identified both proteins recognized by autoantibodies independently of a cancer status, and a limited number of proteins reacting preferentially with cancer sera.
引用
收藏
页码:223 / 230
页数:8
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