Specific MALDI imaging and profiling for biomarker hunting and validation: Fragment of the 11S proteasome activator complex, reg alpha fragment, is a new potential ovary cancer biomarker

被引:150
作者
Lemaire, Remi
Menguellet, Sonia Ait
Stauber, Jonathan
Marchaudon, Valerie.
Lucot, Jean-Philippe
Collinet, Pierre
Farine, Marie-Odile
Vinatier, Denis
Day, Robert
Ducoroy, Patrick
Salzet, Michel [1 ]
Fournier, Isabelle
机构
[1] Univ Sci & Technol Lille, MALDI Imaging Team, FRE CNRS 2933, Lab Neuroimmunol Annelides, F-59650 Villeneuve Dascq, France
[2] CHRU Lille, Hop Jeanne De Flandre, Clin Gynecol, F-59000 Lille, France
[3] Hop Calmette CHRU, Serv Anat & Cytol Pathol, F-59037 Lille, France
[4] Univ Sherbrooke, Fac Med, Dept Pharmacol, Sherbrooke, PQ J1H 5N4, Canada
[5] IFR 100 Sante STIC, Plateforme Proteom, F-21000 Dijon, France
关键词
MALDI direct analysis; MALDI imaging; Ovarian cancer; biomarker hunting; biomarker validation; Proteasome; 11S;
D O I
10.1021/pr0702722
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
MALDI imaging mass spectrometry represents a new analytical tool to directly provide the spatial distribution and relative abundance of proteins in tissue. Twenty-five ovary carcinomas (stages III and IV) and 23 benign ovaries were directly analyzed using MALDI-TOF MS. The biomarker with the major prevalence (80%) has been fully identified using MALDI MS and nanoESI MS and MS/MS after separation by RP-HPLC and trypsin enzymatic digestion. This marker with an m/z of 9744 corresponds to 84 amino acid residues from the 11S proteasome activator complex, named PA28 or Reg-alpha. Validation of this marker has been performed using MALDI imaging, classical immunocytochemistry with an antibody raised against the C-terminal part of the protein, specific MALDI imaging, and Western blot analysis. The validation, using immunocytochemistry, confirmed the epithelial localization of this fragment with nucleus localization in benign epithelial cells and a cytoplasmic localization in carcinoma cells. This indicates that this antibody could be used to discriminate the borderline tumor cases. At this point, a multicentric study needs to be conducted in order to clearly establish the potential of this biomarker. Taken together these studies reflect that direct tissue analysis and specific MALDI imaging strategies facilitate biomarker hunting and validation which can be named pathological proteomics.
引用
收藏
页码:4127 / 4134
页数:8
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