Proteomic analysis of formalin-fixed prostate cancer tissue

被引:208
作者
Hood, BL
Darfler, MM
Guiel, TG
Furusato, B
Lucas, DA
Ringeisen, BR
Sesterhenn, IA
Conrads, TP
Veenstra, TD
Krizman, DB
机构
[1] Express Pathol Inc, Gaithersburg, MD 20877 USA
[2] NCI, Lab Proteom & Anal Technol, SAIC Frederick Inc, Frederick, MD 21702 USA
[3] Armed Forces Inst Pathol, Dept Genitourinary Pathol, Washington, DC 20306 USA
[4] USN, Res Lab, Washington, DC 20375 USA
关键词
D O I
10.1074/mcp.M500102-MCP200
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Proteomic analysis of formalin-fixed paraffin-embedded (FFPE) tissue would enable retrospective biomarker investigations of this vast archive of pathologically characterized clinical samples that exist worldwide. These FFPE tissues are, however, refractory to proteomic investigations utilizing many state of the art methodologies largely due to the high level of covalently cross-linked proteins arising from formalin fixation. A novel tissue microdissection technique has been developed and combined with a method to extract soluble peptides directly from FFPE tissue for mass spectral analysis of prostate cancer (PCa) and benign prostate hyperplasia (BPH). Hundreds of proteins from PCa and BPH tissue were identified, including several known PCa markers such as prostate-specific antigen, prostatic acid phosphatase, and macrophage inhibitory cytokine-1. Quantitative proteomic profiling utilizing stable isotope labeling confirmed similar expression levels of prostate-specific antigen and prostatic acid phosphatase in BPH and PCa cells, whereas the expression of macrophage inhibitory cytokine-1 was found to be greater in PCa as compared with BPH cells.
引用
收藏
页码:1741 / 1753
页数:13
相关论文
共 41 条
[1]   Evaluation of ethanol-fixed, paraffin-embedded tissues for proteomic applications [J].
Ahram, M ;
Flaig, MJ ;
Gillespie, JW ;
Duray, PH ;
Linehan, WM ;
Ornstein, DK ;
Niu, SL ;
Zhao, YM ;
Petricoin, EF ;
Emmert-Buck, MR .
PROTEOMICS, 2003, 3 (04) :413-421
[2]   Proteome-wide analysis of head and neck squamous cell carcinomas using laser-capture microdissection and tandem mass spectrometry [J].
Baker, H ;
Patel, V ;
Molinolo, AA ;
Shillitoe, EJ ;
Ensley, JF ;
Yoo, GH ;
Meneses-García, A ;
Myers, JN ;
El-Naggar, AK ;
Gutkind, JS ;
Hancock, WS .
ORAL ONCOLOGY, 2005, 41 (02) :183-199
[3]   Exploiting the complementary nature of LC/MALDI/MS/MS and LC/ESI/MS/MS for increased proteome coverage [J].
Bodnar, WM ;
Blackburn, RK ;
Krise, JM ;
Moseley, MA .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 2003, 14 (09) :971-979
[4]   Expression of a novel member of the TGF-β superfamily, growth differentiation factor-15/macrophage-inhibiting cytokine-1 (GDF-15/MIC-1) in adult rat tissues [J].
Böttner, M ;
Suter-Crazzolara, C ;
Schober, A ;
Unsicker, K .
CELL AND TISSUE RESEARCH, 1999, 297 (01) :103-110
[5]   Release and analysis of polypeptides and glycopolypeptides from formalin-fixed, paraffin wax-embedded tissue [J].
Brooks, SA ;
Dwek, MV ;
Leathem, AJ .
HISTOCHEMICAL JOURNAL, 1998, 30 (08) :609-615
[6]   Assessing protein patterns in disease using imaging mass spectrometry [J].
Chaurand, P ;
Schwartz, SA ;
Caprioli, RM .
JOURNAL OF PROTEOME RESEARCH, 2004, 3 (02) :245-252
[7]   Protein profiling of microdissected prostate tissue links growth differentiation factor 15 to prostate carcinogenesis [J].
Cheung, PK ;
Woolcock, B ;
Adomat, H ;
Sutcliffe, M ;
Bainbridge, TC ;
Jones, EC ;
Webber, D ;
Kinahan, T ;
Sadar, M ;
Gleave, ME ;
Vielkind, J .
CANCER RESEARCH, 2004, 64 (17) :5929-5933
[8]   Laser microdissection and gene expression analysis on formaldehyde-fixed archival tissue [J].
Cohen, CD ;
Gröne, HJ ;
Gröne, EF ;
Nelson, PJ ;
Schlöndorff, D ;
Kretzler, M .
KIDNEY INTERNATIONAL, 2002, 61 (01) :125-132
[9]  
DeRisi J, 1996, NAT GENET, V14, P457
[10]   Laser capture microdissection [J].
EmmertBuck, MR ;
Bonner, RF ;
Smith, PD ;
Chuaqui, RF ;
Zhuang, ZP ;
Goldstein, SR ;
Weiss, RA ;
Liotta, LA .
SCIENCE, 1996, 274 (5289) :998-1001