Identification of biomarkers associated with the development of hepatocellular carcinoma in CuZn superoxide dismutase deficient mice

被引:37
作者
Elchuri, Sailaja
Naeemuddin, Mohammed
Sharpe, Orr
Robinson, William H.
Huang, Ting-Ting
机构
[1] Stanford Univ, Dept Neurol & Neurol Sci, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Med, Div Rheumatol & Immunol, Stanford, CA 94305 USA
[3] VA Palo Alto Hlth Care Syst, GRECC, Palo Alto, CA USA
关键词
CuZn superoxide dismutase; GST mu1; hepatocellular carcinoma; regucalcin; senescence marker protein 30;
D O I
10.1002/pmic.200601011
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
To identify biomarkers associated with the development of hepatocellular carcinoma (HCC) in CuZn superoxide dismutase (CuZnSOD, Sod1) deficient mice, 2-DE followed by MS analysis was carried out with liver samples obtained from 18-month-old Sod1- / - and + / + mice. The intracellular Ca. binding protein, regucalcin (RGN), showed a divergent alteration in Sod 1 - / - samples. Whereas elevated RGN levels were observed in samples with no obvious neoplastic changes, marked reduction in RGN was observed in samples with fully developed HCC. GST mu1 (GSTM1), on the other hand, showed a significant increase only in the neoplastic regions obtained from Sod1-/- livers. No change in GSTM1 was observed in the surrounding normal tissues. Marked reduction was observed in two intracellular lipid transporters, fatty acid binding protein 1 (FABP1) and major urinary protein 11 and 8 (MUP 11&8), in Sod1-/- samples. Analysis of additional samples at 18-22 months of age showed a three-fold increase in enolase activities in Sod1-/- livers. Consistent with previous findings, carbonic anhydrase 3 (CAIII) levels were significantly reduced in Sod1-/- samples, and immunohistochemical analysis revealed that the reduction was not homogenous throughout the lobular structure in the liver.
引用
收藏
页码:2121 / 2129
页数:9
相关论文
共 44 条
[1]   Genes of glycolysis are ubiquitously overexpressed in 24 cancer classes [J].
Altenberg, B ;
Greulich, KO .
GENOMICS, 2004, 84 (06) :1014-1020
[2]   Effect of branched-chain fatty acid on lipid dynamics in mice lacking liver fatty acid binding protein gene [J].
Atshaves, BP ;
McIntosh, AL ;
Payne, HR ;
Mackie, J ;
Kier, AB ;
Schroeder, F .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2005, 288 (03) :C543-C558
[3]   Regulation of the gene encoding glutathione S-transferase M1 (GSTM1) by the Myb oncoprotein [J].
Bartley, PA ;
Keough, RA ;
Lutwyche, JK ;
Gonda, TJ .
ONCOGENE, 2003, 22 (48) :7570-7575
[4]   Improving large-scale proteomics by clustering of mass spectrometry data [J].
Beer, I ;
Barnea, E ;
Ziv, T ;
Admon, A .
PROTEOMICS, 2004, 4 (04) :950-960
[5]   Multiple roles of major urinary proteins in the house mouse, Mus domesticus [J].
Beynon, RJ ;
Hurst, JL .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2003, 31 :142-146
[6]   DECREASED ACTIVITY OF SCAVENGER ENZYMES IN HUMAN HEPATOCELLULAR-CARCINOMA, BUT NOT IN LIVER METASTASES [J].
CASARIL, M ;
CORSO, F ;
BASSI, A ;
CAPRA, F ;
GABRIELLI, GB ;
STANZIAL, AM ;
NICOLI, N ;
CORROCHER, R .
INTERNATIONAL JOURNAL OF CLINICAL & LABORATORY RESEARCH, 1994, 24 (02) :94-97
[7]   Loss of the Nrf2 transcription factor causes a marked reduction in constitutive and inducible expression of the glutathione S-transferase Gsta1, Gsta2, Gstm1, Gstm2, Gstm3 and Gstm4 genes in the livers of male and female mice [J].
Chanas, SA ;
Jiang, Q ;
McMahon, M ;
McWalter, GK ;
McLellan, LI ;
Elcombe, CR ;
Henderson, CJ ;
Wolf, CR ;
Moffat, GJ ;
Itoh, K ;
Yamamoto, M ;
Hayes, JD .
BIOCHEMICAL JOURNAL, 2002, 365 (02) :405-416
[8]   Detection of protein carbonyls in aging liver tissue: A fluorescence-based proteornic approach [J].
Chaudhuri, Asish R. ;
de Waal, Eric M. ;
Pierce, Anson ;
Van Remmen, Holly ;
Ward, Walter E. ;
Richardson, Arlan .
MECHANISMS OF AGEING AND DEVELOPMENT, 2006, 127 (11) :849-861
[9]   CuZnSOD deficiency leads to persistent and widespread oxidative damage and hepatocarcinogenesis later in life [J].
Elchuri, S ;
Oberley, TD ;
Qi, WB ;
Eisenstein, RS ;
Roberts, LJ ;
Van Remmen, H ;
Jepstein, CJ ;
Huang, TT .
ONCOGENE, 2005, 24 (03) :367-380
[10]   Senescence marker protein-30 (SMP30): Structure and biological function [J].
Fujita, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 254 (01) :1-4