Table 5

Up-regulated genes in rats fed with SPI diet*

Category and Gene Name
Probe Set GB Accession No.
Fold Change
P value

Cell adhesion



     Collagen alpha1 type I
Z78279
2.49
0
     Secreted phosphoprotein 1
M14656
111.39
0.006
     Matrix metalloproteinase 13
M60616
24.34
0.002
     Regenerating islet
M62930
193.08
0.011
Defense/immunity protein



     Ig gamma-2a chain
L22654
115.17
0.001
     Ig gamma heavy chain
M28670
3.22
0
     Ig germline kappa-chain C-region
M18528
2.48
0.038
     Ig light-chain
U39609
2.63
0.021
     Fc-gamma
M32062
4.72
0.017
Detoxification



     Glutathione S-transferase 1
J03752
2.86
0
     Glutathione-S-transferase,alpha type2
K00136
2.56
0.009
     UDP glucuronosyltransferase
D38066
2.83
0.014
Metabolism



     Matrix metalloproteinase 7
L24374
3.63
0.02
     lysozyme
rc_AA892775
2.77
0
     Matrix metalloproteinase 12
X98517
11.8
0.013
     Mitochondrial carbamyl phosphate synthetase I
M12335
59.25
0.001
     Aldolase B, exon 9
X02291
8.7
0.01
     Aldolase B, exon 2
X02284
2.71
0.001
Signal transduction



     MHC class II antigen RT1.B-1 beta-chain
X56596
2.55
0.001
     CD3 gamma-chain
S79711
4.51
0.001
Ligand binding/carrier



     Intracellular calcium-binding protein
L18948
28.29
0.014
     Retinol binding protein II
M13949
5.11
0.001
     Apolipoprotein B
M27440
6.47
0.024
     Apolipoprotein A-I
J02597
2.49
0.004
     Iron ion transporter
AF008439
18.78
0.008
Stress response/apoptosis



     Heme oxygenase
J02722
9.66
0.002
     JE product
X17053
3.52
0.001
     Pancreatitis-associated protein
M98049
68.39
0.004
     Pancreatitis associated protein III
L20869
15.35
0
     Reg protein
E01983
30.25
0.001
Others



     Histamine N-tele-methyltransferase
S82579
6.17
0.04

*Changes in gene expression were determined by t-test (DMT), comparative analysis (MAS 5.0), and SAM (Stanford). Gene expression profiles from CAS animals were used as control. P value and fold-change are based on the DMT analysis; whereas final listed genes met all of the analytical criteria as described in the Methods.

Xiao et al. Molecular Cancer 2005 4:1   doi:10.1186/1476-4598-4-1