Potential protein markers for nutritional health effects on colorectal cancer in the mouse as revealed by proteomics analysis

被引:35
作者
Breikers, Githa
van Breda, Simone G. J.
Bouwman, Freek G.
van Herwijnen, Marcel H. M.
Renes, Johan
Mariman, Edwin C. M.
Kleinjans, Jos C. S.
van Delft, Joost H. M.
机构
[1] Maastricht Univ, Dept Hlth Risk Anal & Toxicol, NL-6200 MD Maastricht, Netherlands
[2] Maastricht Univ, Maastricht Prote Ctr, Dept Human Biol, Maastricht, Netherlands
关键词
colorectal cancer; MALDI-TOF mass spectrometry; two-dimensional gel electrophoresis; vegetables;
D O I
10.1002/pmic.200500067
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
It is suggested that colorectal cancer might be prevented by changes in diet, and vegetable consumption has been demonstrated to have a protective effect. Until now, little is known about the effects of vegetable consumption at the proteome level. Therefore, the effect of increased vegetable intake on the protein expression in the colonic mucosa of healthy mice was studied. Aim was to identify the proteins that are differentially expressed by increased vegetable consumption and to discriminate their possible role in the protection against colorectal cancer. Mice were fed four different vegetable diets, which was followed by analysis of total cellular protein from colonic mucosal cells by a combination of 2-DE and MS. We found 30 proteins that were differentially expressed in one or more diets as compared to the control diet. Six could be identified by MALDI-TOF MS: myosin regulatory light chain 2, carbonic anhydrase 1, high-mobility group protein 1, pancreatitis-associated protein 3, glyceraldehyde-3-phosphate dehydrogenase and ATP synthase oligomycin sensitivity conferral protein. Alterations in the levels of these proteins agree with a role in the protection against colon cancer. We conclude that these proteins are suitable markers for the health effect of food on cancer. The observed altered protein levels therefore provide support for the protective effects of vegetables against colorectal cancer.
引用
收藏
页码:2844 / 2852
页数:9
相关论文
共 63 条
[1]   REGULATION AND KINETICS OF THE ACTIN-MYOSIN-ATP INTERACTION [J].
ADELSTEIN, RS ;
EISENBERG, E .
ANNUAL REVIEW OF BIOCHEMISTRY, 1980, 49 :921-956
[2]  
BERTRAM JS, 1995, AM J CLIN NUTR, V62, P1327
[3]  
Bertram JS, 1999, NUTR REV, V57, P182, DOI 10.1111/j.1753-4887.1999.tb06941.x
[4]   Upwardly mobile proteins Workshop: The role of HMG proteins in chromatin structure, gene expression and neoplasia [J].
Bianchi, Marco E. ;
Beltrame, Monica .
EMBO REPORTS, 2000, 1 (02) :109-114
[5]   A combination of protein profiling and isotopomer analysis using matrix-assisted laser desorption/ionization-time of flight mass spectrometry reveals an active metabolism of the extracellular matrix of 3T3-L1 adipocytes [J].
Bouwman, F ;
Renes, J ;
Mariman, E .
PROTEOMICS, 2004, 4 (12) :3855-3863
[6]  
Chiang WL, 2002, CANCER LETT, V188, P199, DOI 10.1016/S0304-3835(02)00078-2
[7]   Inhibition of N-acetyltransferase activity and gene expression in human colon cancer cell lines by diallyl sulfide [J].
Chung, JG ;
Lu, HF ;
Yeh, CC ;
Cheng, KC ;
Lin, SS ;
Lee, JH .
FOOD AND CHEMICAL TOXICOLOGY, 2004, 42 (02) :195-202
[8]  
Cuezva JM, 2002, CANCER RES, V62, P6674
[9]  
CUMMINGS JH, 1978, LANCET, V1, P5, DOI 10.1016/S0140-6736(78)90357-4
[10]   SPECTRAL PROPERTIES OF FLUORESCENT DERIVATIVES OF THE OLIGOMYCIN SENSITIVITY CONFERRING PROTEIN AND ANALYSIS OF THEIR INTERACTION WITH THE F1 AND F0 SECTORS OF THE MITOCHONDRIAL ATPASE COMPLEX [J].
DUSZYNSKI, J ;
DUPUIS, A ;
LUX, B ;
VIGNAIS, PV .
BIOCHEMISTRY, 1988, 27 (17) :6288-6296