Dietary copper and dimethylhydrazine affect protein kinase C isozyme protein and mRNA expression and the formation of aberrant crypts in colon of rats

被引:11
作者
Davis, CD [1 ]
Johnson, WT [1 ]
机构
[1] ARS, USDA, Grand Forks Human Nutr Res Ctr, Grand Forks, ND 58202 USA
关键词
D O I
10.1002/biof.5520150102
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Low dietary copper has been shown to decrease the expression of various protein kinase C (PKC) isozymes and increase the risk of colon cancer development in experimental animals. The purpose of this study was to investigate the relationship between dietary copper and carcinogen administration on PKC isozyme accumulation and aberrant crypt foci (ACF) formation in rats fed 0.9 and 7.7 mug Cu/g diet. After 24 and 31 d on the diets, the rats were injected with either dimethylhydrazine (DMH) (25 mg/kg i.p.) or saline and killed at two time points (2 wk and 8 wk after DMH). Rats fed low dietary copper bad significantly lower (p < 0.0001) hematocrits, hemoglobin, ceruloplasmin activity and plasma and liver copper concentrations than rats fed adequate dietary copper. Ingestion of low dietary copper significantly (p < 0.005) increased the formation of DMH-induced ACF (116.8 vs 59.6). Low dietary copper significantly (p < 0.05) decreased the concentration of PKC <alpha>, delta, and zeta in the colon at 2 wk but not at 8 wk. Thus, changes in PKC isoform protein concentration may be related to increased susceptibility of copper-deficient animals to colon cancer.
引用
收藏
页码:11 / 26
页数:16
相关论文
共 54 条
[1]  
*AM CANC SOC, 1997, CANC FACTS FIG
[2]  
BAUM CL, 1990, CANCER RES, V50, P3915
[3]   ROLE OF ABERRANT CRYPT FOCI IN UNDERSTANDING THE PATHOGENESIS OF COLON-CANCER [J].
BIRD, RP .
CANCER LETTERS, 1995, 93 (01) :55-71
[4]  
Blobe GC, 1996, CANCER SURV, V27, P213
[5]  
BLUMBERG PM, 1988, CANCER RES, V48, P1
[6]   PREMALIGNANT ALTERATIONS IN THE LIPID-COMPOSITION AND FLUIDITY OF COLONIC BRUSH-BORDER MEMBRANES OF RATS ADMINISTERED 1,2 DIMETHYLHYDRAZINE [J].
BRASITUS, TA ;
DUDEJA, PK ;
DAHIYA, R .
JOURNAL OF CLINICAL INVESTIGATION, 1986, 77 (03) :831-840
[7]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[8]  
CRAVEN PA, 1992, CANCER RES, V52, P2216
[9]  
CRAVEN PA, 1987, CANCER RES, V47, P3434
[10]  
DAVIDSON LA, 1995, CANCER EPIDEM BIOMAR, V4, P643