Tumor promotion by hydrogen peroxide in rat liver epithelial cells

被引:54
作者
Huang, RP [1 ]
Peng, A [1 ]
Hossain, MZ [1 ]
Fan, Y [1 ]
Jagdale, A [1 ]
Boynton, AL [1 ]
机构
[1] Northwest Hosp, Mol Med, Seattle, WA 98125 USA
关键词
D O I
10.1093/carcin/20.3.485
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Reactive oxygen species, including H2O2, play an important role in the tumor promotion process. Using an in vitro model of tumor promotion involving the rat liver epithelial oval cell line T51B, the tumor promoting activity of H2O2 in N-methyl-N '-nitro-N-nitrosoguanidine-initiated cells was studied. In this assay system, the promoting effect of H2O2 is evidenced by the formation of colonies in soft agar, appearance of foci in monolayer culture, disruption of gap junction communication (GJC) in foci areas and growth at higher saturation densities. H2O2 preferentially induced the expression of c-fos, c-jun, c-myc and egr-1, while JunB and JunD levels remained almost unchanged. H2O2 also induced hyperphosphorylation of Cx43 and disruption of GJC, The effects of H2O2 on tumor promotion, induction of immediate early (IE) genes and disruption of GJC are blocked by antioxidants, These results suggest that H2O2 acts as a tumor promoter in rat liver non-neoplastic epithelial cells and that the induction of IE genes and disruption of GJC are two possible targets of H2O2 during the tumor promotion process.
引用
收藏
页码:485 / 492
页数:8
相关论文
共 89 条
[1]   REDOX REGULATION OF FOS AND JUN DNA-BINDING ACTIVITY INVITRO [J].
ABATE, C ;
PATEL, L ;
RAUSCHER, FJ ;
CURRAN, T .
SCIENCE, 1990, 249 (4973) :1157-1161
[2]   Role of oxidative stress in the selective toxicity of dieldrin in the mouse liver [J].
Bachowski, S ;
Xu, Y ;
Stevenson, DE ;
Walborg, EF ;
Klaunig, JE .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1998, 150 (02) :301-309
[3]  
Bachowski S, 1997, ANN CLIN LAB SCI, V27, P196
[4]   INHIBITION OF CHRYSAROBIN SKIN TUMOR PROMOTION IN SENCAR MICE BY ANTIOXIDANTS [J].
BATTALORA, MS ;
KRUSZEWSKI, FH ;
DIGIOVANNI, J .
CARCINOGENESIS, 1993, 14 (12) :2507-2512
[5]   CYTOKERATIN 14 EXPRESSION IN RAT-LIVER CELLS IN CULTURE AND LOCALIZATION INVIVO [J].
BLOUIN, R ;
BLOUIN, MJ ;
ROYAL, I ;
GRENIER, A ;
ROOP, DR ;
LORANGER, A ;
MARCEAU, N .
DIFFERENTIATION, 1992, 52 (01) :45-54
[6]  
BOSTICK RM, 1993, CANCER RES, V53, P4230
[7]  
BRAUN L, 1989, CANCER RES, V49, P1554
[8]   The tumor promoter arsenite stimulates AP-1 activity by inhibiting a JNK phosphatase [J].
Cavigelli, M ;
Li, WW ;
Lin, AN ;
Su, B ;
Yoshioka, K ;
Karin, M .
EMBO JOURNAL, 1996, 15 (22) :6269-6279
[9]   PROOXIDANT STATES AND TUMOR PROMOTION [J].
CERUTTI, PA .
SCIENCE, 1985, 227 (4685) :375-381
[10]  
CHEN SC, 1995, CELL GROWTH DIFFER, V6, P681