EFFECT OF CURCUMIN ON 12-O-TETRADECANOYLPHORBOL-13-ACETATE-INDUCED AND ULTRAVIOLET-B LIGHT-INDUCED EXPRESSION OF C-JUN AND C-FOS IN JB6 CELLS AND IN MOUSE EPIDERMIS

被引:107
作者
LU, YP [1 ]
CHANG, RL [1 ]
LOU, YR [1 ]
HUANG, MT [1 ]
NEWMARK, HL [1 ]
REUHL, KR [1 ]
CONNEY, AH [1 ]
机构
[1] RUTGERS STATE UNIV,COLL PHARM,DEPT PHARMACOL & TOXICOL,NEUROTOXICOL LABS,PISCATAWAY,NJ 08855
关键词
D O I
10.1093/carcin/15.10.2363
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Expression of c-jun protein (c-Jun) was observed in normally proliferating JB6 cells but not in confluent cells. Reduction of the serum concentration from 5% to 2% in the cell culture medium caused JB6 cells to enter a quiescent non-proliferating state and down-regulated the expression of c-Jun. Treatment of quiescent JB6 cells with 12-O-tetradecanoylphorbol-13-acetate (TPA) (10 ng/ml) for 24 h markedly stimulated the formation of c-Jun and caused morphological changes. Treatment of JB6 cells with TPA for 48 h resulted in transformed foci with mixed cell populations. Although some cells in these foci expressed high levels of c-Jun, many other cells did not. The increased expression of c-Jun and morphological changes observed at 24 h after treatment of JB6 cells with TPA (10 ng/ml) was inhibited by curcumin (10 nmol/ml). Treatment of JB6 cells with 2.5, 5 or 10 nmol curcunmin/ml inhibited the formation of TPA-induced anchorage-independent colonies that grow in soft agar by 31%, 43% and 77%, respectively. Although inhibition of cell proliferation was not observed with 2.5 mmol curcumin/ml, higher concentrations did inhibit cell proliferation. Topical application of 5 mnol TPA to the backs of CD-1 mice once a day for 5 days caused epidermal hyperplasia and the levels of c-Jun were increased in the suprabasal layer of the epidermis and in the muscle layer of the dermis. This treatment also increased c-fos protein (c-Fos) expression in the muscle layer, but there was little or no increase in the expression of c-Fos in the basal or suprabasal layer of the epidermis. Topical application of 10 mu mol curcumin together with 5 nmol TPA once a day for 5 days strongly inhibited TPA-induced epidermal hyperplasia and c-Jun and c-Fos expression. A single application of 180 mJ/cm(2) of ultraviolet B light (UVB) to the backs of SKH-1 mice caused epidermal hyperplasia and expression of c-Fos and c-Jun in the muscle layer of the dermis and of c-Fos in the suprabasal layer of the epidermis. Maximum effects were observed at 6 days after UVB exposure. Application of 10 mu mol curcumin to mouse skin twice a day for 5 days immediately after UVB exposure had only a small/variable inhibitory effect on UVB-induced increases in the expression of c-Fos and c-Jun and on epidermal hyperplasia. These data suggest that induction of hyperplasia and c-Jun and c-Fos expression in mouse skin by TPA and UVB may involve different pathways and that inhibition of TPA-induced skin tumorigenesis by curcumin may be associated with inhibition of TPA-induced increases in the expression of c-Jun and c-Fos.
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页码:2363 / 2370
页数:8
相关论文
共 46 条
  • [1] REDOX REGULATION OF FOS AND JUN DNA-BINDING ACTIVITY INVITRO
    ABATE, C
    PATEL, L
    RAUSCHER, FJ
    CURRAN, T
    [J]. SCIENCE, 1990, 249 (4973) : 1157 - 1161
  • [2] THE JUN PROTO-ONCOGENE IS POSITIVELY AUTOREGULATED BY ITS PRODUCT, JUN/AP-1
    ANGEL, P
    HATTORI, K
    SMEAL, T
    KARIN, M
    [J]. CELL, 1988, 55 (05) : 875 - 885
  • [3] PHORBOL ESTER INDUCIBLE GENES CONTAIN A COMMON CIS ELEMENT RECOGNIZED BY A TPA-MODULATED TRANS-ACTING FACTOR
    ANGEL, P
    IMAGAWA, M
    CHIU, R
    STEIN, B
    IMBRA, RJ
    RAHMSDORF, HJ
    JONAT, C
    HERRLICH, P
    KARIN, M
    [J]. CELL, 1987, 49 (06) : 729 - 739
  • [4] DIFFERENTIAL C-JUN EXPRESSION IN RESPONSE TO TUMOR PROMOTERS IN JB6 CELLS SENSITIVE OR RESISTANT TO NEOPLASTIC TRANSFORMATION
    BENARI, ET
    BERNSTEIN, LR
    COLBURN, NH
    [J]. MOLECULAR CARCINOGENESIS, 1992, 5 (01) : 62 - 74
  • [5] APL/JUN FUNCTION IS DIFFERENTIALLY INDUCED IN PROMOTION-SENSITIVE AND RESISTANT JB6 CELLS
    BERNSTEIN, LR
    COLBURN, NH
    [J]. SCIENCE, 1989, 244 (4904) : 566 - 569
  • [6] BLUMBERG PM, 1988, CANCER RES, V48, P1
  • [7] ACTIVATION OF PROTEIN-KINASE-C DECREASES PHOSPHORYLATION OF C-JUN AT SITES THAT NEGATIVELY REGULATE ITS DNA-BINDING ACTIVITY
    BOYLE, WJ
    SMEAL, T
    DEFIZE, LHK
    ANGEL, P
    WOODGETT, JR
    KARIN, M
    HUNTER, T
    [J]. CELL, 1991, 64 (03) : 573 - 584
  • [8] BROWN PH, 1993, ONCOGENE, V8, P877
  • [9] BUSCHER M, 1988, ONCOGENE, V3, P301
  • [10] CARTER TH, 1987, MECHANISMS ENV CARCI, V1, P47