Protection against ultraviolet B- and C-induced DNA damage and skin carcinogenesis by the flowers of Prunus persica extract

被引:22
作者
Heo, MY [1 ]
Kim, SH
Yang, HE
Lee, SH
Jo, BK
Kim, HP
机构
[1] Kangwon Natl Univ, Coll Pharm, Chunchon 200701, South Korea
[2] Coreana Cosmet Co, R&D Ctr, Cheonan 333830, South Korea
关键词
UV-induced DNA damage; flowers of Prunus persica (Rosaceae); single cell gel electrophoresis; COMET assay; skin carcinogenesis; tumor incidence; tumor multiplicity;
D O I
10.1016/S1383-5718(01)00218-2
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 0836 [生物工程]; 090102 [作物遗传育种]; 100705 [微生物与生化药学];
摘要
The ethanol extract of the flowers of Prunus persica (Ku-35) (50-200 mug/ml) was found to inhibit UVB- as well as UVC-induced DNA damage measured by the COMET assay in the skin fibroblast cell (NIH/3T3). In addition, Ku-35 inhibited UVB- or UVC-induced lipid peroxidation, especially against UVB-induced peroxidation at higher than 10 mug/ml. We also evaluated the protective effect of Ku-35 against UVB-induced non-melanoma skin cancer in mice. Ku-35 was applied topically before UVB exposure, and its effects on tumor incidence (% of mice with tumors) and tumor multiplicity (number of tumors per mouse) were evaluated. The application of Ku-35 clearly resulted in a delay of tumor development compared to the control. In tumor incidence, 100% mice in the control group and the low dose treatment of Ku-35 had tumors, whereas 94.1% of the mice had tumors after the high dose treatment of Ku-35 at the end of experiment (28 weeks). In tumor multiplicity, low and high treatments of Ku-35 resulted in 25.9 and 53.9% reduction at the end of the experiment (P < 0.05, one-way analysis of variance (ANOVA)). The present data indicate that Ku-35 protects against photogencitoxicity in NIH/3T3 fibroblasts. The possible action mechanism of Ku-35 may be through its anti-oxidant activity without pro-oxidant effect. Ku-35 can also show a delay of tumor development against UVB-induced skin carcinogenesis. These results suggest that Ku-35 extract may be useful for protecting UV-induced DNA damage and carcinogenesis when topically applied. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:47 / 59
页数:13
相关论文
共 35 条
[1]
Chemoprevention of photocarcinogenesis [J].
Agarwal, R ;
Mukhtar, H .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1996, 63 (04) :440-444
[2]
Birt DF, 1997, ANTICANCER RES, V17, P85
[3]
Buege J A, 1978, Methods Enzymol, V52, P302
[4]
ACTION SPECTRUM FOR THE FORMATION OF ENDONUCLEASE-SENSITIVE SITES AND (6-4) PHOTOPRODUCTS INDUCED IN A DNA FRAGMENT BY ULTRAVIOLET-RADIATION [J].
CHAN, GL ;
PEAK, MJ ;
PEAK, JG ;
HASELTINE, WA .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 1986, 50 (04) :641-648
[5]
The chemistry and biological effects of flavonoids and phenolic acids [J].
Croft, KD .
TOWARDS PROLONGATION OF THE HEALTHY LIFE SPAN: PRACTICAL APPROACHES TO INTERVENTION, 1998, 854 :435-442
[6]
Decker EA, 1997, NUTR REV, V55, P396, DOI 10.1111/j.1753-4887.1997.tb01580.x
[7]
Sunscreens and photocarcinogenesis: An objective assessment [J].
Elmets, CA ;
Anderson, CY .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1996, 63 (04) :435-440
[8]
FREEMAN RG, 1978, NATL CANCER I MONOGR, V50, P27
[9]
Girotti A W, 1985, J Free Radic Biol Med, V1, P87
[10]
EVIDENCE THAT PYRIMIDINE DIMERS IN DNA CAN GIVE RISE TO TUMORS [J].
HART, RW ;
SETLOW, RB ;
WOODHEAD, AD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (12) :5574-5578