Comparative effects of eight varieties of blackberry on mutagenesis

被引:18
作者
Tate, P
Kuzmar, A
Smith, SW
Wedge, DE
Larcom, LL [1 ]
机构
[1] Clemson Univ, Dept Biol Sci, Clemson, SC 29634 USA
[2] Clemson Univ, Dept Phys & Astron, Clemson, SC 29634 USA
[3] Greenville Mem Hosp Syst, Greenville, SC 29605 USA
[4] Univ Mississippi, USDA ARS, Nat Prod Utilizat Res Unit, University, MS 38677 USA
[5] Univ Mississippi, Thad Cochran Natl Ctr Nat Prod Res, University, MS 38677 USA
关键词
mutagenesis inhibition; berries; Ames assay; blackberry varieties;
D O I
10.1016/S0271-5317(03)00083-6
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Diets containing large amounts of fruits and vegetables are known to decrease the probability of developing cancer. The chemical composition of fruits can vary with their genetic characteristics and the environmental conditions under which they are cultivated. Because of this variability, different varieties of the same fruit could be expected to have different effects on processes leading to carcinogenesis. Blackberries have been shown to have anti-carcinogenic potential. Since somatic mutations play a major role in the initiation and progression of cancer, we have compared eight varieties of blackberry grown under the same conditions for their abilities to inhibit carcinogen-induced mutagenesis. Using the Ames assay, we have measured the effects of each of the eight varieties on: 1) mutation induction by 2-amino anthracene (2AA), 2) mutation induction by methyl methanesulfonate (MMS) and 3) cell survival. All varieties were found to strongly suppress 2AA mutagenesis, but have minimal effect on MMS mutagenesis. Experiments were performed with berry juice and with homogenized berries. In addition, berries extracts were acidified to-simulate changes which might be caused by the digestive process. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:971 / 979
页数:9
相关论文
共 19 条
[1]   The effects of dietary ellagic acid on rat hepatic and esophageal mucosal cytochromes P450 and phase II enzymes [J].
Ahn, D ;
Putt, D ;
Kresty, L ;
Stoner, GD ;
Fromm, D ;
Hollenberg, PF .
CARCINOGENESIS, 1996, 17 (04) :821-828
[2]   METHODS FOR DETECTING CARCINOGENS AND MUTAGENS WITH SALMONELLA-MAMMALIAN-MICROSOME MUTAGENICITY TEST [J].
AMES, BN ;
MCCANN, J ;
YAMASAKI, E .
MUTATION RESEARCH, 1975, 31 (06) :347-363
[3]   DOES CARCINOGENIC POTENCY CORRELATE WITH MUTAGENIC POTENCY IN AMES ASSAY [J].
ASHBY, J ;
STYLES, JA .
NATURE, 1978, 271 (5644) :452-455
[4]   MARKED ANTIMUTAGENIC POTENTIAL OF AQUEOUS GREEN TEA EXTRACTS - MECHANISM OF ACTION [J].
BUABBAS, A ;
CLIFFORD, MN ;
WALKER, R ;
IOANNIDES, C .
MUTAGENESIS, 1994, 9 (04) :325-331
[5]  
CUTLER SJ, 2000, BIOL ACTIVE NATURAL, P277
[6]   Metabolic activation of aromatic amine mutagens by simultaneous expression of human cytochrome P450 1A2, NADPH-cytochrome P450 reductase, and N-acetyltransferase in Escherichia coli [J].
Josephy, PD ;
Evans, DH ;
Parikh, A ;
Guengerich, FP .
CHEMICAL RESEARCH IN TOXICOLOGY, 1998, 11 (01) :70-74
[7]   ISOLATION AND IDENTIFICATION OF PRODUCTS FROM ALKYLATION OF NUCLEIC-ACIDS - ETHYL-PURINES AND ISOPROPYL-PURINES [J].
LAWLEY, PD ;
ORR, DJ ;
JARMAN, M .
BIOCHEMICAL JOURNAL, 1975, 145 (01) :73-84
[8]   INHIBITION OF N-NITROSOBENZYLMETHYLAMINE-INDUCED ESOPHAGEAL TUMORIGENESIS IN RATS BY ELLAGIC ACID [J].
MANDAL, S ;
STONER, GD .
CARCINOGENESIS, 1990, 11 (01) :55-61
[9]   INHIBITION OF AFLATOXIN-B1 MUTAGENESIS IN SALMONELLA-TYPHIMURIUM AND DNA DAMAGE IN CULTURED RAT AND HUMAN TRACHEOBRONCHIAL TISSUES BY ELLAGIC ACID [J].
MANDAL, S ;
AHUJA, A ;
SHIVAPURKAR, NM ;
CHENG, SJ ;
GROOPMAN, JD ;
STONER, GD .
CARCINOGENESIS, 1987, 8 (11) :1651-1656
[10]   Evidence for the presence of a microsomal NADH-dependent enzyme system that can bioactivate aromatic amines in the liver of rats and mice [J].
Marczylo, T ;
Ioannides, C .
TOXICOLOGY, 1999, 134 (2-3) :127-141