Activities of mycotoxins derived from Fusarium and related substances in a short-term transformation assay using v-Ha-ras-transfected BALB/3T3 cells (Bhas 42 cells)

被引:15
作者
Sakai, Ayako
Suzuki, Chihiro
Masui, Yasuko
Kurarnashi, Ai
Takatori, Kosuke
Tanaka, Noriho
机构
[1] Food & Drug Safety Ctr, Lab Cell Carcinogenic, Hatano Res Inst, Kanagawa 2578523, Japan
[2] Natl Inst Hlth Sci, Div Microbiol, Setagaya Ku, Tokyo 1588501, Japan
关键词
transformation; bhas; 42; cells; mycotoxins; fumonisin B-1; T-2; toxin; tumor promotion; TUMOR PROMOTERS; FUMONISIN B-1; MORPHOLOGICAL TRANSFORMATION; OKADAIC ACID; MUTAGENICITY; AFLATOXIN; TOXICITY; CULTURES; DEOXYNIVALENOL; SUSCEPTIBILITY;
D O I
10.1016/j.mrgentox.2007.03.005
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 ; 0836 ; 090102 ; 100705 ;
摘要
Cell transformation assays using BALB/3T3 cells can mimic the two-stage process of chemical carcinogenesis in experimental animals. A short-term transformation assay using v-Ha-ras-transfected BALB/3T3 cells (Bhas 42 cells), which was developed by Ohmori et al. and modified by Asada et al., has been reported to detect both tumor initiators and promoters as transformation initiators and promoters, respectively, with their differences based on their protocols. In this new short-term assay, we examined mycotoxins derived from Fusarium and related substances for the initiation and promotion activities of the transformation. The tested substances included deoxynivalenol, nivalenol, fusarenon-X, T-2 toxin, fumonisin B-1, fumonisin B-2, zearalenone, alpha-zearalanol, beta-zearalanol, alpha-zearalenol and beta-zearalenol. Fumonisin B-1 and T-2 toxin were positive for promoting activity in the assay. Especially, T-2 toxin was active at concentrations as low as 0.001-0.002 mu g/mL in the culture medium. From a comparison between the results of this study and published carcinogenicity assay data, it was expected that the Bhas 42 cell transformation assay had a good correlation with the two-stage carcinogenicity tests using experimental animals for estimation of the tumor-promoting activity. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:103 / 111
页数:9
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