Identification of tumor promotion marker genes for predicting tumor promoting potential of chemicals in BALB/c 3T3 cells

被引:9
作者
Maeshima, Hideki [1 ]
Ohno, Katsutoshi [1 ]
Tanaka-Azuma, Yukimasa [1 ]
Nakano, Shigeru [1 ]
Yamada, Toshihiro [1 ]
机构
[1] Nissin Food Prod Co Ltd, Food Safety Res Inst, Shiga 5250055, Japan
关键词
DNA microarray; In vitro screening assay; Molecular marker; Transformation assay; Tumor promotion; PROTEIN-KINASE; CELL-PROLIFERATION; TRANSFORMATION; EXPRESSION; RECEPTOR; SYSTEM; CARCINOGENESIS; CLASSIFICATION; INHIBITION; ANNOTATION;
D O I
10.1016/j.tiv.2008.10.005
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Tumor promoters Call Cause development of tumors in initiated cells and the majority of them are nongenotoxic carcinogens. The detection of tumor promoters is important for the prevention of cancer. The in vitro two-stage transformation assay, using BALB/c 3T3 cells, is a useful system, and benefits from a convenient protocol and high predictability of mammalian carcinogenicity. But these assays are time-consuming and often require expertise for microscopic observation. To construct an in vitro tumor promoting activity test system, we performed large-scale gene expression analyses, using DNA microarrays, of BALB/c 3T3 cells following treatment with mile chemicals that are known to induce tumor promotion: TPA, zinc chloride, sodium orthovanadate, okadaic acid, insulin, lithocolic acid, phenobarbital sodium, sodium saccharide, sodium arsenite. As a result of DNA microarray and real time PCR analyses, 22 marker genes were identified. These consisted of genes related to cell cycle, regulation of transcription, antiapoptosis, and positive regulation of cell proliferation. There was a correlation between these 22 marker genes and the cell transformation assay results in BALB/c 3T3 cells. These results suggest that this tumor promoting activity test system, based oil 22 marker genes, can become a valuable tool for screening potential tumor promoters. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:148 / 157
页数:10
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