Literature DB >> 16260176

Detection of initiating as well as promoting activity of chemicals by a novel cell transformation assay using v-Ha-ras-transfected BALB/c 3T3 cells (Bhas 42 cells).

Shin Asada1, Kiyoshi Sasaki, Noriho Tanaka, Ken Takeda, Makoto Hayashi, Makoto Umeda.   

Abstract

Cell transformation assay using BALB/c 3T3 cells, C3H10T1/2 cells and others, can simulate the two-stage carcinogenesis utilized for formation of transformed foci. A sensitive cell transformation assay for tumor initiators as well as promoters has been developed using a v-Ha-ras-transfected BALB/c 3T3 cell line, Bhas 42; these cells are regarded as initiated in the two-stage paradigm of carcinogenesis. To distinguish between initiation and promotion, the initiation assay involves a 2-day treatment of low-density cells, obtained one day after plating, with a test chemical, and the promotion assay involves treatment of near-confluent cells with a test chemical for a period of 12 days (Day 3-14). When Bhas 42 cells were treated with tumor initiators, N-methyl-N'-nitro-N-nitrosoguanidine and 3-methylcholanthrene, transformed foci were induced in the initiation assay but not in the promotion assay. In contrast, tumor promoters, 12-O-tetradecanoylphorbol-13-acetate, lithocholic acid and okadaic acid, gave negative responses in the initiation assay but positive responses in the promotion assay. The results were reproducible with various treatment protocols. Sixteen polycyclic aromatic hydrocarbons were examined using both assays. Benzo[a]pyrene and 7,12-dimethylbenz[a]anthracene induced focus formation only in the initiation assay. Increase of focus formation was observed in the promotion assay with benzo[e]pyrene, benzo[ghi]perylene, 1-nitropyrene and pyrene. Benz[a]anthracene, benz[b]anthracene, chrysene and perylene showed positive responses in both initiation and promotion assays. Results of initiation and promotion assays of acenaphthylene, anthracene, coronene, 9,10-diphenylanthracene, naphthalene and phenanthrene were negative or equivocal. The present Bhas assays for the detection of either/both initiating and promoting activities of chemicals are sensitive and of high performance compared with other cell transformation assays.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 16260176     DOI: 10.1016/j.mrgentox.2005.07.011

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  6 in total

1.  Cell transformation assays for prediction of carcinogenic potential: state of the science and future research needs.

Authors:  Stuart Creton; Marilyn J Aardema; Paul L Carmichael; James S Harvey; Francis L Martin; Robert F Newbold; Michael R O'Donovan; Kamala Pant; Albrecht Poth; Ayako Sakai; Kiyoshi Sasaki; Andrew D Scott; Leonard M Schechtman; Rhine R Shen; Noriho Tanaka; Hemad Yasaei
Journal:  Mutagenesis       Date:  2011-08-17       Impact factor: 3.000

2.  Deep neural network for the determination of transformed foci in Bhas 42 cell transformation assay.

Authors:  Minami Masumoto; Ittetsu Fukuda; Suguru Furihata; Takahiro Arai; Tatsuto Kageyama; Kiyomi Ohmori; Shinichi Shirakawa; Junji Fukuda
Journal:  Sci Rep       Date:  2021-12-02       Impact factor: 4.379

3.  Altered gene expression and miRNA expression associated with cancerous IEC-6 cell transformed by MNNG.

Authors:  Bo Zhang; Xukai Wang; Yan Wang
Journal:  J Exp Clin Cancer Res       Date:  2009-04-28

4.  Improvement of the BALB/c-3T3 cell transformation assay: a tool for investigating cancer mechanisms and therapies.

Authors:  Doerte Poburski; René Thierbach
Journal:  Sci Rep       Date:  2016-09-09       Impact factor: 4.379

5.  Application of Text Mining in Risk Assessment of Chemical Mixtures: A Case Study of Polycyclic Aromatic Hydrocarbons (PAHs).

Authors:  Imran Ali; Kristian Dreij; Simon Baker; Johan Högberg; Anna Korhonen; Ulla Stenius
Journal:  Environ Health Perspect       Date:  2021-06-24       Impact factor: 9.031

6.  Gene Expression over Time during Cell Transformation Due to Non-Genotoxic Carcinogen Treatment of Bhas 42 Cells.

Authors:  Kiyomi Ohmori; Asuka Kamei; Yuki Watanabe; Keiko Abe
Journal:  Int J Mol Sci       Date:  2022-03-16       Impact factor: 5.923

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.