Trichloroethylene (TCE) is a multimedia environmental pollution that is carcinogenic in mouse liver. The ability of TCE to modulate DNA methylation and the expression of immediate-early protooncogenes was evaluated. Female B6C3F1 mice were administered 1000 mg/kg TCE by gavage 5 days/week and killed
The effect of dichloroacetic acid and trichloroacetic acid on DNA methylation and cell proliferation in B6C3F1 mice
β Scribed by Rongrong Ge; Siming Yang; Paula M. Kramer; Lianhui Tao; Michael A. Pereira
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 181 KB
- Volume
- 15
- Category
- Article
- ISSN
- 1095-6670
- DOI
- 10.1002/jbt.5
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
The chlorine disinfection byβproducts, dichloroacetic acid (DCA) and trichloroacetic acid (TCA), are carcinogenic in mouse liver. We have previously reported that DCA and TCA induced DNA hypomethylation in mouse liver. In the present study, we determined the temporal association for DNA hypomethylation and cell proliferation. Female B6C3F1 mice were administered daily doses of 500 mg/kg DCA or TCA by gavage and sacrificed at 24, 36, 48, 72, and 96 hours after the first dose. The proliferating cell nuclear antigenβlabeling index in the liver was increased at 72 and 96 hours by both DCA and TCA, that is, at 72 hours the index was 1.00 Β± 0.21, 0.51 Β± 0.11, and 0.095 Β± 0.016 for DCA, TCA, and the vehicle control, respectively. The mitotic index was also significantly increased at 96 hours. The promoter region for the cβmyc gene was hypomethylated only at 72 and 96 hours and not at the earlier sacrifices. Similarly, the methylation of the cβmyc gene in the kidney and urinary bladder was decreased only at 72 and 96 hours. In summary, enhancement of cell proliferation and decreased methylation of the cβmyc gene were first observed simultaneously at 72 hours after the start of exposure. Thus, the results support the hypothesis that DCA and TCA induce DNA hypomethylation by inducing DNA replication and preventing the methylation of the newly synthesized strands of DNA. Β© 2001 John Wiley & Sons, Inc. J Biochem Mol Toxicol 15:100β106, 2001
π SIMILAR VOLUMES
## Abstract Peroxisome proliferators in general are nongenotoxic mouse liver carcinogens for which DNA hypomethylation and altered gene expression are proposed mechanisms. Therefore, the peroxisome proliferators 2,4βdichlorophenoxyacetic acid (2,4βD), dibutyl phthalate (DBP), gemfibrozil, and Wyβ14
The effects of different liver tumor-promoting treatments (i.e., a choline-devoid, methionine-deficient (CMD) diet, phenobarbital (PB), or both) on Ha-ras and raf methylation status and expression were determined in mouse strains with different susceptibilities to liver tumor formation: the relative
Loss of chromosomes frequently accompanies the establishment of hepatic cell lines in mice. Previous cytogenetic and allelotype studies have revealed that loss of chromosomes 4 and 12 is particularly common. In the present study, fine-deletion mapping was performed for chromosome 12 using 44 liver e
The present study shows that the multifactorial genetic liability to spontaneous exencephaly in the SELH/Bc mouse strain (10-20% of embryos) also confers an elevated risk of exencephaly induced by valproic acid. Treatment of pregnant dams (600 mg/kg sodium valproate in distilled water, i.p.) during