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by: D. Yin, Y. Gu, Y. Li, X. Wang, Q. Zhao
Amazon.com's Price: $10.95 Prices subject to change.
Binding: Digital
Format: HTML
Label: Elsevier
Manufacturer: Elsevier
Publication Date: October 10, 2006
Publisher: Elsevier
Studio: Elsevier
Editorial Review:
Product Description: This digital document is a journal article from Mut.Res.-Genetic Toxicology and Environmental Mutagenesis, published by Elsevier in 2006. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.
Description: Pentachlorophenol (PCP), a probable human carcinogen, has been heavily used as an aseptic and a biocide throughout the world, and is widely present in the environment. Recent survey in Germany revealed that the average PCP amount in the urine of general German populations was 1.04@mg/L while the peak concentration could reach up to 19.1@mg/L. PCP was reported to cause DNA damage, but whether it can be involved in inducing point mutations in genome is unknown. To determine the genotoxicity of PCP on vertebrate, we first performed acute toxicity test on zebrafish for the effect of PCP exposure. The LC'5'0 values of zebrafish exposed to PCP at 24, 48, 72 and 96h were determined to be 0.196, 0.130, 0.130 and 0.130mg/L, respectively. We then treated zebrafish with PCP for 10 days at 0 (control), 0.5, 5 and 50@mg/L, respectively, to determine whether PCP could be involved in inducing point mutations. Employing denaturing high-performance liquid chromatography analysis and DNA sequencing, we demonstrated that exposure of PCP to zebrafish at a concentration as low as 5@mg/L for 10 days elevates point mutation rate in p53 gene in liver cells. This is the first direct evidence revealing that PCP can elevate point mutation rate in the vertebrate genomes. The result implies PCP might be involved in carcinogenesis by elevating point mutation rate in the somatic genomes.
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