Document Detail


Radical mechanisms in nitrosamine- and nitrosamide-induced whole-genome gene expression modulations in Caco-2 cells.
MedLine Citation:
PMID:  20403970     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
N-nitroso compounds (NOCs) may be implicated in human colon carcinogenesis, but the toxicological mechanisms involved have not been elucidated. Because it was previously demonstrated that nitrosamines and nitrosamides, representing two classes of NOC, induce distinct gene expression effects in colon cells that are particularly related to oxidative stress, we hypothesized that different radical mechanisms are involved. Using electron spin resonance spectroscopy, we investigated the radical-generating properties of genotoxic NOC concentrations in human colon adenocarcinoma cells (Caco-2). Cells were exposed to nitrosamides (N-methyl-N'-nitro-N-nitrosoguanidine and N-methyl-N-nitrosourea) or nitrosamines (N-nitrosodiethylamine, N-nitrosodimethylamine, N-nitrosopiperidine, and N-nitrosopyrrolidine). Nitrosamines caused formation of reactive oxygen species (ROS) and carbon-centered radicals, which was further stimulated in the presence of Caco-2 cells. N-methyl-N-nitrosourea exposure resulted in a small ROS signal, and formation of nitrogen-centered radicals (NCRs), also stimulated by Caco-2 cells. N-methyl-N'-nitro-N-nitrosoguanidine did not cause radical formation at genotoxic concentrations, but at increased exposure levels, both ROS and NCR formation was observed. By associating gene expression patterns with ROS formation, several cellular processes responding to nitrosamine exposure were identified, including apoptosis, cell cycle blockage, DNA repair, and oxidative stress. These findings suggest that following NOC exposure in Caco-2 cells, ROS formation plays an important role in deregulation of gene expression patterns that may be relevant for the process of chemical carcinogenesis in the human colon, in addition to the role of DNA alkylation.
Authors:
Dennie G A J Hebels; Jacob J Briedé; Roongnapa Khampang; Jos C S Kleinjans; Theo M C M de Kok
Publication Detail:
Type:  Journal Article     Date:  2010-04-19
Journal Detail:
Title:  Toxicological sciences : an official journal of the Society of Toxicology     Volume:  116     ISSN:  1096-0929     ISO Abbreviation:  Toxicol. Sci.     Publication Date:  2010 Jul 
Date Detail:
Created Date:  2010-06-18     Completed Date:  2010-10-21     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9805461     Medline TA:  Toxicol Sci     Country:  United States    
Other Details:
Languages:  eng     Pagination:  194-205     Citation Subset:  IM    
Affiliation:
Department of Health Risk Analysis and Toxicology, Maastricht University, Maastricht, The Netherlands. d.hebels@grat.unimaas.nl
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Caco-2 Cells
Electron Spin Resonance Spectroscopy
Genome-Wide Association Study*
Humans
Nitrosamines / toxicity*
Nitroso Compounds / toxicity*
Oligonucleotide Array Sequence Analysis
Reactive Oxygen Species / metabolism
Chemical
Reg. No./Substance:
0/Nitrosamines; 0/Nitroso Compounds; 0/Reactive Oxygen Species; 0/nitrosamides

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Human constitutive androstane receptor (CAR) and pregnane X receptor (PXR) support the hypertrophic ...
Next Document:  Proteomic and functional analysis of the noncanonical poly(A) polymerase Cid14.