Comparative genomic analyses identify common molecular pathways modulated upon exposure to low doses of arsenic and cadmium

BMC Genomics

Research Article

Lisa Smeester¹  Rebecca C Fry¹  Margaret Ann Benton¹  Julia E Rager¹ 

[1] Department of Environmental Sciences and Engineering, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC, USA;

关键词: Cadmium;    Arsenic;    Arsenic Exposure;    Cadmium Exposure;    Sodium Arsenite;   

DOI  :  10.1186/1471-2164-12-173

 received in 2010-04-08, accepted in 2011-04-01,  发布年份 2011

来源: Springer

【 摘 要 】

BackgroundExposure to the toxic metals arsenic and cadmium is associated with detrimental health effects including cancers of various organs. While arsenic and cadmium are well known to cause adverse health effects at high doses, the molecular impact resulting from exposure to environmentally relevant doses of these metals remains largely unexplored.ResultsIn this study, we examined the effects of in vitro exposure to either arsenic or cadmium in human TK6 lymphoblastoid cells using genomics and systems level pathway mapping approaches. A total of 167 genes with differential expression were identified following exposure to either metal with surprisingly no overlap between the two. Real-time PCR was used to confirm target gene expression changes. The gene sets were overlaid onto protein-protein interaction maps to identify metal-induced transcriptional networks. Interestingly, both metal-induced networks were significantly enriched for proteins involved in common biological processes such as tumorigenesis, inflammation, and cell signaling. These findings were further supported by gene set enrichment analysis.ConclusionsThis study is the first to compare the transcriptional responses induced by low dose exposure to cadmium and arsenic in human lymphoblastoid cells. These results highlight that even at low levels of exposure both metals can dramatically influence the expression of important cellular pathways.

【 授权许可】

Unknown   
© Benton et al; licensee BioMed Central Ltd. 2011. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.