Transcriptomics Evaluation of Hexavalent Chromium Toxicity in Human Dermal Fibroblasts
- *Corresponding Author:
- Dr. Pius Joseph
MS 3014, Molecular Carcinogenesis Laboratory
National Institute for Occupational Safety and Health (NIOSH)
1095 Willowdale Road, Morgantown, WV 26505
Fax: (304)285- 5708
E-mail: [email protected]
Received date: Janurary 05, 2011; Accepted date: February 24, 2011; Published date: February 26, 2011
Citation: Sellamuthu R, Umbright C, Chapman R, Leonard S, Li S, et al. (2011) Transcriptomics Evaluation of Hexavalent Chromium Toxicity in Human Dermal Fibroblasts. J Carcinogene Mutagene 2:116. doi: 10.4172/2157-2518.1000116
Copyright: © 2011 Sellamuthu R, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Significant exposure to hexavalent chromium, a metal with broad toxicity potential in humans, has been reported. In order to understand the mechanisms of dermal toxicity induced by hexavalent chromium, global gene expression profiling of human dermal fibroblasts exposed to potassium dichromate was performed. Microarray analysis of the gene expression profile in the fibroblasts treated with potassium dichromate identified significant differential expression of approximately 1,200 transcripts compared with the control cells. Functional categorization of the differentially expressed genes identified the enrichment of genes involved in several cellular processes, including apoptosis and oxidative stress, in the fibroblasts exposed to hexavalent chromium. Induction of apoptosis and oxidative stress in the dermal fibroblasts in response to their exposure to chromium was independently confirmed by additional experiments. The potassium dichromate-induced cytotoxicity, apoptosis, and oxidative stress were significantly blocked by the addition of ferrous sulfate, an agent known for its ability to reduce chromium to the insoluble and therefore impermeable trivalent form, to the cell culture medium. Taken together, our data provide insights into the potential mechanisms underlying the dermal toxicity of hexavalent chromium and provide experimental support for the proposed protective role of ferrous sulfate in hexavalent chromium-induced toxicity.