MicroRNAs and their predicted target messenger RNAs are deregulated by Exposure to a Carcinogenic Dose of Comfrey in Rat Liver
✍ Scribed by Zhiguang Li; James C. Fuscoe; Tao Chen
- Book ID
- 102833248
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 765 KB
- Volume
- 52
- Category
- Article
- ISSN
- 0893-6692
- DOI
- 10.1002/em.20645
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✦ Synopsis
Abstract
MicroRNAs (MiRNAs) are small noncoding RNAs that function as regulators of gene expression to control cell growth and differentiation. In this study, we analyzed miRNA and mRNA expression in the livers of rats treated with a carcinogenic dose of comfrey (Symphytum officinale) for 12 weeks. Groups of six rats were fed a normal diet or a diet containing 8% comfrey root. The animals were sacrificed 1 day after the last treatment and the livers were isolated for miRNA expression analysis using LC Sciences miRNA microarrays and for mRNA expression analysis using Affymetrix rat genome microarrays. MiRNA expression levels were significantly changed by comfrey treatment. The treated samples were separated clearly from the control samples in both principal component analysis (PCA) and hierarchical clustering analysis (HCA). Quantitative measurements of seven miRNAs using TaqMan real‐time PCR were consistent with the microarray results in terms of fold‐change and the direction of the change in expression. Forty‐five miRNAs (P < 0.01) and 1,921 mRNAs (q = 0) were significantly changed by comfrey treatment. Using a target prediction algorithm, 434 differentially expressed genes (DEGs) were predicted to be targeted by the differentially expressed miRNAs (DEMs). The DEM‐targeted DEGs were more likely to be involved in carcinogenesis than the DEGs that were not targeted by the DEMs. The nontargeted DEGs were enriched in noncancer‐related biological processes. Our data suggest that comfrey may exert its carcinogenic effects by disturbing miRNA expression resulting in altered mRNA levels of the DEM‐targeted genes that are functionally associated with carcinogenesis. Environ. Mol. Mutagen., 2011. © Published 2011 Wiley‐Liss, Inc.