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Analysis of gene expression changes in relation to toxicity and tumorigenesis in the livers of Big Blue transgenic rats fed comfrey ( Symphytum officinale )

机译:饲喂康弗莱(Symphytum officinale)的大蓝色转基因大鼠肝脏中与毒性和肿瘤发生相关的基因表达变化分析。

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Background Comfrey is consumed by humans as a vegetable and a tea, and has been used as an herbal medicine for more than 2000 years. Comfrey, however, is hepatotoxic in livestock and humans and carcinogenic in experimental animals. Our previous study suggested that comfrey induces liver tumors by a genotoxic mechanism and that the pyrrolizidine alkaloids in the plant are responsible for mutation induction and tumor initiation in rat liver. Results In this study, we identified comfrey-induced gene expression profile in the livers of rats. Groups of 6 male transgenic Big Blue rats were fed a basal diet and a diet containing 8% comfrey roots, a dose that resulted in liver tumors in a previous carcinogenicity bioassay. The animals were treated for 12 weeks and sacrificed one day after the final treatment. We used a rat microarray containing 26,857 genes to perform genome-wide gene expression studies. Dietary comfrey resulted in marked changes in liver gene expression, as well as in significant decreases in the body weight and increases in liver mutant frequency. When a two-fold cutoff value and a P -value less than 0.01 were selected, 2,726 genes were identified as differentially expressed in comfrey-fed rats compared to control animals. Among these genes, there were 1,617 genes associated by Ingenuity Pathway Analysis with particular functions, and the differentially expressed genes in comfrey-fed rat livers were involved in metabolism, injury of endothelial cells, and liver injury and abnormalities, including liver fibrosis and cancer development. Conclusion The gene expression profile provides us a better understanding of underlying mechanisms for comfrey-induced hepatic toxicity. Integration of gene expression changes with known pathological changes can be used to formulate a mechanistic scheme for comfrey-induced liver toxicity and tumorigenesis.
机译:背景Comfrey被人类作为蔬菜和茶食用,并且已经被用作草药超过2000年。然而,Comfrey在牲畜和人类中具有肝毒性,在实验动物中具有致癌性。我们之前的研究表明,紫杉醇通过遗传毒性机制诱导肝脏肿瘤,而植物中的吡咯烷嗪生物碱负责大鼠肝脏的突变诱导和肿瘤引发。结果在这项研究中,我们确定了在大鼠肝脏中以康弗莱诱导的基因表达谱。每组6只雄性转基因大蓝鼠大鼠接受基础饮食和含有8%紫菜根的饮食,该剂量在先前的致癌性生物检测中导致肝肿瘤。将动物治疗12周并在最终治疗后一天处死。我们使用了包含26,857个基因的大鼠微阵列来进行全基因组基因表达研究。饮食上的f粉导致肝脏基因表达的显着变化,以及体重的显着下降和肝突变频率的增加。当选择一个两倍截止值和p值小于0.01时,被鉴定2726个基因如与对照动物相比紫草喂养大鼠差异表达。在这些基因中,有1617个通过“机能途径分析”关联的具有特定功能的基因,而在以f粉喂养的大鼠肝脏中差异表达的基因则参与了代谢,内皮细胞损伤以及肝损伤和异常,包括肝纤维化和癌症的发展。 。结论基因表达谱为我们提供了更好的了解紫杉醇诱导的肝毒性的潜在机制。基因表达变化与已知病理学变化的整合可用于制定因弗弗利诱导肝毒性和肿瘤发生的机制方案。

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