Meier Michelle, Knudsen Anders Riegels, Andersen Kasper Jarlhelt, Bjerregaard Niels Christian, Jensen Uffe Birk, Mortensen Frank Viborg
Department of Surgical Gastroenterology, Section for Upper Gastrointestinal and Hepato-Pancretico-Biliary Surgery, Aarhus University Hospital, Aarhus, Denmark.
Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.
Gene Expr. 2017 Nov 27;17(4):289-299. doi: 10.3727/105221617X695825. Epub 2017 May 9.
Extended hepatectomies may result in posthepatectomy liver failure, a condition with a high mortality. The main purpose of the present study was to investigate and compare the gene expression profiles in rats subjected to increasing size of partial hepatectomy (PH). Thirty Wistar rats were subjected to 30%, 70%, or 90% PH, sham operation, or no operation. Twenty-four hours following resection, liver tissue was harvested and genome-wide expression analysis was performed. Cluster analysis revealed two main groupings, one containing the PH(90%) and one containing the remaining groups [baseline, sham, PH(30%), and PH(70%)]. Categorization of specific affected molecular pathways in the PH(90%) group revealed a downregulation of cellular homeostatic function degradation and biosynthesis, whereas proliferation, cell growth, and cellular stress and injury were upregulated in the PH(90%) group. After PH(90%), the main upregulated pathways were mTOR and ILK. The main activated upstream regulators were hepatocyte growth factor and transforming growth factor. With decreasing size of the future liver remnant, the liver tended to prioritize expression of genes involved in cell proliferation and differentiation at the expense of genes involved in metabolism and body homeostasis. This prioritizing may be an essential molecular explanation for posthepatectomy liver failure.
扩大肝切除术可能导致肝切除术后肝衰竭,这是一种死亡率很高的病症。本研究的主要目的是调查和比较接受不同程度肝部分切除术(PH)的大鼠的基因表达谱。30只Wistar大鼠分别接受30%、70%或90%的PH手术、假手术或不做手术。切除术后24小时,采集肝脏组织并进行全基因组表达分析。聚类分析显示出两个主要分组,一组包含PH(90%)组,另一组包含其余组[基线组、假手术组、PH(30%)组和PH(70%)组]。对PH(90%)组中特定受影响分子途径的分类显示,细胞稳态功能降解和生物合成下调,而PH(90%)组中增殖、细胞生长以及细胞应激和损伤上调。PH(90%)术后,主要上调的途径是mTOR和ILK。主要激活的上游调节因子是肝细胞生长因子和转化生长因子。随着未来肝剩余体积的减小,肝脏倾向于优先表达参与细胞增殖和分化的基因,而牺牲参与代谢和身体稳态的基因。这种优先排序可能是肝切除术后肝衰竭的一个重要分子解释。