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[肝纤维化发生分子机制中Cxcl12、Tweak、Notch1和Yap mRNA表达水平之间的关系]

[Relationships between Cxcl12, Tweak, Notch1, and Yap mRNA Expression Levels in Molecular Mechanisms of Liver Fibrogenesis].

作者信息

Lebedeva E I, Shchastniy A T, Babenka A S, Zinovkin D A

机构信息

Vitebsk State Order of Peoples' Friendship Medical University, Vitebsk, 210009 Belarus.

Belarussian State Medical University, Minsk, 220116 Belarus.

出版信息

Mol Biol (Mosk). 2024 Jan-Feb;58(1):130-140.

PMID:38943584
Abstract

Current data on the molecular mechanisms of liver fibrosis and cirrhosis fail to fully explain all stages of their development. Interactions between individual genes and signaling pathways are known to play an important role in their functions. However, data on their relationships are insufficient and often contradictory. For the first time, mRNA expression of Notch1, Notch2, Yap1, Tweak (Tnfsf12), Fn14 (Tnfrsf12a), Ang, Vegfa, Cxcl12 (Sdf), Nos2, and Mmp-9 was studied in detail at several stages of thioacetamide-induced liver fibrosis in Wistar rats. A factor analysis isolated three factors, which combined highly correlated target genes. The first factor included four genes: Cxcl12 (r = 0.829, p < 0.05), Tweak (r = 0.841, p < 0.05), Notch1 (r = 0.848, p < 0.05), and Yap1 (r = 0.921, p < 0.05). The second factor described the correlation between Mmp-9 (r = 0.791, p < 0.05) and Notch2 (r = 0.836, p < 0.05). The third factor included Ang (r = 0.748, p < 0.05) and Vegfa (r = 0.679, p < 0.05). The Nos2 and Fn14 genes were not included in any of the factors. The gene grouping by mRNA expression levels made it possible to assume a pathogenetic relationship between their products in the development of fibrotic changes due to liver toxicity.

摘要

目前关于肝纤维化和肝硬化分子机制的数据未能充分解释其发展的所有阶段。已知单个基因与信号通路之间的相互作用在其功能中起重要作用。然而,关于它们之间关系的数据不足且常常相互矛盾。首次在Wistar大鼠硫代乙酰胺诱导的肝纤维化的几个阶段详细研究了Notch1、Notch2、Yap1、Tweak(Tnfsf12)、Fn14(Tnfrsf12a)、Ang、Vegfa、Cxcl12(Sdf)、Nos2和Mmp-9的mRNA表达。因子分析分离出三个因子,这些因子组合了高度相关的靶基因。第一个因子包括四个基因:Cxcl12(r = 0.829,p < 0.05)、Tweak(r = 0.841,p < 0.05)、Notch1(r = 0.848,p < 0.05)和Yap1(r = 0.921,p < 0.05)。第二个因子描述了Mmp-9(r = 0.791,p < 0.05)和Notch2(r = 0.836,p < 0.05)之间的相关性。第三个因子包括Ang(r = 0.748,p < 0.05)和Vegfa(r = 0.679,p < 0.05)。Nos2和Fn14基因未包含在任何一个因子中。根据mRNA表达水平对基因进行分组,使得可以假设它们的产物在肝毒性引起的纤维化变化发展过程中存在致病关系。

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