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基于微阵列的小鼠肝再生过程中基因表达谱的探索性分析。

Explorative analysis of the gene expression profile during liver regeneration of mouse: a microarray-based study.

机构信息

a Laboratory of Tropical Biomedicine and Biotechnology, School of Tropical Medicine and Laboratory Medicine , Hainan Medical University , Haikou , Hainan , China.

b State Key Laboratory Cultivation Base for Cell Differentiation Regulation and Henan Engineering Laboratory for Bioengineering and Drug Development , Henan Normal University , Xinxiang , Henan , China.

出版信息

Artif Cells Nanomed Biotechnol. 2019 Dec;47(1):1113-1121. doi: 10.1080/21691401.2019.1593851.

Abstract

The liver is an amazing organ due to its powerful regenerative capacity. Although many studies on liver regeneration have been documented, the detailed mechanisms remain unclear. Two-third partial hepatectomy (PH) in rodents plays a crucial role in the study of liver regeneration. In this study, the time series data of gene expression during liver regeneration in mouse were analyzed using the gene set numbered GSE6998 in GEO. A variety of bioinformatics methods, including masigPro, Weighted Gene Co-expression Network Analysis (WGCNA), spatial analysis of functional enrichment (SAFE) and ingenuity canonical pathway analysis (IPA) were used to identify and compare the significantly changed pathways, potential upstream regulators and key genes during liver regeneration. Our study showed that liver regeneration in the mouse is a coordinated process, which cell-cycle-related progress are at the centre of the interaction network involved in liver regeneration. Several candidate upstream regulators including PPARA, NFE2L2, MAD1 and CNR1 and some key genes such as Cdk1, Plk1, Cdc20, Aurka, Racgap1, Cenpa, Rrm1, Rrm2 were identified. In conclusion, these findings could contribute to revealing the molecular mechanism of liver regeneration after PH, which could provide new ideas and treatment methods for regenerative medicine, oncological drug development and oncological treatment.

摘要

肝脏因其强大的再生能力而成为一种神奇的器官。尽管已有许多关于肝脏再生的研究被记录下来,但详细的机制仍不清楚。啮齿动物的三分之二部分肝切除术(PH)在肝脏再生研究中起着至关重要的作用。在这项研究中,使用 GEO 中的基因集编号 GSE6998 分析了小鼠肝脏再生过程中基因表达的时间序列数据。使用多种生物信息学方法,包括 masigPro、加权基因共表达网络分析(WGCNA)、功能富集的空间分析(SAFE)和Ingenuity 通路分析(IPA),来识别和比较在肝脏再生过程中显著改变的途径、潜在的上游调控因子和关键基因。我们的研究表明,小鼠肝脏再生是一个协调的过程,细胞周期相关的进展是参与肝脏再生的相互作用网络的中心。鉴定出了一些候选的上游调控因子,包括 PPARA、NFE2L2、MAD1 和 CNR1,以及一些关键基因,如 Cdk1、Plk1、Cdc20、Aurka、Racgap1、Cenpa、Rrm1、Rrm2。总之,这些发现有助于揭示 PH 后肝脏再生的分子机制,为再生医学、肿瘤药物开发和肿瘤治疗提供新的思路和治疗方法。

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