scholarly journals Down-Regulation of MiR-127 Facilitates Hepatocyte Proliferation during Rat Liver Regeneration

PLoS ONE ◽  
2012 ◽  
Vol 7 (6) ◽  
pp. e39151 ◽  
Author(s):  
Chuanyong Pan ◽  
Huan Chen ◽  
Lianghua Wang ◽  
Shengsheng Yang ◽  
Hailong Fu ◽  
...  
2015 ◽  
Vol 14 (3) ◽  
pp. 7643-7654 ◽  
Author(s):  
C.F. Chang ◽  
W.M. Zhao ◽  
J.X. Mei ◽  
Y. Zhou ◽  
C.Y. Pan ◽  
...  

2011 ◽  
Vol 90 (3) ◽  
pp. 435-442 ◽  
Author(s):  
J. W. LI ◽  
G. P. WANG ◽  
J. Y. FAN ◽  
C. F. CHANG ◽  
C. S. XU

2018 ◽  
Vol 50 ◽  
pp. 80-89 ◽  
Author(s):  
Chunyan Zhang ◽  
Cuifang Chang ◽  
Hang Gao ◽  
Qiwen Wang ◽  
Fuchun Zhang ◽  
...  

2012 ◽  
Vol 34 (4) ◽  
pp. 391-399 ◽  
Author(s):  
Zhenchao Cheng ◽  
Lijuan Duan ◽  
Xiaoxia Hao ◽  
Zhanpeng Li ◽  
Gaiping Wang ◽  
...  

Author(s):  
Cunshuan Xu ◽  
Yanjie Yang ◽  
Junying Yang ◽  
Xiaoguang Chen ◽  
Gaiping Wang

AbstractTo explore the role of the integrin signaling pathway in hepatocytes during rat liver regeneration, the integrin signaling pathway-related gene expression profile in hepatocytes of regenerative liver was detected using Rat Genome 230 2.0 array. The chip data showed that 265 genes of the integrin signaling pathway were included by Rat Genome 230 2.0 array and 132 genes showed significant expression changes in hepatocytes of regenerative liver. The numbers of up-, down- and up/down-regulated genes were 110, 15 and 7 respectively. In addition, bioinformatics and systems biology methods were used to analyze the role of the integrin signaling pathway in hepatocytes. The analysis of gene synergy value indicated that paths 1, 8, 12, and 15 promoted hepatocyte proliferation at the priming phase of liver regeneration; paths 1, 3, 8, and 12–15 enhanced hepatocyte proliferation at the progressing phase; paths 11 and 14 promoted hepatocyte proliferation, while paths 12 and 13 reduced hepatocyte proliferation at the terminal phase. Additionally, the other 8 paths (2, 4, 5–7, 9–10, and 16) were not found to be related to liver regeneration. In conclusion, 132 genes and 8 cascades of the integrin signaling pathway participated in regulating hepatocyte proliferation during rat liver regeneration.


2019 ◽  
Vol 2019 ◽  
pp. 1-11
Author(s):  
Haijing Bai ◽  
Wei Jin ◽  
Jianlin Guo ◽  
Yi Ding ◽  
Cuifang Chang ◽  
...  

Liver regeneration is a tissue growth process after loss or injury of liver tissue, which is a compensatory hyperplasia rather than true regeneration, mainly depending on hepatocyte proliferation. Currently, a large number of studies on hepatocyte proliferation have been conducted. However, studies on the regulation of long noncoding RNA (lncRNA) on hepatocyte proliferation are still limited. To identify specially expressed lncRNA during rat liver regeneration, high-throughput sequencing technology was performed, and a total of 2446 lncRNAs and 4091 mRNAs were identified as significantly differentially expressed. Gene ontology (GO) enrichment analysis was performed to analyze the role of differentially expressed mRNAs, and 695 mRNAs were identified to be related to cell proliferation. Then, an lncRNA-mRNA coexpression network based on the differentially expressed lncRNAs and proliferation-related genes was constructed to analyze the potential function of lncRNAs on hepatocyte proliferation, and ten lncRNAs, NONRATT003557.2, NONRATT005357.2, NONRATT003292.2, NONRATT001466.2, NONRATT003289.2, NONRATT001047.2, NONRATT005180.2, NONRATT004419.2, NONRATT005336.2, and NONRATT005335.2, were selected as key regulatory factors, which may play crucial roles in hepatocyte proliferation during rat liver regeneration. Finally, a protein-protein interaction (PPI) network was established to illuminate the interaction between proliferation-related genes, and ten hub genes (Aurkb, Cdk1, Cdc20, Bub1b, Mad2l1, Kif11, Prc1, Ccna2, Top2a, and Ccnb1) were screened with the MCC method in the PPI network, which may be important biomarkers involved in the hepatocyte proliferation during rat liver regeneration. These results may provide clues for a more comprehensive understanding of the molecular mechanism of hepatocyte proliferation during rat liver regeneration.http://mts.hindawi.com/update/) in our Manuscript Tracking System and after you have logged in click on the ORCID link at the top of the page. This link will take you to the ORCID website where you will be able to create an account for yourself. Once you have done so, your new ORCID will be saved in our Manuscript Tracking System automatically."?>


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