MicroRNA-21/PTEN/Akt axis in the fibrogenesis of biliary atresia

被引:44
作者
Shen, Wenjun [1 ]
Chen, Gong [1 ]
Dong, Rui [1 ]
Zhao, Rui [1 ]
Zheng, Shan [1 ]
机构
[1] Fudan Univ, Childrens Hosp, Dept Pediat Surg, Shanghai 201102, Peoples R China
关键词
Biliary atresia; MicroRNA; Liver fibrosis; HEPATIC STELLATE CELLS; NF-KAPPA-B; LIVER FIBROSIS; MESENCHYMAL TRANSITION; APOPTOSIS; MIR-21; PHOSPHORYLATION; EXPRESSION; DISEASE; TARGET;
D O I
10.1016/j.jpedsurg.2014.09.009
中图分类号
R72 [儿科学];
学科分类号
100202 [儿科学];
摘要
Background: MicroRNAs (miRNAs) are short, noncoding RNA molecules that act as post-transcriptional negative regulators of target mRNAs. Increasing evidence suggests that miRNAs are involved in liver fibrotic processes. Biliary atresia (BA) is characterized by rapid and progressive liver fibrosis. Therefore, we investigated the role of miRNA-21in the pathogenesis of BA. Methods: We collected liver samples from patients with BA or liver trauma to examine the role of miRNA-21. We examined RNA expression of miRNA-21, phosphatase and tensin homolog deleted on chromosome ten (PTEN), and a-smooth muscle actin (alpha-SMA) in liver tissue using real-time fluorescence quantitative PCR. Western blot analyses and immunohistochemical staining were performed to evaluate protein expression of PTEN, a-SMA, and phosphorylated AKT in liver. Results: We found that miRNA-21 was upregulated in liver samples from BA patients, whereas PTEN negatively correlated with suppression of the 3 '-untranslated region (3 '-UTR). Activation of the downstream AKT pathway provoked liver fibrosis by enhancing a-SMA levels. Conclusions: The miRNA-21/PTEN/AKT axis promotes the fibrosis process in BA, which might be a potential therapeutic target to improve the prognosis of patients with BA. (C) 2014 Published by Elsevier Inc.
引用
收藏
页码:1738 / 1741
页数:4
相关论文
共 28 条
[1]
Role of miR-21 in the pathogenesis of atrial fibrosis [J].
Adam, Oliver ;
Loehfelm, Bjoern ;
Thum, Thomas ;
Gupta, Shashi K. ;
Puhl, Sarah-Lena ;
Schaefers, Hans-Joachim ;
Boehm, Michael ;
Laufs, Ulrich .
BASIC RESEARCH IN CARDIOLOGY, 2012, 107 (05)
[2]
PI3-K/AKT regulation of NF-κB signaling events in suppression of TNF-induced apoptosis [J].
Burow, ME ;
Weldon, CB ;
Melnik, LI ;
Duong, BN ;
Collins-Burow, BM ;
Beckman, BS ;
McLachlan, JA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 271 (02) :342-345
[3]
14-3-3 proteins and survival kinases cooperate to inactivate BAD by BH3 domain phosphorylation [J].
Datta, SR ;
Katsov, A ;
Hu, L ;
Petros, A ;
Fesik, SW ;
Yaffe, MB ;
Greenberg, ME .
MOLECULAR CELL, 2000, 6 (01) :41-51
[4]
Akt phosphorylation of BAD couples survival signals to the cell-intrinsic death machinery [J].
Datta, SR ;
Dudek, H ;
Tao, X ;
Masters, S ;
Fu, HA ;
Gotoh, Y ;
Greenberg, ME .
CELL, 1997, 91 (02) :231-241
[5]
Evidence for the epithelial to mesenchymal transition in biliary atresia fibrosis [J].
Diaz, Rosalyn ;
Kim, Ji Won ;
Hui, Jia-Ji ;
Li, Zhaodong ;
Swain, Gary P. ;
Fong, Keith S. K. ;
Csiszar, Katalin ;
Russo, Pierre A. ;
Rand, Elizabeth B. ;
Furth, Emma E. ;
Wells, Rebecca G. .
HUMAN PATHOLOGY, 2008, 39 (01) :102-115
[6]
Haafiz AB, 2010, EXPERT REV GASTROENT, V4, P335, DOI [10.1586/egh.10.29, 10.1586/EGH.10.29]
[7]
MicroRNA Profiling Identifies miR-29 as a Regulator of Disease-associated Pathways in Experimental Biliary Atresia [J].
Hand, Nicholas J. ;
Horner, Amber M. ;
Master, Zankhana R. ;
Boateng, LaTasha A. ;
LeGuen, Claire ;
Uvaydova, Marina ;
Friedman, Joshua R. .
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 2012, 54 (02) :186-192
[8]
Easily Missed? Biliary atresia [J].
Hartley, Jane ;
Harnden, Anthony ;
Kelly, Deirdre .
BRITISH MEDICAL JOURNAL, 2010, 340
[9]
miR-21 is a Critical Therapeutic Target for Renal Fibrosis [J].
He, Yong ;
Huang, Cheng ;
Li, Jun .
CELL BIOCHEMISTRY AND BIOPHYSICS, 2014, 68 (03) :635-636
[10]
Involvement of C/EBP-α gene in in vitro activation of rat hepatic stellate cells [J].
Huang, GC ;
Zhang, JS ;
Tang, QQ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 324 (04) :1309-1318