Copyright
©The Author(s) 2017.
World J Gastroenterol. Jul 7, 2017; 23(25): 4569-4578
Published online Jul 7, 2017. doi: 10.3748/wjg.v23.i25.4569
Published online Jul 7, 2017. doi: 10.3748/wjg.v23.i25.4569
Figure 5 SMARCE1 is a target of miR-29a (n = 3).
A: Wild-type (WT) and mutant (MUT) 3’-UTR binding sites are shown. The mutated bases are labelled with a horizontal line; B: Relative luciferase activity was measured in HEK293 cells co-transfected WT or MUT SMARCE1 3’-UTR with miR-17 mimic or miR-control; C-E: The relative mRNA (C) and protein (D and E) levels of SMARCE1 were measured in HepG2.2.15 cells transfected with miR-29a mimics or anti-miR-29a. Data represent the mean ± SD. aP < 0.05 vs miR-control.
- Citation: Wu HJ, Zhuo Y, Zhou YC, Wang XW, Wang YP, Si CY, Wang XH. miR-29a promotes hepatitis B virus replication and expression by targeting SMARCE1 in hepatoma carcinoma. World J Gastroenterol 2017; 23(25): 4569-4578
- URL: https://www.wjgnet.com/1007-9327/full/v23/i25/4569.htm
- DOI: https://dx.doi.org/10.3748/wjg.v23.i25.4569