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©The Author(s) 2015.
World J Gastroenterol. Mar 14, 2015; 21(10): 2949-2958
Published online Mar 14, 2015. doi: 10.3748/wjg.v21.i10.2949
Published online Mar 14, 2015. doi: 10.3748/wjg.v21.i10.2949
Figure 2 miR-133a inhibits proliferation, migration, and invasion and induces apoptosis in SGC-7901 and MGC-803 cells.
A: Total levels of miR-133a in SGC-7901 and MGC-803 cells transfected with synthetic miR-133a mimics or negative control mimics (bP < 0.01 vs negative control); B: Cell proliferation was analyzed using MTT assays in the SGC-7901 and MGC-803 cell lines. The assays were read every 24 h for five consecutive days following 24 h transfection (aP < 0.01 vs negative control); C: Cells that stained positive for FITC-Annexin V and negative for PI at 48 h post-transfection were scored as exhibiting early apoptosis; D: Statistical analysis of apoptotic cells (bP < 0.01 vs miR-133a); E and F: miR-133a mimics inhibit the migration and invasion of SGC-7901 and MGC-803 cells compared with negative control (aP < 0.01 vs negative control). All results represent the means ± SEM of three independent experiments.
- Citation: Gong Y, Ren J, Liu K, Tang LM. Tumor suppressor role of miR-133a in gastric cancer by repressing IGF1R. World J Gastroenterol 2015; 21(10): 2949-2958
- URL: https://www.wjgnet.com/1007-9327/full/v21/i10/2949.htm
- DOI: https://dx.doi.org/10.3748/wjg.v21.i10.2949