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©The Author(s) 2022.
World J Stem Cells. Jul 26, 2022; 14(7): 539-555
Published online Jul 26, 2022. doi: 10.4252/wjsc.v14.i7.539
Published online Jul 26, 2022. doi: 10.4252/wjsc.v14.i7.539
Figure 3 miR-3682-3p promotes the tumorigenicity of hepatocellular carcinoma cells in vivo.
A: The tumorigenic rate of different concentrations of hepatocellular carcinoma cells (n = 5); B: Tumors in the miR-3682-3p overexpression group weighed significantly more than those of the control group (n = 5); C: Detection of miR-3682-3p expression in tumor tissues by RT-qPCR; D: Survival analysis revealed that miR-3682-3p antagomir prolongs the survival time of mice (n = 10, log-rank test); E: Immunohistochemical staining for stem cell-associated markers (SOX2 and OCT4) in xenograft tumors (n = 5) (× 100 magnification scale bar: 200 µm; × 400 magnification scale bar: 50 µm). bP < 0.01. NC: Negative control; HE: Hematoxylin and eosin.
- Citation: Chen Q, Yang SB, Zhang YW, Han SY, Jia L, Li B, Zhang Y, Zuo S. miR-3682-3p directly targets FOXO3 and stimulates tumor stemness in hepatocellular carcinoma via a positive feedback loop involving FOXO3/PI3K/AKT/c-Myc. World J Stem Cells 2022; 14(7): 539-555
- URL: https://www.wjgnet.com/1948-0210/full/v14/i7/539.htm
- DOI: https://dx.doi.org/10.4252/wjsc.v14.i7.539