Copyright
©The Author(s) 2022.
World J Gastroenterol. May 28, 2022; 28(20): 2184-2200
Published online May 28, 2022. doi: 10.3748/wjg.v28.i20.2184
Published online May 28, 2022. doi: 10.3748/wjg.v28.i20.2184
Figure 3 miR-3121-3p is downregulated in colorectal cancer.
A: We used three websites (miRDB, DIANA and LncRNAMAP) to predict 15 microRNAs with binding sites for TNFRSF10A-AS1; B: miR-3121-3p expression was increased in cells transfected with si-lnc and decreased in cells transfected with oe-lnc; C: miR-3121-3p was downregulated in colorectal cancer tumor tissues compared to matched nontumor tissues (n = 40); D: Levels of miR-3121-3p in colon cancer cell lines were detected by quantitative real-time polymerase chain reaction; E: Schematic illustration of the predicted binding sites of miR-3121-3p in the TNFRSF10A-AS1 sequence; F: Relative luciferase activities after cotransfection with TNFRSF10A-AS1-WT, TNFRSF10A-AS1-MUT, miR-3121-3p mimics or NC in DLD1 cells. WT: Wild-type; MUT: Mutant.
- Citation: Wang DD, Sun DL, Yang SP, Song J, Wu MY, Niu WW, Song M, Zhang XL. Long noncoding RNA TNFRSF10A-AS1 promotes colorectal cancer through upregulation of HuR. World J Gastroenterol 2022; 28(20): 2184-2200
- URL: https://www.wjgnet.com/1007-9327/full/v28/i20/2184.htm
- DOI: https://dx.doi.org/10.3748/wjg.v28.i20.2184