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©The Author(s) 2025.
World J Gastroenterol. Apr 28, 2025; 31(16): 104305
Published online Apr 28, 2025. doi: 10.3748/wjg.v31.i16.104305
Published online Apr 28, 2025. doi: 10.3748/wjg.v31.i16.104305
Figure 4 SLC7A11 is a direct target of lncRNA FTX/miR-625-5p signaling axis.
A: The potential binding site between SLC7A11 and miR-625-5p predicted by Starbase; B: Pearson's correlation analysis was performed to determine the correlation between SLC7A11 and lncRNA FTX expression; C: SLC7A11 expression in colon cancer, rectal cancer, and paracancerous tissues; D: Relative expression of SLC7A11 in HT29R and HCT116R cells; E: Relative expression of SLC7A11 in HT29R-shFTX and HCT116R-shFTX cell lines; F: The targeting relationship between miR-625-5p and SLC7A11 was confirmed by dual-luciferase reporter assay in HT29R and HCT116R cells; G: Expression levels of SLC7A11 in HT29R-shFTX and HCT116R-shFTX cells with or without transfection of miR625-5p were determined by Western blotting. aP < 0.05 and bP < 0.01. NC: Negative control.
- Citation: Dai Q, Qu TY, Yang JL, Leng J, Fang L, Zhu QQ, Wu KB, Wu J, Ma JJ, Yu HF. LncRNA FTX promotes colorectal cancer radioresistance through disturbing redox balance and inhibiting ferroptosis via miR-625-5p/SCL7A11 axis. World J Gastroenterol 2025; 31(16): 104305
- URL: https://www.wjgnet.com/1007-9327/full/v31/i16/104305.htm
- DOI: https://dx.doi.org/10.3748/wjg.v31.i16.104305