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©The Author(s) 2022.
World J Gastroenterol. Apr 28, 2022; 28(16): 1656-1670
Published online Apr 28, 2022. doi: 10.3748/wjg.v28.i16.1656
Published online Apr 28, 2022. doi: 10.3748/wjg.v28.i16.1656
Figure 6 Inhibition of miR-143-5p blocked the function of MEMO1 knockdown in gastric cancer cells.
A-D: MGC803 and SGC7901 cells were transfected with si-NC, si-MEMO1, si-MEMO1 + inhibitor NC, si-MEMO1 + miR-143-5p inhibitor, respectively. Transwell assay was employed for the detection of cell invasion and migration ability; E-G: MGC803 and SGC7901 cells were transfected with si-NC, si-MEMO1 + inhibitor NC, si-NC + miR-143-5p inhibitor, si-MEMO1 + miR-143-5p inhibitor, respectively. Wound healing assay was used to detect migration ability; H: The protein expression of MEMO1 was detected by western blot assay after transfecting with miR-143-5p mimics or si-cancer susceptibility 20; I: Western blot was utilized to detect the expressions of EMT-related proteins (ZEB1, Vimentin and E-cadherin). aP < 0.05 vs control.
- Citation: Shan KS, Li WW, Ren W, Kong S, Peng LP, Zhuo HQ, Tian SB. LncRNA cancer susceptibility 20 regulates the metastasis of human gastric cancer cells via the miR-143-5p/MEMO1 molecular axis. World J Gastroenterol 2022; 28(16): 1656-1670
- URL: https://www.wjgnet.com/1007-9327/full/v28/i16/1656.htm
- DOI: https://dx.doi.org/10.3748/wjg.v28.i16.1656