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. 2017 Sep 8;7:11000. doi: 10.1038/s41598-017-11374-y

Figure 5.

Figure 5

MIER3 is associated with Sp1 and promotes EMT in CRC cells. (A) MIER3 co-immunoprecipitates with Sp1 in CRC cells. Lysates from SW620 cells were immunoprecipitated with MIER3 antibody or control IgG and detected with Sp1 antibody on a western blot and then immunoprecipitated with Sp1 antibody or control IgG and detected with MIER3 antibody on a western blot. (B) The spindle cell phenotype of SW620/shMIE3 cells and the epithelial phenotype of CRC cells from the SW620/shNC control group showing epithelial-to-mesenchymal transition (EMT) induced by decreased MIER3 expression. (C) MIER3 knockdown led to increased Sp1 expression and induced hallmarks of EMT, including decreased E-cadherin and ZO-1 and the accumulation of vimentin and N-cadherin in CRC cells. In contrast, down-regulation of Sp1 led to decreased E-cadherin and ZO-1 expression and increased vimentin and N-cadherin expression. (D) MIER3 overexpression led to decreased Sp1 expression and induced the accumulation of E-cadherin, ZO-1 and the decreased expression of vimentin, and N-cadherin in CRC cells. While up-regulation of Sp1 led to increased E-cadherin and ZO-1, it inhibited vimentin and N-cadherin expression. Error bars represent the mean ± SD.