Correction to: Scientific Reports https://doi.org/10.1038/s41598-024-70752-5, published online 28 August 2024
The original version of this Article contained errors in Figure 7. In panel 7B, the image of panel ‘scrambled shRNA’ was a duplication of panel image 2A, ‘scrambled shRNA’. Additionally, in Figure 7C the images of ‘scrambled shRNA’ were duplicated from the ‘emerin shRNA’ panel images.
The original Figure 7 and accompanying legend appear below.
Reducing emerin in MDA-231 cells increases their impeded migration. (A) A violin plot of the number of cells migrating through 8 µm trans-well pores is shown for MDA-231, control shRNA, emerin shRNA, and scrambled shRNA MDA-231 cell lines (N = 5 fields). The mean is depicted as the dark dashed line and the thin dashed lines represent the first and third quartiles. *P < 0.0037 compared to control shRNA, one-way ANOVA followed by Dunnett’s multiple comparison; 3 biological replicates were used for each cell line. (B) Representative DAPI images of the cells that successfully migrated in the trans-well assays in A. (C) Scratch-wound healing assay. MDA-231, control shRNA, emerin shRNA, and scrambled shRNA MDA-231 cell lines were plated, scratched with a pipette tip, and migration into the wound area was monitored every 2 h for 8 h. Representative phase images are shown. (D) The rate of scratch wound healing, which refers to the ability of cells to migrate into the wound area, is shown with SEM. Two-way ANOVA was used, and no significant differences were seen.
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Hansen, E., Rolling, C., Wang, M. et al. Correction: Emerin deficiency drives MCF7 cells to an invasive phenotype. Sci Rep 15, 27632 (2025). https://doi.org/10.1038/s41598-025-13048-6
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DOI: https://doi.org/10.1038/s41598-025-13048-6
