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. 2021 Oct 30;7:328. doi: 10.1038/s41420-021-00722-7

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© The Author(s) 2021, corrected publication 2022

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Fig. 6 — A–C CoIP assay showed the association between exogenous FBXL10 with HDAC1 and HDAC2. D CoIP assay showed the endogenous protein interaction between FBXL10 and HDAC1. E. Immunofluorescence assay showed the colocalization of FBXL10 (red) and HDAC1 (green) in MCF7 cells. F CoIP assay showed the effect of FBXL10 overexpression on the interaction between SNAI1 and HDAC1. G CoIP assay showed the effect of FBXL10 on HDAC1-mediated deacetylation of exogenous SNAI1. H CoIP assay showed the effect of overexpression FBXL10 on endogenous SNAI1 acetylation. I Reporter gene assay assessed the effect of FBXL10/SNAI1/HDAC1 on the E-cadherin luciferase activity. J Transwell assay was performed to evaluate the effect of FBXL10 and HDAC1 inhibitor MS-275(1 μM for 12 h) on the migration and invasion of MCF7 cells.