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. 2020 Aug 7;9(19):7218–7230. doi: 10.1002/cam4.3313

Figure 8.

Figure 8

The accumulation of miR‐520a‐3p reverses the effects of exosomal LIMK1 on HCC cells. MHCC97‐H and HCCLM3 cells were treated with Huh7‐exo, Propofol‐Huh7‐exo, Vector‐Propofol‐Huh7‐exo, Over LIMK1‐Propofol‐Huh7‐exo, Over LIMK1‐Propofol‐Huh7‐exo + mimic NC or Over LIMK1‐Propofol‐Huh7‐exo + miR‐520a‐3p mimic. (A) MTT assay was conducted to detect the proliferation of HCC cells. (B) Flow cytometry was used to detect the apoptosis rate of HCC cells. (C and D) Transwell assays were performed to examine the metastasis of HCC cells. (E) The enrichment of metastasis‐related proteins in HCC cells was examined by Western blot assay. *P < .05