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. 2017 Nov 10;39(1):101–108. doi: 10.3892/or.2017.6091

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Copyright: © Kou et al.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

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Figure 2. — HMGA2 regulates the metastatic phenotype of renal cell carcinoma cells. The ability of cell migration was evaluated by wound healing assay, and is expressed as the number of migrated cells. Representative photographs and statistical charts are shown for the HMGA2-knockdown ACHN (A) and HMGA2-overexpressing 786-O (B) cells compared with their corresponding control, respectively. Quantification from three independent experiments is shown with error bars representing standard deviation (SD). **P<0.01 and ****P<0.0001. Transwell migration and Matrigel invasion assays were used for the analysis of the migrated or invaded cells in the ACHN cells with HGMA2 knockdown (C) and 786-O with HMGA2 overexpression (D), respectively. Quantification from three independent experiments is shown with error bars representing standard deviation (SD). ***P<0.001 and ****P<0.0001.