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. 2017 Oct 13;38(6):3297–3308. doi: 10.3892/or.2017.6034

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Copyright: © Xie 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 4. — (A) Validation of FPR2 expression in FPR2-knockdown SKOV3 cells using RT-qPCR and Simple Western assays. The mRNA and protein levels of FPR2 were significantly decreased in the SKOV3^−shFPR2 cells compared with the control cells, with the SKOV3^−shFPR2-2 cells exhibiting the greatest inhibition. (B) The wound healing assay showed that FPR2 knockdown significantly decreased the cell migration rate at 4 h after scraping. Significantly different from the control (SKOV3^−shcontrol; *P<0.05). (C) The Transwell assay showed that FPR2 knockdown decreased the number of invasive SKOV3 cells (*P<0.05).