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. 2019 Jan 10;10(1):32. doi: 10.1038/s41419-018-1262-x

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© The Author(s) 2018

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 3 — a and b Cell migration and Matrigel invasion assays was used to examine the effects of miR-1254 on GC cell migration and invasion, the migration and invasion capability were quantified as cell numbers (scale bar: 200 μm). c Wound healing was performed to determine the ability of cell migration after transfected with miR-1254-mimics and miR-1254-inhibitor, the migratory rate was calculated by migration distance/original width (scale bar: 100 μm). *p < 0.05; **p < 0.01; ***p < 0.001. The data expressed as the mean ± SD