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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. 2 — a CCK-8 assay was used to explore the proliferation of GC cells transfected with miR-1254-mimics and miR-1254-inhibitor lentivirus. b Effects of miR-1254 difference on the colony formation of GC cells. c EDU incorporation assay was used to examine the effect of miR-1254 on proliferation in MGC803 cells transfected with the miR-1254 mimics and SGC7901 transfected with the miR-1254 inhibitor (scale bar: 200 μm). d Effects of miR-1254 difference on cell cycle distribution of GC cells. *p < 0.05; **p < 0.01; ***p < 0.001. The data expressed as the mean ± SD