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. 2020 Jul 23;11(7):559. doi: 10.1038/s41419-020-02766-6

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© The Author(s) 2020

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. 5 — a CCK-8 to detect the proliferation of MGC-803 that transfected miR-628-p mimic or negative control. b The cell cycle of cells in a are detected by flow cytometry. c, d The colony formation of cells in a and the clone number was counted. e Detect the proliferation of AGS that transfected miR-628-p inhibitor or negative control. f The cell cycle of cells in e are detected by flow cytometry. g, h The colony formation of cells in e and the clone number was counted. i, j Transwell test to detect the migration and invasion of treated HGC-27. The migrated and invaded cells were counted. k, l Transwell test to detect the migration and invasion of treated AGS. The migrated and invaded cells were counted. m The protein expression of PIN1 downstreams after intervened miR-628-5p in MGC-803 and AGS. The data are shown as the mean ± s.d. (n = 3) in cell lines. **p < 0.01, ***p < 0.001. Scale bars: 200 μm.