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. 2020 Jun 16;10:80. doi: 10.1186/s13578-020-00439-7

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© The Author(s) 2020

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 4 — Effect of miR-320d on cell proliferation and invasion abilities in GCA cell lines. Up-regulated miR-320d inhibited the proliferation of OE-19 cells by CCK-8 assay (a) and colony formation assay (c). Down-regulated miR-320d promoted the proliferation of SK-GT2 cells by CCK-8 assay (b) and colony formation assay (d). Up-regulated miR-320d inhibited the invasion ability of OE-19 cell by transwell assay (e) and wound healing assay (f). The * represents significant difference from miR-320d vector-transfected cells to EV-transfected cells (*: P < 0.05; **: P < 0.01; ***: P < 0.001). Data are shown as mean ± SD