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. 2018 Sep 19;18:144. doi: 10.1186/s12935-018-0639-3

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© The Author(s) 2018

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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.

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Fig. 5 — Effect of knockdown of RIG-I on cellular functions of gastric cancer cell lines. a Knockdown of RIG-I in SGC-7901 cells could increase the cell viability at 48 h and 72 h post-transfection (both P < 0.001). b Knockdown of RIG-I in AGS cells could increase the cell viability at 48 h and 72 h post-transfection (P < 0.01 and P < 0.05, respectively). c Knockdown of RIG-I significantly increased the cell migration ability in SGC-7901 cells at 24 h after scraping (P < 0.01). d Knockdown of RIG-I could increase the cell migration ability in AGS cells at 24 h after scraping (P < 0.01). e The number of crystal violet-stained cells was significantly increased after RIG-I knockdown expression in both two cell lines (P < 0.05), respectively. f The ratio of gastric cells in G2/M phase was significantly increased in after RIG-I knockdown expression in both SGC-7901 and AGS cells (P < 0.05 and P < 0.01, respectively)