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. 2020 Jul 9;11(7):521. doi: 10.1038/s41419-020-02740-2

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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. 2 — a qRT-PCR analysis of CCDC144NL-AS1 mRNA in SGC7901 and BGC823 cells treated with si-CCDC144NL-AS1. b, c CCK-8 assay was applied to detect cell viability. d–g Colony formation assays and the Edu assays were conducted to measure cell proliferation ability in BGC823 and SGC7901 cells (scale bar: 100 μm for Edu assay). h–n Representative results of transwell assays and wound healing assays of GC cells after si-CCDC144NL-AS1 transfection (scale bar: 200 μm for transwell assay, 100 μm for wound healing assay). **p < 0.01, ***p < 0.001.