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. 2021 Sep 20;7:255. doi: 10.1038/s41420-021-00649-z

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© The Author(s) 2021

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. 3 — A KEGG pathway analysis for DLGAP1-AS2 co-expressed genes from TCGA dataset. B TOP flash/FOP flash assays in AGS and HGC-27 cells upon DLGAP1-AS2 knockdown. C RT-qPCR assays for the expression of Wnt1 and its downstream targets upon DLGAP1-AS2 knockdown. D Western blot analysis of the main factors related to Wnt/β-catenin signaling upon DLGAP1-AS2 knockdown. The data shown are representative of three independent experiments. E-Cad E-cadherin, N-Cad N-cadherin. *P < 0.05.