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. 2021 Aug 28;21:277. doi: 10.1186/s12890-021-01633-0

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© The Author(s) 2021

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. 2 — DLGAP1-AS2 and miR-503 directly interacted with each other. The interaction between DLGAP1-AS2 and miR-503 was predicted by IntaRNA 2.0 (A). For dual-luciferase reporter assay, DLGAP1-AS2 luciferase vector + miR-503 mimic (miR-503 group) or DLGAP1-AS2 luciferase vector + NC miRNA (NC group) was co-transfected into H2170 cells using Lipofectamine 2000. Luciferase activity was measured at 48 h of post-transfection (B)