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. 2020 Jun 8;20:163. doi: 10.1186/s12890-020-1174-2

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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. 2 — MIR205HG was an upstream factor for miR-299-3p in LUSC. a. The potential miRNA expression in LUSC was downloaded from dbDEMC 2 website. b. RIP assay was applied to confirm the relationship between MIR205HG and miR-299-3p. c. StarBase database was used to predict the potential binding sites between MIR205HG and miR-299-3p. d. Luciferase reporter assay was carried out to verify that MIR205HG could bind with miR-299-3p. e. qRT-PCR analysis was performed to assess the relative expression of miR-299-3p in both cell lines transfected with sh-MIR205HG#1. All data were showed as the mean ± SD. **P < 0.01