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. 2020 Aug 3;39:149. doi: 10.1186/s13046-020-01648-1

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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 — Circ-CPA4 inhibited let-7 miRNA expressions in NSCLC cells by acting as a RNA sponge. a The binding sites of circ-CPA4 and let-7 miRNA were predicted by using the online starBase software (http://starbase.sysu.edu.cn/). Dual-luciferase reporter gene system assay was performed to validate the binding sites of circ-CPA4 and let-7 miRNA in b A549, c H1299, d SK-MES-1 and e Calu-3 cells, respectively. Let-7 miRNA enriched in the pull-down production with the circ-CPA4 probe in f A549, g H1299, h SK-MES-1 and i Calu-3 cells, respectively. Each experiment repeated at least 3 times. *P < 0.05, **P < 0.01, NS means no statistical significance