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. 2021 Apr 30;40:148. doi: 10.1186/s13046-021-01943-5

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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. 7 — BBOX1-AS1 facilitates the malignant progression of NSCLC by regulating MELK expression. a-e A549 and SK-MES-1 cells were transfected with si-NC, si-BBOX1-AS1#2 or si-BBOX1-AS1#2 + MELK. a CCK-8 assays were used to determine cell viability. b Colony formation assays in transfected cells. c Wound healing assays were performed to measure cell migration capability. d Transwell assays were utilized to detect cell invasion ability. e Western blot assays were conducted to exaine the protein levels of E-cadherin, N-cadherin and vimentin. **P < 0.01, ***P < 0.001