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. 2021 May 26;40:177. doi: 10.1186/s13046-021-01973-z

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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. 3 — DLX6-AS1 is overexpressed and triggers migration, invasion and EMT in HCC. a. RT-qPCR detection of DLX6-AS1 expression in cancer tissues and normal tissues, as well as cancer cells and normal liver cells; b. RT-qPCR detection of DLX6-AS1 expression in SMMC-7721 and HepG2 cells after up-regulating DLX6-AS1; c. Transwell assay tested the invasion and migration of SMMC-7721 cells after up-regulating DLX6-AS1; d. Transwell assay tested the invasion and migration of HepG2 cells after up-regulating DLX6-AS1; e. RT-qPCR analysis of E-cadherin, N-cadherin, vimentin and MMP7 mRNA expression in SMMC-7721 and HepG2 cells after up-regulating DLX6-AS1; data were expressed as mean ± standard deviation (repetition = 3) and evaluated by One-way AVONA and Tukey’s test. $ P < 0.05 compared with the HL-7702 cells; * P < 0.05 compared with the oe-NC group