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. 2021 Dec 4;16:24. doi: 10.1186/s13062-021-00312-8

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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. 5 — LOXL1-AS1 exacerbates the malignant behaviors of HCC cells via miR-3614-5p/YY1. A, B Colony formation assay and EdU assay measured cell proliferation in different groups, specifically, sh/NC, sh/LOXL1-AS1#1, sh/LOXL1-AS1#1 + inhibitor and sh/LOXL1-AS1#1 + pcDNA3.1/YY1. C, D In addition to detection of mitochondrial membrane potential by JC-1 to reflect cell apoptosis, the apoptotic ability of cells was also evaluated via TUNEL assay in different groups. E, F Transwell assays estimated cell migration and invasion in different groups. **P < 0.01