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. 2022 Sep 8;41:270. doi: 10.1186/s13046-022-02478-z

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© The Author(s) 2022

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 — LINC01132 increases cancer cell growth, proliferation, invasion and metastasis in vitro. A Colony formation assays of the effects of siLINC01132 vs. controls. B Colony formation assays of the effects of overexpression of LINC01132 vs. controls. C-D Cell Counting Kit-8 (CCK-8) assays showing the growth of HCC cells treated with siLINC01132 (C) or overexpression of LINC01132 (D). E-G Transwell migration and invasion assays in HCC cell lines treated with siLINC01132 or overexpression of LINC01132. E for migration treated with siLINC01132, F for invasion treated with siLINC01132 and G for migration and invasion treated with overexpression of LINC01132