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. 2020 Dec 9;39:277. doi: 10.1186/s13046-020-01780-y

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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. 5 — Reduced expression of MYLK-AS1 decreases the proliferation, migration and invasion of HCC cells. a Relative MYLK-AS1 expression in Hep-G2 and MHCC-97H cells transfected with two independent shRNAs targeting MYLK-AS1 by qRT-PCR. b-c Hep-G2 and MHCC-97H cell proliferation after knockdown of MYLK-AS1 by CCK-8 assay. d-h Representative results of the colony formation (scale bar = 500 μm), cell cycle assay, apoptosis assays, and transwell assay (scale bar = 100 μm), in Hep-G2 and MHCC-97H cells after shMYLK-AS1–1 or shMYLK-AS1–2 transfection. Results are expressed as mean ± SD. *P < 0.05, **P < 0.01, and ***P < 0.001