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. 2020 Oct 29;39:229. doi: 10.1186/s13046-020-01748-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. 7 — UPK1A-AS1 functions through EZH2. a-b. Expression of the indicated genes were monitored by qRT-PCR after co-transfection of UPK1A-AS1 vectors and si-EZH2 into SK-Hep-1 (a) and MHCC-97H (b) cells (^*P < 0.05, ^**P < 0.01, ^***P < 0.001). c. Expression of the indicated proteins was measured by western blotting after co-transfection of UPK1A-AS1 vectors and si-EZH2 into SK-Hep-1 and MHCC-97H cells. d-g. Effect of co-transfection of UPK1A-AS1 vectors and si-EZH2 on the cell proliferation of SK-Hep-1 (d-e) and MHCC-97H (f-g) cells, as measured by the EdU assay (^**P < 0.01, ^***P < 0.001)