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. 2020 Jun 12;20:234. doi: 10.1186/s12935-020-01311-x

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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. 4 — UBE2I expression in HCC based on nodal metastasis status, individual cancer stage or tumor grade. a The expression level of UBE2I in HCC samples compared with normal liver samples determined by Oncomine database. b UBE2I expression in HCC based on nodal metastasis status. c UBE2I expression in HCC based on individual cancer stage. d UBE2I expression in HCC based on tumor grade. e UBE2I protein expression levels in HCC cancer tissue and normal tissue were analyzed using immunohistochemical staining from HumanProteinAtlas database. P-value < 0.05 was considered as statistically significant