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. 2020 Jan 3;20:3. doi: 10.1186/s12935-019-1078-5

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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 — Suppression of UBQLN4 inhibits tumor formation ability of HCC cells in vivo. a–c The in vivo effect of UBQLN4 was evaluated in xenograft mouse models bearing tumors originating from SMMC-7721 cells via tumor volume and photon flux; n = 6 per group. d–f Expression of UBQLN4 and Ki67 were detected between UBQLN4 shRNA and negative control groups in node mouse tumor tissues. *p < 0.05, **p < 0.01