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. 2020 Apr 20;11(4):248. doi: 10.1038/s41419-020-2471-7

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© The Author(s) 2020

Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 1 — Upregulated expression of SPR in HCC tissue compared to paired nontumor tissues in a TCGA (n = 374) and b GSE102079 (n = 152) datasets. c and d The expression level of SPR was consistently analyzed in human liver and HCC specimens. Scale bar: 50 μm. e Kaplan–Meier survival analysis of the prognostic value of SPR based on the expression data of HCC patients (n = 97). f Multivariate Cox regression analysis of clinicopathological factors for overall survival in the HCC patients (n = 97). CI confidence interval, HR hazard ratio, NT nontumor tissues.