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. 2020 May 7;11(5):336. doi: 10.1038/s41419-020-2518-9

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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 — a Immunohistochemistry staining of MUC15 in normal kidney tissues (n = 17) and RCC tissues (n = 40). The scale bar is 50 μm. b MUC15 mRNA expression in normal kidney tissues (n = 72) and RCC tissues (n = 315) from TCGA database. c MUC15 mRNA expression in 72 paired normal kidney and RCC tissues. d MUC15 mRNA expression in matched normal kidney and RCC tissues (n = 10) from GEO database (GSE6344). e MUC15 mRNA expression in not matched normal kidney (n = 8) and RCC tissues (n = 9) from GEO database (GSE781). f Western blot analysis of MUC15 protein expression level in human normal and renal cancer tissues, the quantification analysis was shown below. β-actin was used as a loading control (N = 3).