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. 2020 Mar 2;39(17):3541–3554. doi: 10.1038/s41388-020-1237-0

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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. 4 — a Venn diagram shows the number of differentially expressed genes (DEGs) between MCT-SCC and each SCC using TCC based on an FDR q value < 0.05. b Box plots show log2 TPM of XCL1 in different types of SCCs, ASCs, and ACs. c Dot plots show relative XCL1 expression among MCT-SCC/ASC (n = 5), cervix SCC (n = 21), and ovarian HGSC (n = 17) samples by using real-time RT-PCR. d Dot plots show XCL1 expression of MCT-SCC/ASC (n = 24), ovarian HGSC (n = 19), and benign MCT (n = 8) samples evaluated by using immunohistochemistry. The H score was obtained by the following formula: 3 × percentage of strongly stained cytoplasm + 2 × percentage of moderately stained cytoplasm + percentage of weakly stained cytoplasm, giving a range of 0–300. The dotted line indicates the lower cutoff value for a positive result (H score = 20).