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. 2022 Jan 4;22:3. doi: 10.1186/s12935-021-02423-8

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© The Author(s) 2021

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 — B7H4-high predicts proliferative subtype and limited therapeutic options in CeCa. A Differences in enrichment scores of several therapeutic signatures in B7H4-high, PDL1-high and co-low subgroups. B Differences in Ki67 expression B7H4-high, PDL1-high and co-low subgroups. C Differences in the drug-target genes expression in B7H4-high, PDL1-high and co-low subgroups. D Differences in EGFR expression in B7H4-high, PDL1-high and co-low subgroups. E Differences in IC50 of common anti-cancer drugs in B7H4-high, PDL1-high and co-low subgroups. *P < 0.05; ***P < 0.001; ****P < 0.0001