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. 2021 Sep 20;19:398. doi: 10.1186/s12967-021-03076-x

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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. 1 — Immune subtypes and gene programmes defining ER+/PR−/HER2− breast cancer. A Unsupervised clustering analysis of microarray data identified five immune subtypes. B Heatmap of gene programmes significantly enriched in ER+/PR−/HER2− breast cancer. Scores for gene programmes (GP scores) were defined as the average expression level of all genes in a particular module. In the heatmap, colors represent mean GP scores of each cluster and black dots denote modules showing highest significance for an individual subtype. C, D Kaplan–Meier analysis of patient survival stratified by cluster: C OS; D BCSS