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. 2022 Oct 4;22:1037. doi: 10.1186/s12885-022-10122-4

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© The Author(s) 2022

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. 6 — Analysis of the difference in immunotherapy in FA metabolism-related lncRNA subgroups. A, B The boxplots display the immune checkpoints that were up-regulated in C1 compared with C2 in the TCGA and GSE76427 cohorts. C Differences in the TIDE score and immune response status of the different molecular subtypes in the TCGA cohort. D Differences in the TIDE score and immune response status of the different molecular subtypes in the GSE76427 cohort. Abbreviations: FA, Fatty acid; lncRNA, Long non-coding RNA; TCGA, The Cancer Genome Atlas; TIDE, Tumor Immune dysfunction and exclusion