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. 2023 Nov 27;21:860. doi: 10.1186/s12967-023-04747-7

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© The Author(s) 2023

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 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 — Tissue metabolites as biomarkers to differentiate between subtype A and subtype B. Box plots showing relative abundances for the 7 metabolite-panel to distinguish PC subtypes A and B in addition with data from subtype non-AB and benign prostate tissues. Data are expressed as means ± standard deviation and statistical significance was determined using the one-way ANOVA followed by post-hoc Benjamini-Hochberg (FDR, false discovery rate) test and a p-value < 0.05 was considered statistically significant. PC + GPC—peak for combined phosphocholine/glycerophosphocholine metabolites; Glx: combined signal of glutamate/glutamine