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. 2022 Oct 12;149(8):4701–4717. doi: 10.1007/s00432-022-04391-6

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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/.

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Fig. 3 — Proteomic analysis of CRPC and control urine-derived EV. A Venn diagram of the number of proteins identified in CRPC and control urine-derived EV. B Cellular component, C biological process, and D molecular function enrichment analyses of urine-derived EV proteins that are exclusive to the CRPC (n = 9) and control (n = 3) samples. Visualisation of cellular components is limited to CRPC urine-derived EV proteins since only one GO term was enriched for control urine-derived EV proteins (endoplasmic reticulum lumen, p-value = 0.0049, adjusted p-value = 0.088). GO terms enriched by 7 urine-derived EV proteins exclusive to controls were selected based on the significance level of adjusted p-value < 0.1