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. 2023 Nov 14;7:120. doi: 10.1038/s41698-023-00471-z

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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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 3 — a The percentage of PCM (blue, n = 332), MBM (orange, n = 86), and ECM (gray, n = 801) with PTEN mutations. Chi-square test; **p < 0.005. b ssGSEA analysis for normalized enrichment scores (NES) of hallmark angiogenesis pathway comparing tumors with PTEN mutations (green) and without PTEN mutations (gray) within PCM, MBM, and ECM groups. Black line indicates median. Mann-Whitney test; *p < 0.05. c The mRNA levels of key regulatory genes (STAT3, VEGFA, AKT1, PIK3CA, and CCL2) in the angiogenesis pathway were cross compared between MBM tumors with PTEN mutations (green) and without PTEN mutations (gray). Black line indicates median. Mann-Whitney test; *p < 0.05.