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. 2024 Aug 9;14:18500. doi: 10.1038/s41598-024-68859-w

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© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, 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 you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. 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-nc-nd/4.0/.

PMC Copyright notice

PPlncPS construction in bladder cancer. The results of the TCGA-BLCA cohort were presented in the left column, and the results of the E-MTAB-4321 cohort were presented in the right column. (a) Kaplan–Meier curve revealed that the patients in the low-PPlncPS score group had a better prognosis than those in the high-PPlncPS score group (p < 0.001, p = 0.008). (b) The heatmap showed that the expression patterns of LINC00174, HCP5, HCG27, UCA1, SNHG15, GHRLOS, CYB561D2, and AGAP11 between the two groups were different in both cohorts. (c,d) Distribution of patients in the TCGA-BLCA cohort and E-MTAB-4321 cohort and survival information of each patient. PPlncPS: pan-PCD-related lncRNA prognostic signature.