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. 2023 Apr 19;14:1180404. doi: 10.3389/fendo.2023.1180404

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Copyright © 2023 Zhao, Wang, Ding, Ye, Cheng, Shao, Liu and Zhou

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Clinical, pathological, and biological characteristics of two DRG clusters. (A) All samples from the TCGA-BLCA, iMvigor210, and GSE13507 cohorts were divided into two clusters using a consensus clustering algorithm (k=2). (B) Cumulative Distribution Function (CDF) from k=2 to 9. (C) Kaplan-Meier curve shows different overall survival (OS) between the two DRG clusters. (D) Principal Component Analysis (PCA) shows significant differences between the two DRG clusters. (E) Heatmap shows differences in clinical information and DRG expression between the two DRG clusters. (F) Abundance of 23 infiltrating immune cells in the two DRG clusters. (G) GSVA of biological pathways between the two DRG clusters. ns, no significance,*p< 0.05, **p< 0.01, ***p< 0.001.