Comprehensive analysis of coagulation-associated gene signature in bladder cancer diagnosis, prognosis, and immunotherapy

In recent years, research on the relationship between coagulation system abnormalities and tumor immunity has been widely reported. Bladder cancer (BC), as an immunogenic tumor, holds great promise in immunotherapy. The role of coagulation-related genes in predicting the prognosis of BC patients and the efficacy of immunotherapy remains to be explored. In this study, we utilized the TCGA data system to analyze the biological functions of coagulation-related genes (CRGs) in BC patients. Additionally, we employed multiple machine learning methods (LASSO regression, SVM-RFE regression, and random forest) to establish diagnostic and prognostic signatures for BC based on CRGs. Univariate and multivariate Cox analyses indicated that the prognostic signature is an independent risk factor. Combining risk scores and independent clinical parameters, we established a Nomogram with a C-index of 0.812. Furthermore, we applied CRGs to cluster BC patients, and significant differences were observed between the two clusters in terms of immune cell infiltration, immune cell pathway activity, and response to immunotherapy. In conclusion, we systematically analyzed the value of CRGs in the diagnosis, prognosis, and personalized treatment of BC patients.

Authors

Institutions

Publication Details

Journal
Scientific Reports
Published
2025-10-29
DOI
https://doi.org/10.1038/s41598-025-17567-0
Primary Topic
Ferroptosis and cancer prognosis
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Comprehensive analysis of coagulation-associated gene signature in bladder cancer diagnosis, prognosis, and immunotherapy

Wei E. I. Sha, Guicao Yin, Shengqi Zheng, Tian Hua et al.
Scientific Reports
Ferroptosis and cancer prognosis
article

Comprehensive analysis of coagulation-associated gene signature in bladder cancer diagnosis, prognosis, and immunotherapy

Wei E. I. Sha, Guicao Yin, Shengqi Zheng, Tian Hua, Jialong Wang, Xiang Pan, Yifan Li, Wei Zhang
article en

Abstract

In recent years, research on the relationship between coagulation system abnormalities and tumor immunity has been widely reported. Bladder cancer (BC), as an immunogenic tumor, holds great promise in immunotherapy. The role of coagulation-related genes in predicting the prognosis of BC patients and the efficacy of immunotherapy remains to be explored. In this study, we utilized the TCGA data system to analyze the biological functions of coagulation-related genes (CRGs) in BC patients. Additionally, we employed multiple machine learning methods (LASSO regression, SVM-RFE regression, and random forest) to establish diagnostic and prognostic signatures for BC based on CRGs. Univariate and multivariate Cox analyses indicated that the prognostic signature is an independent risk factor. Combining risk scores and independent clinical parameters, we established a Nomogram with a C-index of 0.812. Furthermore, we applied CRGs to cluster BC patients, and significant differences were observed between the two clusters in terms of immune cell infiltration, immune cell pathway activity, and response to immunotherapy. In conclusion, we systematically analyzed the value of CRGs in the diagnosis, prognosis, and personalized treatment of BC patients.

Scientific ReportsVol. 15(1)
Jiangsu University (CN), Huaian First People’s Hospital (CN), General Hospital of Shenyang Military Region (CN), Yangzhou University (CN)
Yangzhou University
Openalex Percentile: Top 55%
Ferroptosis and cancer prognosis
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.