Cancer Med. 2026 Jul;15(7):e72025. doi: 10.1002/cam4.72025.
ABSTRACT
BACKGROUND: Clinical and epidemiological evidence has suggested a potential association between kidney dysfunction and bladder cancer (BC). One hypothesis for this comorbidity is the presence of a common genetic etiology. However, little is known about the shared genetics and causality of this association. Thus, we aimed to investigate shared genetic architecture and the causal link between kidney dysfunction and bladder cancer.
METHODS: Leveraging summary statistics from large-scale genome-wide association studies (GWASs) conducted on European-ancestry populations on eGFRcrea (N = 1,004,040), eGFRcys (N = 460,826), BUN (N = 852,678), UACR (N = 288,649), urate (N = 547,361) and BC (N cases = 3357, N controls = 628,027), we conducted a large-scale genome-wide cross-trait study to determine genetic overlap, to identify shared loci, and to infer causal relationships. We evaluated genetic correlation through linkage disequilibrium score regression (LDSC). Integration of single-trait GWAS was accomplished by multi-trait analysis of GWAS (MTAG), which enabled cross-trait meta-analysis to unveil overlapping genetic loci between five kidney function traits and BC. Shared genes were further validated through colocalization analysis and transcriptome-wide association analysis. Bidirectional Mendelian Randomization (MR) was conducted to determine causal inference of kidney function traits on BC.
RESULTS: We found positive correlations between both BUN and urate and BC at the genome-wide level. A total of 157 significant overlapping genetic loci (range 7 to 72) were identified across five kidney function traits and BC. Among them, PSCA was prioritized as the strongest shared gene with support from MTAG, colocalization, and TWAS, whereas ZFHX3, TTC33, and ATP2A1 were considered candidates supported only by MTAG and TWAS. MR provided the most consistent support for a potential positive causal effect of BUN on BC, limited support for UACR, and exploratory evidence for urate.
CONCLUSIONS: Our cross-trait analysis demonstrated a shared genetic basis underlying kidney function and BC, providing novel insights into the biological functions and molecular mechanisms underlying these complex traits.
PMID:42470241 | DOI:10.1002/cam4.72025
