High FSTL1 expression promotes bladder cancer progression by enhancing tumor cell migration
摘要
Emerging evidence highlights diverse roles of FSTL1 across various malignancies, though its biological significance in bladder carcinogenesis remains unexplored.
MethodsThis study systematically interrogated FSTL1 using multidimensional bioinformatics approaches—including tumor microenvironment characterization, survival pattern evaluation, and differential expression profiling—through multiple bladder cancer datasets from TCGA and GEO repositories, with subsequent experimental validation employing in vitro cellular models.
ResultsOur findings demonstrate that FSTL1 exhibits significant overexpression in bladder tumors, promotes cancer cell motility through pro-migratory mechanisms, and potentially modulates key components of the tumor microenvironment.
ConclusionFSTL1 might be a therapeutic target or biomarker for the advancement of bladder cancer.