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Updated: Jan 12, 2026
3-D Cell Culture System for Studying Invasion and Evaluating Therapeutics in Bladder Cancer
Published on: September 13, 2018
REV3L as a prognostic biomarker and therapeutic target in bladder urothelial carcinoma
Yangyang Pang1, Tiantian Liu1, Xin Wu1
1Department of Urology, Shanghai Xuhui Central Hospital, Zhongshan-Xuhui Hospital, Fudan University, Shanghai, 200031, China.
Background:
The functional significance and clinical relevance of the translesion DNA synthesis polymerase subunit REV3L in bladder urothelial carcinoma (BLCA) require comprehensive characterization.
Methods:
Bioinformatic analysis of TCGA and GEO datasets was integrated with extensive experimental validation. The expression of REV3L was evaluated across various stages of BLCA, and its correlation with patient survival was analyzed using Kaplan-Meier analysis and Cox regression modelling. Additionally, immune infiltration patterns and pathway enrichment levels were investigated using GSEA. The functional consequences of REV3L depletion (shRNA) were evaluated in UMUC3 and SW780 cells through a series of assays for proliferation, colony formation, glycolysis (lactate production, glucose uptake, and gene expression), and cisplatin sensitivity (CCK-8 and apoptosis).
Results:
REV3L expression was significantly lower in BLCA tumors than in normal tissues but higher in advanced-stage and high-grade tumors. High REV3L expression was found to be a strong predictor of poor overall survival, disease-specific survival, and progression-free interval. Furthermore, multivariate analysis revealed that high REV3L expression was an independent prognostic factor. The incorporation of REV3L into a nomogram enabled accurate prediction of patient survival. The present study demonstrated a positive correlation between REV3L and effector memory T cells, Th1 cells, and Th17 cells, and a negative correlation with NK CD56bright cells. REV3L-high tumors exhibited enrichment in glycolysis, DNA repair, G2M checkpoint, mitotic spindle, inflammatory response, and MYC target pathways. Silencing REV3L led to the suppression of proliferation, colony formation, lactate production, and glucose uptake, alteration of glycolytic gene expression, and enhancement of cisplatin-induced apoptosis.
Conclusions:
The present findings establish a pivotal, context-dependent role for REV3L in BLCA, which is implicated in tumor initiation suppression and aggressive progression promotion through metabolic reprogramming, immune modulation, and therapy resistance. It is evident that REV3L functions as both a robust independent prognostic biomarker and a compelling therapeutic target for BLCA.
