Hegazi Mohamed A A A, Pasqualini Fabio, Chiriva-Internati Maurizio, Taverna Gianluigi, Grizzi Fabio
Department of Immunology and Inflammation, IRCCS Humanitas Research Hospital, Rozzano, Milan 20089, Italy.
Departments of Gastroenterology, Hepatology and Nutrition, Division of Internal Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, United States.
Bladder (San Franc). 2025 Apr 11;12(2):e21200039. doi: 10.14440/bladder.2024.0071. eCollection 2025.
Bladder cancer (BLCA) remains a prevalent and complex malignancy characterized by significant heterogeneity. Treatment strategies are diverse, based on patient characteristics and cancer stage. Early identification of biomarkers is crucial for improving diagnosis, staging, and treatment planning. These biomarkers offer valuable insights into lesion features, tumor differentiation, and disease progression, thereby playing a pivotal role in the personalized management of BLCA.
This study investigated the expression of cancer-testis antigens and in BLCA using comprehensive bioinformatic analyses to assess their potential as biomarkers.
The UALCAN database, based on The Cancer Genome Atlas datasets, was employed to compare and expression levels in normal bladder tissues and BLCA samples. In addition, the Kaplan-Meier Plotter, OncoDB, and TIMER 2.0 platforms were utilized to evaluate the prognostic and immunotherapeutic relevance of these antigens.
The findings suggest that and are integral to various biological processes driving BLCA onset and progression. Both genes appear to facilitate BLCA cell progression and migration, contributing to poor prognosis through specific pathways and by altering tumor microenvironment. Notably, expression was significantly upregulated in BLCA tissues compared to normal tissues. Conversely, higher expression was associated with longer overall survival and positively correlated with immunotherapeutic targets.
Although these results were derived from analyses, they offer insights into the potential roles of and as biomarkers. Further studies are warranted to validate these biomarkers in retrospective patient cohorts to establish their clinical utility.
膀胱癌(BLCA)仍然是一种普遍且复杂的恶性肿瘤,具有显著的异质性。治疗策略因患者特征和癌症分期而异。早期识别生物标志物对于改善诊断、分期和治疗规划至关重要。这些生物标志物为病变特征、肿瘤分化和疾病进展提供了有价值的见解,从而在BLCA的个性化管理中发挥关键作用。
本研究使用综合生物信息学分析调查了癌症-睾丸抗原在BLCA中的表达,以评估它们作为生物标志物的潜力。
基于癌症基因组图谱数据集的UALCAN数据库用于比较正常膀胱组织和BLCA样本中的表达水平。此外,还利用了Kaplan-Meier Plotter、OncoDB和TIMER 2.0平台来评估这些抗原的预后和免疫治疗相关性。
研究结果表明,对于驱动BLCA发病和进展的各种生物学过程至关重要。这两个基因似乎都促进了BLCA细胞的进展和迁移,通过特定途径并改变肿瘤微环境导致预后不良。值得注意的是,与正常组织相比,BLCA组织中的表达显著上调。相反,较高的表达与更长的总生存期相关,并且与免疫治疗靶点呈正相关。
尽管这些结果来自分析,但它们为作为生物标志物的潜在作用提供了见解。有必要进行进一步的研究,在回顾性患者队列中验证这些生物标志物,以确定它们的临床效用。