Department of Epidemiology, Unit 1340, The University of Texas M. D. Anderson Cancer Center, 1155 Pressler Blvd., Houston, TX 77030, USA.
Urol Oncol. 2012 Jul-Aug;30(4):524-32. doi: 10.1016/j.urolonc.2012.04.003.
Urinary bladder cancer is a heterogeneous disease with diverse genetic and environmental risk factors that can influence disease risk or clinical course for recurrence, progression, and survival. Therefore, identification of these factors is paramount for disease prevention and optimal clinical management of bladder cancer patients. Of particular interest is the need to identify molecular biomarkers that can give accurate assessment of tumor biological potential and to predict treatment response. Recent advances in molecular biology, cytogenetic, and genomic research have spurred discovery efforts for novel genetic, epigenetic, and proteomic biomarkers that are prognostic for cancer. This review focuses on some of the important germ line polymorphisms found to be correlated with clinical outcomes in bladder cancer. So far, most of the identified candidate loci were based on prior knowledge of pathogenesis and had not been validated for clinical applications. The future challenges are to analyze the wealth of information from whole-genome studies, to understand the underlying biological mechanisms of these associations, the network of gene-gene and gene-environment interactions, and to apply these markers for the identification of high-risk population for targeted, personalized therapy.
膀胱癌是一种具有异质性的疾病,存在多种遗传和环境风险因素,这些因素可能会影响疾病的复发、进展和生存风险或临床病程。因此,识别这些因素对于膀胱癌的疾病预防和最佳临床管理至关重要。特别需要确定能够准确评估肿瘤生物学潜力并预测治疗反应的分子生物标志物。分子生物学、细胞遗传学和基因组研究的最新进展推动了对新型遗传、表观遗传和蛋白质组学生物标志物的发现,这些标志物对癌症具有预后价值。本综述重点介绍了一些与膀胱癌临床结果相关的重要种系多态性。到目前为止,大多数已确定的候选基因座都是基于对发病机制的已有认识,尚未经过临床应用验证。未来的挑战是分析全基因组研究产生的大量信息,以了解这些关联的潜在生物学机制、基因-基因和基因-环境相互作用网络,并将这些标志物应用于高危人群的识别,以进行靶向、个体化治疗。