Strategies for molecular expression profiling in bladder cancer

被引:28
|
作者
Mitra, Anirban P. [2 ]
Bartsch, Claudia C. [3 ,4 ]
Cote, Richard J. [1 ]
机构
[1] Univ Miami, Miller Sch Med, Dept Pathol, Miami, FL 33136 USA
[2] Univ So Calif, Keck Sch Med, Dept Pathol, Los Angeles, CA 90033 USA
[3] Univ So Calif, Keck Sch Med, Dept Urol, Los Angeles, CA 90033 USA
[4] Univ Ulm, Dept Urol, Ulm, Germany
关键词
Transitional cell carcinoma; Cell-cycle regulation; Apoptosis; Signal transduction; Angiogenesis; Gene expression profiling; Prognosis; TRANSITIONAL-CELL CARCINOMA; ENDOTHELIAL GROWTH-FACTOR; GENE-EXPRESSION; URINARY-BLADDER; TUMOR PROGRESSION; NEOADJUVANT CHEMOTHERAPY; DISEASE PROGRESSION; RADICAL CYSTECTOMY; PROGNOSTIC FACTOR; P53; ALTERATIONS;
D O I
10.1007/s10555-009-9196-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Carcinoma of the urinary bladder involves alterations in multiple cellular pathways that dictate the pathology of the disease and clinical outcome of the patient. This includes alterations in regulation of the cell cycle, apoptotic mechanisms, signal transduction and tumor angiogenesis. Interrogation of alterations in multiple molecules associated with these pathways is leading to the development of biomarker panels that are capable of predicting an individual patient's outcome or response to specific treatments. With respect to gene expression profiling, two broad approaches may be identified: a global approach and a pathway-specific approach. The global approach involves a high-throughput effort to profile the entire genome, while the pathway-specific approach quantifies select genes across several pathways. While the former has a high potential for discovery of novel signatures, the latter is important in generating reproducible and concise panels that have the potential for rapid clinical implementation. A combination of both these approaches is needed for the identification and validation of robust marker panels of potential clinical importance in bladder cancer.
引用
收藏
页码:317 / 326
页数:10
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