TY - JOUR
T1 - Molecular biology of bladder cancer
T2 - Prognostic, and clinical implications
AU - Mirra, Anirban P.
AU - Lin, Henry
AU - Datar, Ram H.
AU - Cote, Richard J.
N1 - Funding Information:
The molecular studies of bladder cancer progression are funded by National Institutes of Health grants CA-65726, CA-70903, and CA-86871, and the p53-targeted therapy trial in bladder cancer is funded by National Cancer Institute grant CA-71921.
PY - 2006/6
Y1 - 2006/6
N2 - The role of various molecular determinants involved in the genesis, progression, and outcome of bladder cancer has been the focus of investigations for the past 2 decades. Increasingly, the analysis of the interplay between these molecular factors is taking center stage. We review herein the studies examining the effects of deregulation of the various molecules implicated in the cell cycle, apoptosis, and angiogenesis pathways and analyze the central role of p53 in regulating these pathways. Technological advancements enable detection and quantification of gene transcripts and protein products, helping us move toward achieving the goal of establishing diagnostic, prognostic, and therapeutic marker panels. Recent studies have therefore focused on multiple-marker analyses to generate informative panels that can have greater clinical value for bladder cancer management. The use of molecular marker panels can provide a more objective alternative to clinical parameters for diagnosis and treatment decisions. Clinical trials aimed at treating urothelial carcinoma based on a patient's molecular profile can be predicted to empower clinicians to personalize patient management through increased therapeutic efficacy.
AB - The role of various molecular determinants involved in the genesis, progression, and outcome of bladder cancer has been the focus of investigations for the past 2 decades. Increasingly, the analysis of the interplay between these molecular factors is taking center stage. We review herein the studies examining the effects of deregulation of the various molecules implicated in the cell cycle, apoptosis, and angiogenesis pathways and analyze the central role of p53 in regulating these pathways. Technological advancements enable detection and quantification of gene transcripts and protein products, helping us move toward achieving the goal of establishing diagnostic, prognostic, and therapeutic marker panels. Recent studies have therefore focused on multiple-marker analyses to generate informative panels that can have greater clinical value for bladder cancer management. The use of molecular marker panels can provide a more objective alternative to clinical parameters for diagnosis and treatment decisions. Clinical trials aimed at treating urothelial carcinoma based on a patient's molecular profile can be predicted to empower clinicians to personalize patient management through increased therapeutic efficacy.
KW - Angiogenesis
KW - Apoptosis
KW - Cell cycle
KW - Expression profiling
KW - Molecular pathways
KW - Multiple-marker analysis
KW - Prognostic markers
KW - Urothelial carcinoma
UR - http://www.scopus.com/inward/record.url?scp=33749053635&partnerID=8YFLogxK
U2 - 10.3816/CGC.2006.n.020
DO - 10.3816/CGC.2006.n.020
M3 - Article
C2 - 16859582
AN - SCOPUS:33749053635
SN - 1558-7673
VL - 5
SP - 67
EP - 77
JO - Clinical Genitourinary Cancer
JF - Clinical Genitourinary Cancer
IS - 1
ER -