A systematic analysis of both tumors and the surrounding urothelium to help identify what lies behind the mechanism of multifocal tumor development has not yet been performed. In this study we investigated chromosome 1, 7, 9, and 17 aneusomy in 25 superficial papillary carcinomas and in 51 tissue samples taken from sites of macroscopically uninvolved urothelium surrounding the tumors, using the fluorescence in situ hybridization method. Our data demonstrated a close genetic relationship between all examined tumors normal-appearing mucosa. Numeric aberrations of chromosomes 1, 7, 9, and 17 were found to exhibit similar patterns in all analyzed specimens, although with different frequencies. Copyright 2003 Elsevier Inc. All rights reserved
Objective To determine if changes in chromosome 7 and 17 copy number can be used to predict recurren...
Bladder cancer is a common neoplasm worldwide, consisting mainly of transitional cell carcinomas, wh...
Aims: To evaluate a panel of well known genetic alterations for frequency of changes in bladder canc...
In order to understand the origin of bladder cancer, very early urothelial lesions must be investiga...
Multifocality and recurrence are clinically important features of urothelial carcinomas of the urina...
To define the genetic changes of flat urothelial lesions, carcinoma in situ (CIS) and moderate dyspl...
In the present study, different stages of transitional cell carcinoma of the bladder were analyzed b...
We evaluated the genetic changes in bladder cancer biopsy by fluorescence in situ hybridization (FIS...
Objective: To understand developmental characteristics of urinary bladder carcinomas (UBC) by evalua...
The processes of intraepithelial migration, intraluminal seeding, and field cancerization as models ...
Multifocality and recurrence of urothelial carcinoma may result from either the field effect of carc...
Bladder cancer is the second common malignant urological neoplasia. Most of the tumors are superfici...
Bladder carcinoma with transitional cells is the most frequent neoplasia in the urinary system, but ...
Urinary bladder carcinomas (UBC) frequently recur. During the intervals “free‐ofneoplasia”, between ...
A multiprobe interphase fluorescence in situ hybridization (I-FISH) approach has become a useful a...
Objective To determine if changes in chromosome 7 and 17 copy number can be used to predict recurren...
Bladder cancer is a common neoplasm worldwide, consisting mainly of transitional cell carcinomas, wh...
Aims: To evaluate a panel of well known genetic alterations for frequency of changes in bladder canc...
In order to understand the origin of bladder cancer, very early urothelial lesions must be investiga...
Multifocality and recurrence are clinically important features of urothelial carcinomas of the urina...
To define the genetic changes of flat urothelial lesions, carcinoma in situ (CIS) and moderate dyspl...
In the present study, different stages of transitional cell carcinoma of the bladder were analyzed b...
We evaluated the genetic changes in bladder cancer biopsy by fluorescence in situ hybridization (FIS...
Objective: To understand developmental characteristics of urinary bladder carcinomas (UBC) by evalua...
The processes of intraepithelial migration, intraluminal seeding, and field cancerization as models ...
Multifocality and recurrence of urothelial carcinoma may result from either the field effect of carc...
Bladder cancer is the second common malignant urological neoplasia. Most of the tumors are superfici...
Bladder carcinoma with transitional cells is the most frequent neoplasia in the urinary system, but ...
Urinary bladder carcinomas (UBC) frequently recur. During the intervals “free‐ofneoplasia”, between ...
A multiprobe interphase fluorescence in situ hybridization (I-FISH) approach has become a useful a...
Objective To determine if changes in chromosome 7 and 17 copy number can be used to predict recurren...
Bladder cancer is a common neoplasm worldwide, consisting mainly of transitional cell carcinomas, wh...
Aims: To evaluate a panel of well known genetic alterations for frequency of changes in bladder canc...