Histologic-Genetic Mapping by Allele-Specific PCR Reveals Intraurothelial Spread of p53 Mutant Tumor Clones

• Published in: Laboratory investigation Vol. 82; no. 11; pp. 1553 - 1561
• Main Authors: Stoehr, Robert, Knuechel, Ruth, Boecker, Joerg, Blaszyk, Hagen, Schmitt, Ruediger, Filbeck, Thomas, Hofstaedter, Ferdinand, Hartmann, Arndt
• Format: Journal Article
• Language: English
• Published: New York, NY Elsevier Inc 01.11.2002; Nature Publishing; Nature Publishing Group
• Subjects: Aged; Alleles; Biological and medical sciences; Female; Genes, p53; Humans; Immunohistochemistry; Loss of Heterozygosity; Male; Medical sciences; Middle Aged; Mutation; Nephrology. Urinary tract diseases; Polymerase Chain Reaction - methods; Tumor Suppressor Protein p53 - analysis; Tumors of the urinary system; Urinary Bladder Neoplasms - genetics; Urinary Bladder Neoplasms - pathology; Urinary tract. Prostate gland; Human; Immunohistochemistry; Urinary system disease; Malignant tumor; Urinary tract disease; Transitional cell carcinoma; Polymerase chain reaction; Pathology; Allele; TP53 Gene; Urinary bladder; Dissemination; Tumor progression; Cytogenetics; Bladder disease; Mutation; Molecular biology; Clone; Tumor suppressor gene
• ISSN: 0023-6837; 1530-0307
• DOI: 10.1097/01.LAB.0000035022.29742.85

Common and clinically important features of urothelial carcinomas are multifocality and a high rate of recurrence. Molecular studies demonstrated that multifocal tumors are frequently composed of one tumor clone spreading throughout the urothelial tract. A combination of histologic and genetic mapping of cystectomy specimens from bladder cancer patients is a valuable tool to study bladder carcinogenesis and tumor cell spread by correlating urothelial morphologic features and defined genetic alterations. In the present study, the primary tumors of 14 cystectomy specimens were investigated for p53 protein overexpression by immunohistochemistry and p53 gene mutation by genomic sequencing. Seven tumors showed a strong nuclear staining for the p53 protein. In six of seven tumors, a p53 gene mutation was detected. Allele-specific PCR of defined p53 mutations was established in five of six cases with a p53 mutation. Subsequent screening of the entire urothelial lining of each cystectomy specimen by allele-specific PCR revealed p53-mutant cell clones in urothelial patches with carcinoma in situ and dysplasia, but also frequently in histomorphologically normal urothelium adjacent to the tumor. The pattern of tumor cell spread indicated a continuous intraurothelial growth of the p53-mutant clone. P53 immunohistochemistry visually confirmed the presence of mutant cells in most of these samples. We conclude that allele-specific PCR is a highly sensitive and reliable method for tracking specific p53 mutant clones in the urothelium. Moreover, the detection of p53-mutant cells in histologically normal or preneoplastic urothelial areas in four patients with invasive bladder cancer indicates an extensive intraurothelial tumor cell spread. The excellent correlation of immunohistochemically positive urothelial patches with the presence of a specific mutation highlights the biologic significance of p53-positive cells in the urothelium of tumor patients.