Frequent Loss of Chromosome Arms 8p and 13q in Collecting Duct Carcinoma (CDC) of the Kidney

✍ Scribed by Mark Schoenberg; James D. Brooks; Fray F. Marshall; Jonathan I. Epstein; William B. Isaacs; Paul Cairns; David Sidransky

• Book ID: 102846806
• Publisher: John Wiley and Sons
• Year: 1995
• Tongue: English
• Weight: 520 KB
• Volume: 12
• Category: Article
• ISSN: 1045-2257
• DOI: 10.1002/gcc.2870120115

✦ Synopsis

Collecting duct carcinoma (CDC) is a malignant renal neoplasm that is believed t o arise from the epithelium of the ducts of Bellini in the distal nephron. These tumors are clinically aggressive and more often occur in a younger population than is typical of the more common clear cell renal carcinoma (RCC). Using highly informative polymorphic microsatellite markers on chromosome arms 3p, Sq, 6q, 8p, 9p, 9q, I I p, I 3q, I7p, and I8q, we analyzed DNA from nonmalignant and tumor tissue in 6 cases of CDC. We found no evidence of 3p loss of heterozygosity (LOH) in these renal tumors by using multiple markers, a finding that distinguishes CDC from RCC in which 3p LOH has frequently been observed. We found LOH of 8p in 50% of the tumors examined; in addition, we observed LOH of 13q in 50% of the tumors studied. Interestingly, 8p LOH may be associated with high stage and poor clinical prognosis. These data suggest that the molecular events responsible for the development of CDC differ from those associated with the origin of RCC, and that tumor suppressor genes on 8p and 13q may be involved in the pathogenesis of CDC. Genes Chromosam Cancer 12:76-80 (1995).