In order to demonstrate the relationship between microsatellite instability and other types of genomic instability, a series of 56 sporadic colorectal carcinomas was investigated by flow cytometrical ploidy analysis, oligonucleotide fingerprinting, and microsatellite polymerase chain reaction (PCR).
Genomic instability occurs in colorectal carcinomas but not in adenomas
β Scribed by Joanne Young; Barbara Leggett; Corinne Gustafson; Michael Ward; Jeffrey Searle; Lesley Thomas; Ron Buttenshaw; Georgia Chenevix-Trench
- Book ID
- 102260075
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 355 KB
- Volume
- 2
- Category
- Article
- ISSN
- 1059-7794
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β¦ Synopsis
Genomic instability, as demonstrated by the presence of additional alleles at short tandemly repeated (STR) loci, has recently been observed in colorectal tumours from individuals with hereditary nonpolyposis colorectal cancer (HNPCC), and in some sporadic tumours. These neoplasms have been called replication error positive (RER+). In this study, we confirm the presence of genomic instability in a proportion of unselected colorectal carcinomas but find no evidence of instability in adenomas. We further report replication errors in a tetranucleotide sequence, and in STRs within two tumour suppressor genes. 108 colorectal adenocarcinomas and 46 adenomas were analysed for the presence of variant bands at 4-15 microsatellite markers. Seven (6.5%) of carcinomas were RER+, four of which originated from the proximal colon. Analysis of the adenomas and of matched adenoma-carcinoma and carcinoma-metastatic samples from four patients suggests that the replication errors may occur during the development of carcinomas but are rare in adenomas.
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