Using a polymerase chain reaction/microsatellite marker system, we demonstrated that 6 of 22 (27%) clinical stage B (early) primary prostate tumors showed loss of heterozygosity at one or more of five loci on chromosome 17. The sensitivity of this study was increased by use of a Phosphorlmager and s
Loss of chromosome arm 8p loci in prostate cancer: Mapping by quantitative allelic imbalance
β Scribed by Donal MacGrogan; Alina Levy; David Bostwick; Michael Wagner; Dan Wells; Robert Bookstein
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 791 KB
- Volume
- 10
- Category
- Article
- ISSN
- 1045-2257
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β¦ Synopsis
Abstract
A previous study of 18 primary or metastatic prostate cancers showed loss of genetic markers on chromosome 8; 10, or 16 in more than 50% of cases [Bergerheim USR et al. (1991) Genes Chromosom Cancer 3:215β220]. The small size and infiltrative nature of primary prostatic tumors have hindered efforts to assess allelic losses by traditional restriction fragment length polymorphism (RFLP)/Southern blotting methods. To improve the sensitivity and specificity of this analysis in early prostate cancer, we have amplified polymorphic microsatellite repeats by polymerase chain reaction (PCR), and have quantitated allelic imbalances with phosphor imaging technology. In this study, 63 primary prostate tumors and matched benign tissues obtained by radical prostatectomy were examined at 28 genetic loci on chromosome 8, all but five of which were located on the short arm. Twentyβnine (46%) of the 63 cases showed loss of at least one locus. Multiple adjacent loci, usually including the LPL and MSR genes in 8p22, were lost in 28 cases. In 10 of these, losses were observed at all informative loci on the p arm. In another 15 tumors, losses were restricted to subregions of the p arm by loci retained either distally toward the p terminus or proximally at the 8p 12β8p21 border, or both. In three tumors, two discrete regions of loss were observed within 8p, separated by several retained loci. Allelic loss of 8p loci was associated with higher tumor grade. These data are complementary to previous reports of allelic deletions in colorectal, hepatocellular, and nonβsmall cell lung cancers and suggest the existence of one or more pleotropic tumor suppressor genes on 8p. Genes Chromosom Cancer 10:151β159 (1994). Β© 1994 WileyβLiss, Inc.
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