Using comparative genomic hybridization (CGH), we have identified and mapped regions of DNA amplification in primary and metastatic osteosarcoma. Samples were obtained from four patients and ten independent xenogmfts. Sixty-four percent of the tumors showed increased DNA-sequence copy numbers, affec
Characterization of the 17p amplicon in human sarcomas: Microsatellite marker analysis
β Scribed by Maija Wolf; Maija Tarkkanen; Theo Hulsebos; Marcelo L. Larramendy; Anne Forus; Ola Myklebost; Lauri A. Aaltonen; Inkeri Elomaa; Sakari Knuutila
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- French
- Weight
- 171 KB
- Volume
- 82
- Category
- Article
- ISSN
- 0020-7136
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β¦ Synopsis
The structure of the 17p amplicon from 9 human sarcoma specimens evaluated by comparative genomic hybridization (CGH) has been studied by analyzing 28 microsatellite markers by PCR. Eleven sarcoma specimens showing no DNA copy number increases at 17p by CGH were analyzed as control samples. Five specimens were analyzed by Southern blotting using probes that have previously shown amplification at the 17p12 region in astrocytoma and high-grade osteosarcoma samples. Microsatellite marker analyses revealed that all samples but 1 showing copy number increases at 17p by CGH displayed allelic imbalance that confirmed the CGH findings. Seven of these 9 cases displayed gain in copy number by microsatellite marker analysis. Four cases displaying gain in copy number were associated with loss of heterozygosity at other loci. Southern blot analysis showed amplification in 3 cases, all of them had shown copy number increases by CGH and microsatellite marker analysis, except one case, which was not included in the microsatellite marker analysis. Our results reveal the complexity of the 17p amplicon in sarcomas, suggesting that multiple target genes are involved in tumorigenesis.
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