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Korean Journal of Obstetrics & Gynecology 2003;46(1):38-43.
Published online January 1, 2003.
Chromosomal gains and losses in primary ovarian carcinomas by comparative genomic hybridization.
Soo Hun Cho, Mee Hye Kim, Nak Woo Lee, Young Tae Kim, Kyu Wan Lee
1Department of Obstetrics and Gynecology, College of Medicine, Korea University, Korea.
2Sewha Pediatric Clinic, Seoul, Korea.
Abstract
OBJECTIVE
Comparative genomic hybridization was performed to evaluate DNA sequence copy number changes in human ovarian carcinomas from paraffin-embedded tissue blocks. PATIENTS AND METHODS: DNA from 20 cases of primary ovarian carcinomas underwent comparative genomic hybridization to evaluate the extent of genetic gains or losses in a test sample. RESULTS: In thirteen cases of 20 samples, varying degree of genetic imbalances was observed. Of the remaining 7 cases, two revealed normal, five failed to yield a result. Most common genetic imbalances are 8q22.2-q24 site amplification and 12p site amplification, where c-myc gene and k-ras gene respectively are included. Second most common site of genetic imbalance is 7p21-pter site deletion. CONCLUSION: Our results have shown many chromosomal alterations in human ovarian carcinomas, and these sites are known previously as oncogene or tumor-suppression gene, and some sites are not known specific cancer associated sites. Our data can be useful for screening chromosomal changes and molecular mechanism of human ovarian carcinogenesis.
Key Words: ovarian cancer, comparative genomic hybridization, FISH, chromosomal change
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