FREQUENT ALLELIC IMBALANCE AND CYTOGENETIC DELETION ON THE SHORT ARM OF CHROMOSOME 1 IN NASOPHARYNGEAL CARCINOMA
Objective: To construct a fine map of the loss of chromosome lpter-p36.11 region in nasopharyngeal carcinoma (NPC) using PCR-LOH technique. Methods:DNA extracted from separated cancerous cells and their mated noncancerous lymphocytes from 47 cases of NPC biopsies were analyzed by means of PCR-LOH to...
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Published in | Chinese journal of cancer research Vol. 16; no. 1; pp. 5 - 10 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
Department of Nuclear Medicine,the Second Municipal Hospital of Shenzhen,Shenzhen 518035%Research Department,Cancer Center,Sun Yat-sen University,Guangzhou 510060
01.03.2004
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Subjects | |
Online Access | Get full text |
ISSN | 1000-9604 1993-0631 |
DOI | 10.1007/BF02974858 |
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Summary: | Objective: To construct a fine map of the loss of chromosome lpter-p36.11 region in nasopharyngeal carcinoma (NPC) using PCR-LOH technique. Methods:DNA extracted from separated cancerous cells and their mated noncancerous lymphocytes from 47 cases of NPC biopsies were analyzed by means of PCR-LOH to detect 20 loci spanning chromosome lpter-p36.11 region in NPC.Results: In 47 NPC cases, 37 (82.2%) cases showed at least one loci LOH. The highest frequency of less of heterozygosity (LOH) at all 20 loci was found at loci DIS234 (50. 0%) on lp36.13 and loci DIS2644 (37.5%) on lp36.22. There was a statistically significant difference between DIS234 LOH frequency (60%, 9/15) in early stage and that (50.0%, 8/16) in advanced stage (P>0.05). Of all 20 STSs (sequence tqgged-site, STS), DIS243 (37.5%) and DIS199 (30.2%) showed the highest frequency of MI(microsatellite instability) on lp36.33 and lp36.21, respectively. In addition,several cases showed a contiguous stretch of allelic loss in a different level. Conclusion: Two minimal deletion regions (MDR) on the short arm of chromosome 1 were seated at lp36.13(DIS234, 2.0cm) and lp36.22 (DIS436-DIS2644, 6.3cm) respectively, indicating that one or more candidate tumor suppressor gene (TSG) in the two regions may be involved in NPC pathogenesis in an early clinical stage. |
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Bibliography: | 11-2591/R R739.63 |
ISSN: | 1000-9604 1993-0631 |
DOI: | 10.1007/BF02974858 |