Abstract |
The clinical course of astrocytoma grade 2 (A2) is highly variable and is not reflected by morphological characteristics. Earlier studies using small series of A2 cases suggest that in situ hybridization (ISH) with chromosome-specific DNA probes allows for frequent detection of aneusomy 1, trisomy 7, and monosomy 10. The role of trisomy 7 in astrocytoma carcinogenesis is disputed, however, because of its presence in non-neoplastic brain tissue, as detected by karyotyping. Our objective was to investigate whether there was a correlation between chromosomal aberrations and survival in a series of 47 cases of A2. All cases were evaluated for numerical aberrations of chromosomes 1, 7, and 10 by ISH. Chromosomal aberrations were detected in 68% of cases of A2. Trisomy/polysomy 7 was seen in 31 cases (66%), 22 of which (47%) had a high percentage of this numerical aberration. Only 11 of these 22 cases also showed aneusomy for 1 or 10. No cells or only a few cells with aberrations were detected in non-neoplastic control samples. Using Kaplan-Meier analysis, trisomy/polysomy 7 correlated significantly with shorter survival. Hence, as determined by ISH, trisomy/polysomy 7 is absent in non-neoplastic brain tissue and is frequently detected in A2, correlating with the malignant progression of the disease.
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Authors | Peter H Wessels, Albert Twijnstra, Alfons G H Kessels, Bela Krijne-Kubat, Paul H Theunissen, Monique I J Ummelen, Frans C S Ramaekers, Anton H Hopman |
Journal | Genes, chromosomes & cancer
(Genes Chromosomes Cancer)
Vol. 33
Issue 3
Pg. 279-84
(Mar 2002)
ISSN: 1045-2257 [Print] United States |
PMID | 11807985
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright 2002 Wiley-Liss, Inc. |
Topics |
- Adult
- Astrocytoma
(genetics, mortality, pathology)
- Brain Neoplasms
(genetics, mortality, pathology)
- Chromosome Aberrations
- Chromosomes, Human, Pair 7
(genetics)
- Gene Amplification
(genetics)
- Humans
- In Situ Hybridization
(methods)
- Prognosis
- Survival Rate
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