Loss of Heterozygosity of Chromosome 17p in Brain Tumors
Journal of Korean Neurosurgical Society
;
: 23-29, 1992.
Artículo
en Coreano
| WPRIM
| ID: wpr-127937
ABSTRACT
With the methods of restriction fragment length polymorphisms(RFLPs) and southern blot analysis, gene deletion of chromosome 17p in 16 cases of brain tumors, was investigated. There were 4 cases of glioblastoma multiforme, 1 case of anaplastic astrocytoma, 4 cases of low grade astrocytoma, 3 cases of oligodendroglioma, and 4 cases of meningioma. Among restriction fragment length polymorphism(RFLP) DNA located in chromosome 17p, p144D 6 and p SNZ 22 were imployed as the probes. In eight of 16 cases(50%) constitutional heterozygosity was observe dfor p144 D6 probe on the short arm of chromosome 17, and in nine of 16 cases(56%) for PYNZ 22.1 probe. With both probes constitutional heterozygosity was observed in thirteen of 16 cases(81%). And the loss of constitutional heterozygosity was detected in two of 14 informative cases. Although, with the malignant gliomas, including 4 cases of glioblastoma multiforme and 1 case of anaplastic astrocytoma, two of 4 informative cases showed loss of constitutional heterozygosty, None of 9 informative cases showed loss of heterozygosity with the other brain tumors(low grade astrocytoma, oligodendroglioma, and meningioma).
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Oligodendroglioma
/
Brazo
/
Astrocitoma
/
Cromosomas Humanos Par 17
/
Polimorfismo de Longitud del Fragmento de Restricción
/
Encéfalo
/
Neoplasias Encefálicas
/
ADN
/
Southern Blotting
/
Eliminación de Gen
Idioma:
Coreano
Revista:
Journal of Korean Neurosurgical Society
Año:
1992
Tipo del documento:
Artículo
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