Detection of chromosome 8 anomalies in ovarian carcinoma by fluorescence in situ hybridization / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
;
(6): 59-60, 2003.
Artigo
em Chinês
| WPRIM
| ID: wpr-248499
ABSTRACT
<p><b>OBJECTIVE</b>To detect the relationship between chromosomal anomalies and the pathogenesis, development and prognosis of ovarian carcinoma.</p><p><b>METHODS</b>Thirty-six specimens of ovarian carcinoma (n=12), ovarian benign tumor (n=12), and normal ovary (n=12) were examined by fluorescence in situ hybridization (FISH).</p><p><b>RESULTS</b>Twelve cases of mutations, including trisomy 8, monosomy 8 or tetraploid 8 chromosomal anomalies, were found in the group of ovarian carcinoma, making up 100% (12/12). Three cases of trisomy 8 chromosomal anomalies were found in the group of ovarian benign tumor, accounting for 25% (3/12). No anomaly was found in the normal group. There were significant differences between the three groups, P<0.001.</p><p><b>CONCLUSION</b>The above anomalies of chromosome 8 are significantly associated with the pathogenesis and development of ovarian carcinoma. The anomalies may occur in the early stage of the carcinoma, and may be significantly associated with the pathological differentiation and clinical stage of the case.</p>
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Neoplasias Ovarianas
/
Trissomia
/
Cromossomos Humanos Par 8
/
Aberrações Cromossômicas
/
Hibridização in Situ Fluorescente
/
Genética
/
Aneuploidia
/
Métodos
/
Monossomia
Tipo de estudo:
Estudo diagnóstico
Limite:
Adolescente
/
Adulto
/
Idoso
/
Feminino
/
Humanos
Idioma:
Chinês
Revista:
Chinese Journal of Medical Genetics
Ano de publicação:
2003
Tipo de documento:
Artigo
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