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Microsatellite alternation in laryngeal squamous cell carcinomas / 临床耳鼻咽喉头颈外科杂志
Journal of Clinical Otorhinolaryngology Head and Neck Surgery ; (24): 241-244, 2009.
Artigo em Chinês | WPRIM | ID: wpr-748253
ABSTRACT
OBJECTIVE@#To examine the microsatellite instability and loss of heterozygosity in the pathogenic mechanism of laryngeal squamous cell carcinomas.@*METHOD@#Forty cases squamous cell carcinomas of larynx were analyzed by comparing tumorous tissues and normal tissues around with 3 microsatellite markers from chromosome 3, 5 and 11, using PCR and PGE-AgNO3 staining.@*RESULT@#Among the 40 cases of laryngeal squamous cell carcinomas, 87.5% (35/40) of samples showed microsatellite instability or loss of heterozygosity in one to three microsatellite markers. High frequent microsatellite abnormal occurred at D5S592, it was 70% (28/40). Then the mutation rate of D3s1228 was 52.5% (21/40).@*CONCLUSION@#Our study revealed that tumor suppressor genes nearby chromosome 3p14 and 5q23 regions related to the pathogenesis of squamous cell carcinomas of larynx. A correlation between microsatellite alternation and stage of the tumor were found in D3s1228 and D5s592 chromosome regions.
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Patologia / Carcinoma de Células Escamosas / Neoplasias Laríngeas / Genes Supressores de Tumor / Perda de Heterozigosidade / Instabilidade de Microssatélites / Genética / Estadiamento de Neoplasias Limite: Humanos Idioma: Chinês Revista: Journal of Clinical Otorhinolaryngology Head and Neck Surgery Ano de publicação: 2009 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Patologia / Carcinoma de Células Escamosas / Neoplasias Laríngeas / Genes Supressores de Tumor / Perda de Heterozigosidade / Instabilidade de Microssatélites / Genética / Estadiamento de Neoplasias Limite: Humanos Idioma: Chinês Revista: Journal of Clinical Otorhinolaryngology Head and Neck Surgery Ano de publicação: 2009 Tipo de documento: Artigo