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喉癌组织RB基因突变及其与临床分期的关系 被引量:2

Study of RB gene in carcinoma of larynx
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摘要 目的 :探讨喉癌组织中RB基因突变及其与临床分期的关系。方法 :用聚合酶链式反应和单链构象多态性 (PCR SSCP)对 90例喉癌标本进行检测。结果 :90例中 ,2例发生纯合性缺失 ,12例SSCP异常电泳 ,总突变率 15 .5 % (14 / 90 ) ;Ⅰ~Ⅱ期喉癌RB基因突变 5例 (13.9% ) ,Ⅲ~Ⅳ期RB基因突变 9例 (16 .7% ) ,两者之间差异无显著性意义。结论 :RB基因突变在喉癌的发生发展中起着一定的作用 ; Objective:To probe the mutations of RB gene in laryngeal carcinoma, and the relation between it and the clinical phase. Method: The mutations were detected by PCR SSCP (polymerase chain reaction single strand conformation polymorphism). Result:In laryngeal carcinoma, the mutations were identified in 14( 15.5 %) of 90 samples, of which 2 were large deletion, 12 were abnormal in electrophoresis of SSCP. The mutations of Ⅰ~Ⅱ stage tumor were 5( 13.9 %), of Ⅲ~Ⅳ were 9( 16.7 %), there wasn't a significant difference between them. Conclusion:RB gene mutation takes part in the development of laryngeal carcinoma. But there wasn't relation between RB gene mutation and the course of laryngeal carcinoma.
出处 《临床耳鼻咽喉科杂志》 CSCD 北大核心 2003年第2期89-91,共3页 Journal of Clinical Otorhinolaryngology
关键词 喉肿瘤 聚合酶链反应 RB基因 Laryngeal neoplasms Polymerase chain reaction RB gene
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  • 1[1]Stahl A, Levy N, Wadzynska T, et al. The genetics of retinoblstoma. Ann Genet, 1994,37:172-178.
  • 2[2]Gowell J K. Genetics and cytogentics of retinoblstoma. Cancer Genet Cytogenet, 1992,64:1-11.
  • 3[3]Shimizu T, Toguchida J, Kato M V, et al. Detection of mutation of the RB1 gene in retinoblstoma patients by using exon-by-exon PCR-SSCP analysis. Am J Hum Genet, 1994,54:793-800.
  • 4[4]Blanquet V, Turleau C, Gross-Morand M S, et al. Spectrum of germline mutation in the RB1 gene: A study of 232 patients with hereditary and non hereditary retinoblstoma. Hum Mol Genet, 1995,4:383-388.
  • 5[5]Lohman D R, Brand B, Hopping W, et al. The Spectrum of RB1 germ-line mutation in hereditary retinoblstoma. Am J Hum Genet, 1996,58:940-949.

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