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机构地区:[1]华西医科大学肿瘤研究所
出 处:《中华医学遗传学杂志》1994年第2期75-77,共3页Chinese Journal of Medical Genetics
摘 要:首次应用生物素-14-dUTP标记Rb3.8kb探针,结合亲合素-碱性磷酸酶发光及自显影法,对Rb基因在鼻咽癌中存在状态进行了研究。杂交结果表明,3例正常胎儿鼻咽组织出现分子量为12.8、10.2、8.0、6.2、5.6、5.2及4.8kb的7条杂文区带,11例鼻咽癌组织均发现有Rb基因缺失或失活,其中4例为5.6kb片段缺失,4例为4.8kb缺失并有2例伴5.6kb减弱,2例为10.2kb缺失,1例为5.6及5.2kb片段显著减弱,说明在上述11例鼻咽癌中均有Rb基因的改变。这种高频率的异常变化,提示Rb基因的缺失或失活,与鼻咽癌的发生有密切关系。The status of Rb gene in nasopharyngeal carcinoma(NPC)and normal fetal nasopharynx tissues were studied by using biotin-14-dUTP labeled Rb cDNA 3.8kb probe in combination with streptavidin alkaline phosphatase luminescent detection system.Seven hybridizing bands of 12.8,10.2,8.0,6.2,5.6,5.2 and 4.8kb in DNA from 3 cases of normal fetal nasopharynx tissues as controls were observed.The structural abnormal alterations of Rb gene in DNA from 11 cases of NPC were studied,in which ob served were the deletion of 5. 6kb fragment in 4 cases,deletion of 4.8kb fragnient in 4 cases,deletion of 10.2kb fragment in 2 cases and the obvious loss of activity of both 5.6 and 5.2kb fragment in 1 case.The results implied that the alterations of the deletion or loss of activity of Rb gene with high frequency might be associated with the carcinogenesis of NPC.
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