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肾母细胞瘤WT_1基因缺失
引用本文:张卫星,宋东奎,高永亮,步星耀,李中凌,杨锦健,王瑞.肾母细胞瘤WT_1基因缺失[J].现代肿瘤医学,2000(4).
作者姓名:张卫星  宋东奎  高永亮  步星耀  李中凌  杨锦健  王瑞
作者单位:河南医科大学第一附属医院泌尿外科!郑州45005(张卫星,宋东奎,步星耀,李中凌,杨锦健),荥阳市人民医院外科!荥阳450100(高永亮),河南医科大(王瑞)
摘    要:目的 对 30例散发性肾母细胞瘤WT1基因缺失进行检测 ,并分析其与组织类型的关系。方法 采用Southern印迹分子杂交技术。结果  2例WT1基因内缺失为间质优势型肾母细胞瘤。结论 肾母细胞瘤的病因学十分复杂 ,WT1基因缺失可能与间质优势型肾母细胞瘤的发生有关。

关 键 词:肾母细胞瘤  基因  Southern印迹分子杂交技术

Deletion of WT_1 in wilms tumor.
ZHANG Wei xing,SONG Dong kui,GAO Yong liang et al.Deletion of WT_1 in wilms tumor.[J].Journal of Modern Oncology,2000(4).
Authors:ZHANG Wei xing  SONG Dong kui  GAO Yong liang
Institution:ZHANG Wei xing,SONG Dong kui,GAO Yong liang et al. Department of Urology,the First Affiliated Hospital of Henan Medical University. Zhengzhou 450052,China
Abstract:Objective To study WT 1 gene from 30 cases of sporadic wilms tumor.Methods WT 1 gene was studied by Southern bolt hybridization with WT 1 cDNA probe.Results Two cases with intragenic deletions of WT 1 gene were histologically classified as stroma predominated wilms' tumor. Conclusion The etiology of wilms' tumor is complex, the deletion of WT 1 gene may be correlated with stroma predominated wilms tumor.
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