Devlin J, Keen A J, Knowles M A
Molecular Genetics Laboratory, Marie Curie Research Institute, Oxted, Surrey.
Oncogene. 1994 Sep;9(9):2757-60.
We have screened 165 cases of primary transitional cell carcinoma of the bladder for loss of heterozygosity of markers on chromosome 9. High density deletion mapping was then carried out on a panel of 16 tumours with partial deletions of 9p using 15 microsatellite markers. Seven tumours had hemizygous deletions which included small interstitial losses and large terminal deletions. Homozygous deletions of one or more markers were identified in the remaining 9 tumours. By comparing the limits of hemi- and homozygous deletions in these tumours we have defined a single common region of 2cM flanked by IFNA and D9S171.
我们对165例原发性膀胱移行细胞癌进行了9号染色体上标记杂合性缺失的筛查。然后,使用15个微卫星标记,对一组16例9p部分缺失的肿瘤进行了高密度缺失图谱分析。7例肿瘤存在半合子缺失,包括小的间质缺失和大的末端缺失。在其余9例肿瘤中鉴定出一个或多个标记的纯合子缺失。通过比较这些肿瘤中半合子和纯合子缺失的范围,我们确定了一个2cM的单一共同区域,其两侧为IFNA和D9S171。