Rasheed B K, Fuller G N, Friedman A H, Bigner D D, Bigner S H
Department of Pathology, Duke University Medical Center, Durham, North Carolina 27710.
Genes Chromosomes Cancer. 1992 Jul;5(1):75-82. doi: 10.1002/gcc.2870050111.
Cytogenetic and RFLP studies have shown that chromosome 10 is frequently lost in tumor cells from glioblastomas, suggesting that a suppressor gene important in tumorigenesis is present on this chromosome. Forty-one tumors were examined for loss of heterozygosity at 23 loci on chromosome 10 to determine the smallest common deletion interval on this chromosome. Seven tumors did not lose heterozygosity for any of the markers. Twenty-three tumors lost an allele for all the informative loci. In 11 tumors heterozygosity was maintained at some loci and lost at other loci, indicating partial deletion of chromosome 10. The common region of deletion in these 11 tumors was located in 10q24-q26 between the markers pHUK-8 and pMCT122.2.
细胞遗传学和限制性片段长度多态性(RFLP)研究表明,在成胶质细胞瘤的肿瘤细胞中,10号染色体经常缺失,这表明该染色体上存在一个在肿瘤发生中起重要作用的抑癌基因。对41个肿瘤进行了检测,以确定10号染色体上23个位点的杂合性缺失情况,从而确定该染色体上最小的共同缺失区间。7个肿瘤在任何标记位点均未发生杂合性缺失。23个肿瘤在所有信息位点均丢失了一个等位基因。在11个肿瘤中,一些位点的杂合性得以保留,而另一些位点的杂合性则丢失,这表明10号染色体发生了部分缺失。这11个肿瘤的共同缺失区域位于标记pHUK - 8和pMCT122.2之间的10q24 - q26区域。