Kimmelman A C, Ross D A, Liang B C
Clinical Pharmacology Branch, National Cancer Institute, Bethesda, Maryland, 20892, USA.
Genomics. 1996 Jun 1;34(2):250-4. doi: 10.1006/geno.1996.0277.
Molecular loss of heterozygosity studies on human gliomas have shown several regions on chromosome 10 frequently deleted in higher grade tumors, suggesting that chromosome 10 may contain several tumor suppressor genes. We assessed loss of heterozygosity with microsatellite markers in 20 gliomas, consisting of various grades and containing two chromosome 10 copies. The locus that exhibited the most loss (69%) was the region bordered by D10S249 and D10S558 and inclusive of D10S594, with a linkage distance of 3 cM. This region was noted to be deleted in various grades of tumor, including low- and high-grade tumors. These results suggest that chromosome region 10p15 is involved in human gliomas of diverse grades and that this region may harbor genes important in the development of and progression to the malignant phenotype.
对人类胶质瘤进行的杂合性分子缺失研究表明,10号染色体上的几个区域在高级别肿瘤中经常缺失,这表明10号染色体可能包含多个肿瘤抑制基因。我们使用微卫星标记评估了20例胶质瘤中的杂合性缺失情况,这些胶质瘤包括不同级别且含有两个10号染色体拷贝。缺失最多(69%)的位点是由D10S249和D10S558界定并包含D10S594的区域,连锁距离为3厘摩。该区域在包括低级别和高级别肿瘤在内的不同级别的肿瘤中均被发现有缺失。这些结果表明,染色体区域10p15参与了不同级别的人类胶质瘤,并且该区域可能含有在恶性表型的发生和发展中起重要作用的基因。