Thrash-Bingham C A, Salazar H, Greenberg R E, Tartof K D
Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, PA, USA.
Genes Chromosomes Cancer. 1996 May;16(1):64-7. doi: 10.1002/(SICI)1098-2264(199605)16:1<64::AID-GCC9>3.0.CO;2-1.
We carried out a complete genome scan for loss of heterozygosity (LOH) in four renal oncocytomas by using highly polymorphic CA repeat microsatellite loci. Three of the four tumors exhibited LOH for chromosome arm 1p, and the oncocytomas of both female patients lost Xq. Therefore, these chromosome arms may harbor tumor suppressor genes involved in the etiology of this disease. Although the genomes of ontocytomas are relatively stable, two different microsatellite loci in one tumor were mutated by + or - 2 nt. Similar alterations in CA repeats that are probably due to spontaneous mutation have been observed in renal cell carcinomas.
我们通过使用高度多态性的CA重复微卫星位点,对4例肾嗜酸细胞瘤进行了杂合性缺失(LOH)的全基因组扫描。4个肿瘤中有3个显示1号染色体短臂存在LOH,两名女性患者的嗜酸细胞瘤均丢失了X染色体长臂。因此,这些染色体臂可能含有与该疾病病因相关的肿瘤抑制基因。虽然嗜酸细胞瘤的基因组相对稳定,但一个肿瘤中的两个不同微卫星位点发生了+2或 -2个核苷酸的突变。在肾细胞癌中也观察到了可能由于自发突变导致的CA重复序列的类似改变。