Suppr超能文献

杂合性缺失研究表明,染色体1p臂含有肾嗜酸细胞瘤的一个肿瘤抑制基因。

Loss of heterozygosity studies indicate that chromosome arm 1p harbors a tumor supressor gene for renal oncocytomas.

作者信息

Thrash-Bingham C A, Salazar H, Greenberg R E, Tartof K D

机构信息

Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, PA, USA.

出版信息

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.

Abstract

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.

摘要

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。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验