LOSS OF CHROMOSOME-17 LOCI IN PROSTATE-CANCER DETECTED BY POLYMERASE CHAIN-REACTION QUANTITATION OF ALLELIC MARKERS

被引:21
作者
BROTHMAN, AR
STEELE, MR
WILLIAMS, BJ
JONES, E
ODELBERG, S
ALBERTSEN, HM
JORDE, LB
ROHR, LR
STEPHENSON, RA
机构
[1] UNIV UTAH,SCH MED,DEPT HUMAN GENET,SALT LAKE CITY,UT 84132
[2] UNIV UTAH,SCH MED,DEPT PEDIAT,SALT LAKE CITY,UT 84132
[3] UNIV UTAH,SCH MED,DEPT PATHOL,SALT LAKE CITY,UT 84132
[4] UNIV UTAH,SCH MED,DEPT UROL,SALT LAKE CITY,UT 84132
关键词
D O I
10.1002/gcc.2870130408
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Using a polymerase chain reaction/microsatellite marker system, we demonstrated that 6 of 22 (27%) clinical stage B (early) primary prostate tumors showed loss of heterozygosity at one or more of five loci on chromosome 17. The sensitivity of this study was increased by use of a Phosphorlmager and statistical analysis of replicate tumor-normal DNA pairs. Two patients showed tumor-specific interstitial loss at a locus in close proximity to the familial breast cancer gene BRCA1. These findings suggest that genes on the proximal long arm of chromosome 17 play a pivotal role in the early development of at least a subset of prostatic tumors. (C) 1995 Wiley-Liss, Inc.
引用
收藏
页码:278 / 284
页数:7
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