Evidence for a prostate cancer linkage to chromosome 20 in 159 hereditary prostate cancer families

被引:0
|
作者
Siqun L. Zheng
Jianfeng Xu
Sarah D. Isaacs
Kathy Wiley
Bao-li Chang
Eugene R. Bleecker
Patrick C. Walsh
Jeffrey M. Trent
Deborah A. Meyers
William B. Isaacs
机构
[1] University of Maryland School of Medicine,
[2] Baltimore,undefined
[3] MD,undefined
[4] USA,undefined
[5] Center for Human Genomics,undefined
[6] Wake Forest University School of Medicine,undefined
[7] Winston-Salem,undefined
[8] N.C.,undefined
[9] USA,undefined
[10] National Human Genome Research Institute,undefined
[11] National Institute of Health,undefined
[12] Bethesda,undefined
[13] MD,undefined
[14] USA,undefined
[15] Department of Urology,undefined
[16] Johns Hopkins Medical Institutions,undefined
[17] Baltimore,undefined
[18] MD,undefined
[19] USA,undefined
[20] Present address: Marburg 115,undefined
[21] Johns Hopkins Hospital,undefined
[22] 600 N. Wolfe Street,undefined
[23] Baltimore,undefined
[24] MD 21287,undefined
[25] USA,undefined
来源
Human Genetics | 2001年 / 108卷
关键词
Prostate Cancer; Susceptibility Locus; Recessive Model; Common Malignancy; Cancer Family;
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学科分类号
摘要
Prostate cancer is the most common malignancy diagnosed in men in the US. Genetic susceptibility to prostate cancer has been well documented. A region at chromosome 20q13 (HPC20) has been reported to be linked to a prostate cancer susceptibility gene. To confirm this finding, we genotyped 16 markers spanning ~95 cM on chromosome 20 in 159 hereditary prostate cancer (HPC) families. Positive (but not statistically significant) linkage scores were observed from 20pter to 20q11, with the highest non-parametric linkage (NPL) score for the complete dataset of 1.02 (P=0.15) being observed at D20S195 at 20q11. Evidence for linkage from parametric analyses with a dominant or a recessive model was weak. Interestingly, consistent with the original findings of linkage to 20 g higher linkage scores were observed in the subsets of families with a later age at diagnosis (≥65 years; n=80, NPL=1.94, P=0.029 at D20S186), fewer than five affected family members (n=69, NPL=1.74, P=0.037 at D20S889), or without male-to-male disease transmission (n=60, NPL=1.01, P=0.15 at D20S117). The region with positive linkage scores spanned ~60 cM from 20pter to 20q11 in these subsets of families. Our results are consistent with a prostate cancer susceptibility locus on chromosome 20.
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页码:430 / 435
页数:5
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