Analysis of the prostate cancer-susceptibility locus HPC20 in 172 families affected by prostate cancer

被引:35
作者
Bock, CH
Cunningham, JM
McDonnell, SK
Schaid, DJ
Peterson, BJ
Pavlic, RJ
Schroeder, JJ
Klein, J
French, AJ
Marks, A
Thibodeau, SN
Lange, EM
Cooney, KA
机构
[1] Univ Michigan, Sch Med, Dept Internal Med, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Dept Surg, Ann Arbor, MI 48109 USA
[3] Ann Arbor Dept Vet Affairs Med Ctr, Ann Arbor, MI USA
[4] Mayo Clin & Mayo Fdn, Dept Lab Med & Pathol, Rochester, MN 55905 USA
[5] Mayo Clin & Mayo Fdn, Dept Hlth Sci Res, Rochester, MN 55905 USA
[6] Univ Michigan, Sch Publ Hlth, Dept Epidemiol, Ann Arbor, MI 48109 USA
[7] Univ Michigan, Sch Publ Hlth, Dept Biostat, Ann Arbor, MI 48109 USA
关键词
D O I
10.1086/318797
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A recent study of hereditary prostate cancer has provided evidence for a prostate cancer-susceptibility locus, HPC20, which maps to 20q13. To assess further the potential contribution of this locus to prostate cancer susceptibility, we studied 172 unrelated families affected by prostate cancer, using 17 polymorphic markers across a 98.5-cM segment of chromosome 20 that contains the candidate region. Parametric analysis, allowing for heterogeneity, resulted in an overall HLOD score of 0.09 (P = .39) at D20S171, under the assumption of linkage in 6% of families. Mode-of-inheritance-free analysis of the entire data set resulted in a maximal Z(lr) score of 0.76 (LOD 0.13; P = .22) at the same location. The strongest evidence for linkage was seen in the subset of 16 black families (LOD 0.86; Z(lr) = 1.99; P = .23) between markers D20S893 and D20S120, near the putative location of HPC20. Although some positive results were observed, our linkage study does not provide statistically significant support for the existence of a prostate cancer-susceptibility locus HPC20 at 20q13.
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收藏
页码:795 / 801
页数:7
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