Genome-wide linkage of 77 families from the African American Hereditary Prostate Cancer Study (AAHPC)

被引:17
|
作者
Baffoe-Bonnie, Agnes B.
Kittles, Rick A.
Gillanders, Elizabeth
Ou, Liang
George, Asha
Robbins, Christiane
Ahaghotu, Chiledum
Bennett, James
Boykin, William
Hoke, Gerald
Mason, Terry
Pettaway, Curtis
Vijayakumar, Srinivasan
Weinrich, Sally
Jones, Mary P.
Gildea, Derek
Riedesel, Erica
Albertus, Julie
Moses, Tracy
Lockwood, Erica
Klaric, Meghan
Faruque, Mezbah
Royal, Charmaine
Trent, Jeffrey M.
Berg, Kate
Collins, Francis S.
Furbert-Harris, Paulette M.
Bailey-Wilson, Joan E.
Dunston, Georgia M.
Powell, Isaac
Carpten, John D.
机构
[1] TGen, Genet Basis Human Dis Div, Phoenix, AZ 85004 USA
[2] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
[3] NHGRI, NIH, Bethesda, MD 20892 USA
[4] Ohio State Univ, Ctr Comprehens Canc, Columbus, OH 43210 USA
[5] Howard Univ, Natl Human Genome Ctr, Washington, DC USA
[6] Howard Univ, Div Urol, Washington, DC USA
[7] Midtown Urol, Atlanta, GA USA
[8] Columbia Presbyterian Med Ctr, New York, NY 10032 USA
[9] Michael Reese Hosp, Chicago, IL USA
[10] Univ Texas, MD Anderson Canc Ctr, Houston, TX 77030 USA
[11] Univ Illinois, Chicago, IL USA
[12] Univ S Carolina, Columbia, SC 29208 USA
[13] Howard Univ, Dept Microbiol, Washington, DC 20059 USA
[14] Wayne State Univ, Karmanos Canc Inst, Detroit, MI USA
来源
PROSTATE | 2007年 / 67卷 / 01期
关键词
genetic susceptibility; aggressive disease; HPC2/ELAC2; metastases; genetic burden; 1-LOD support interval;
D O I
10.1002/pros.20456
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND. The African American Hereditary Prostate Cancer (AAHPC) Study was designed to recruit families with early-onset disease fulfilling criteria of >= 4 affected. METHODS. We present a similar to 10 cM genome-wide linkage (GWL) analysis on 77 families including 254 affected and 274 unaffected genotyped. RESULTS. Linkage analysis revealed three chromosomal regions with GENEHUNTER multipoint HLOD scores >= 1.3 for all 77 families at 11q22,17p11, and Xq21. One family yielded genome-wide significant evidence of linkage (LOD = 3.5) to the 17p11 region with seven other families >= 23 in this region. Twenty-nine families with no-male-to-male (MM) transmission gave a peak HLOD of 1.62 (alpha = 0.33) at the Xq21 locus. Two novel peaks >= 0.91 for the 16 families with '> 6 affected' occurred at 2p21 and 22q12. CONCLUSIONS. These chromosomal regions in the genome warrant further follow-up based on the hypothesis of multiple susceptibility genes with modest effects, or several major genes segregating in small subsets of families.
引用
收藏
页码:22 / 31
页数:10
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