Large-scale association study identifies ICAM gene region as breast and prostate cancer susceptibility locus

被引:81
作者
Kammerer, S
Roth, RB
Reneland, R
Marnellos, G
Hoyal, CR
Markward, NJ
Ebner, F
Kiechle, M
Schwarz-Boeger, U
Griffiths, LR
Ulbrich, C
Chrobok, K
Forster, G
Praetorius, GM
Meyer, P
Rehbock, J
Cantor, CR
Nelson, MR
Braun, A
机构
[1] Sequenom Inc, San Diego, CA 92121 USA
[2] Univ Munich, Klinikum Innenstadt, Frauenklin 1, Munich, Germany
[3] Tech Univ Munich, Dept Obstet & Gynecol, D-8000 Munich, Germany
[4] Griffith Univ, Sch Hlth Sci, Genom Res Ctr, Gold Coast, Qld, Australia
[5] Urol Clin Munich Planegg, Munich, Germany
[6] Univ Tubingen Hosp, Inst Human Genet, Tubingen, Germany
[7] Genefinder Technol Ltd, Munich, Germany
关键词
D O I
10.1158/0008-5472.CAN-04-1788
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We conducted a large-scale association study to identify genes that influence nonfamilial breast cancer risk using a collection of German cases and matched controls and >25,000 single nucleotide polymorphisms located within 16,000 genes. One of the candidate loci identified was located on chromosome 19p13.2 [odds ratio (OR) = 1.5, P = 0.001]. The effect was substantially stronger in the subset of cases with reported family history of breast cancer (OR = 3.4, P = 0.001). The finding was subsequently replicated in two independent collections (combined OR = 1.4, P < 0.001) and was also associated with predisposition to prostate cancer in an independent sample set of prostate cancer cases and matched controls (OR = 1.4, P = 0.002). High-density single nucleotide polymorphism mapping showed that the extent of association spans 20 kb and includes the intercellular adhesion molecule genes ICAM1, ICAM4, and ICAM5. Although genetic variants in ICAM5 showed the strongest association with disease status, ICAM1 is expressed at highest levels in normal and tumor breast tissue. A variant in ICAM5 was also associated with disease progression and prognosis. Because ICAMs are suitable targets for antibodies and small molecules, these findings may not only provide diagnostic and prognostic markers but also new therapeutic opportunities in breast and prostate cancer.
引用
收藏
页码:8906 / 8910
页数:5
相关论文
共 42 条
[31]  
RISCH N, 1996, SCIENCE, V273, P15166
[32]   Searching for genetic determinants in the new millennium [J].
Risch, NJ .
NATURE, 2000, 405 (6788) :847-856
[33]   Score tests for association between traits and haplotypes when linkage phase is ambiguous [J].
Schaid, DJ ;
Rowland, CM ;
Tines, DE ;
Jacobson, RM ;
Poland, GA .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (02) :425-434
[34]   AP-1 as a regulator of cell life and death [J].
Shaulian, E ;
Karin, M .
NATURE CELL BIOLOGY, 2002, 4 (05) :E131-E136
[35]  
Sing CF, 1996, CIBA F SYMP, V197, P211
[36]  
SING CF, 1996, CIBA FOUND S, V197, P29
[37]   A comparison of Bayesian methods for haplotype reconstruction from population genotype data [J].
Stephens, M ;
Donnelly, P .
AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) :1162-1169
[38]   Intercellular adhesion molecule-5 induces dendritic outgrowth by homophilic adhesion [J].
Tian, L ;
Nyman, H ;
Kilgannon, P ;
Yoshihara, Y ;
Mori, K ;
Andersson, LC ;
Kaukinen, S ;
Rauvala, H ;
Gallatin, WM ;
Gahmberg, CG .
JOURNAL OF CELL BIOLOGY, 2000, 150 (01) :243-252
[39]   Establishment of genetic associations for complex diseases is independent of early study findings [J].
Trikalinos, TA ;
Ntzani, EE ;
Contopoulos-Ioannidis, DG ;
Ioannidis, JPA .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2004, 12 (09) :762-769
[40]   Insights into the functions of BRCA1 and BRCA2 [J].
Welcsh, PL ;
Owens, KN ;
King, MC .
TRENDS IN GENETICS, 2000, 16 (02) :69-74