Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus.

A locus at 19p13 is associated with breast cancer (BC) and ovarian cancer (OC) risk. Here we analyse 438 SNPs in this region in 46,451 BC and 15,438 OC cases, 15,252 BRCA1 mutation carriers and 73,444 controls and identify 13 candidate causal SNPs associated with serous OC (P=9.2 × 10(-20)), ER-negative BC (P=1.1 × 10(-13)), BRCA1-associated BC (P=7.7 × 10(-16)) and triple negative BC (P-diff=2 × 10(-5)). Genotype-gene expression associations are identified for candidate target genes ANKLE1 (P=2 × 10(-3)) and ABHD8 (P<2 × 10(-3)). Chromosome conformation capture identifies interactions betw... Mehr ...

Verfasser: Lawrenson, K
Kar, S
McCue, K
Kuchenbaeker, K
Michailidou, K
Tyrer, J
Beesley, J
Ramus, SJ
Li, Q
Delgado, MK
Lee, JM
Aittomäki, K
Andrulis, IL
Anton-Culver, H
Arndt, V
Arun, BK
Arver, B
Bandera, EV
Barile, M
Barkardottir, RB
Barrowdale, D
Beckmann, MW
Benitez, J
Berchuck, A
Bisogna, M
Bjorge, L
Blomqvist, C
Blot, W
Bogdanova, N
Bojesen, A
Bojesen, SE
Bolla, MK
Bonanni, B
Børresen-Dale, A-L
Brauch, H
Brennan, P
Brenner, H
Bruinsma, F
Brunet, J
Buhari, SA
Burwinkel, B
Butzow, R
Buys, SS
Cai, Q
Caldes, T
Campbell, I
Canniotto, R
Chang-Claude, J
Chiquette, J
Choi, J-Y
Claes, KBM
GEMO Study Collaborators,
Cook, LS
Cox, A
Cramer, DW
Cross, SS
Cybulski, C
Czene, K
Daly, MB
Damiola, F
Dansonka-Mieszkowska, A
Darabi, H
Dennis, J
Devilee, P
Diez, O
Doherty, JA
Domchek, SM
Dorfling, CM
Dörk, T
Dumont, M
Ehrencrona, H
Ejlertsen, B
Ellis, S
EMBRACE,
Engel, C
Lee, E
Evans, DG
Fasching, PA
Feliubadalo, L
Figueroa, J
Flesch-Janys, D
Fletcher, O
Flyger, H
Foretova, L
Fostira, F
Foulkes, WD
Fridley, BL
Friedman, E
Frost, D
Gambino, G
Ganz, PA
Garber, J
García-Closas, M
Gentry-Maharaj, A
Ghoussaini, M
Giles, GG
Glasspool, R
Godwin, AK
Goldberg, MS
Goldgar, DE
González-Neira, A
Goode, EL
Goodman, MT
Greene, MH
Gronwald, J
Guénel, P
Haiman, CA
Hall, P
Hallberg, E
Hamann, U
Hansen, TVO
Harrington, PA
Hartman, M
Hassan, N
Healey, S
Hereditary Breast and Ovarian Cancer Research Group Netherlands (HEBON),
Heitz, F
Herzog, J
Høgdall, E
Høgdall, CK
Hogervorst, FBL
Hollestelle, A
Hopper, JL
Hulick, PJ
Huzarski, T
Imyanitov, EN
KConFab Investigators,
Australian Ovarian Cancer Study Group,
Isaacs, C
Ito, H
Jakubowska, A
Janavicius, R
Jensen, A
John, EM
Johnson, N
Kabisch, M
Kang, D
Kapuscinski, M
Karlan, BY
Khan, S
Kiemeney, LA
Kjaer, SK
Knight, JA
Konstantopoulou, I
Kosma, V-M
Kristensen, V
Kupryjanczyk, J
Kwong, A
de la Hoya, M
Laitman, Y
Lambrechts, D
Le, N
De Leeneer, K
Lester, J
Levine, DA
Li, J
Lindblom, A
Long, J
Lophatananon, A
Loud, JT
Lu, K
Lubinski, J
Mannermaa, A
Manoukian, S
Le Marchand, L
Margolin, S
Marme, F
Massuger, LFAG
Matsuo, K
Mazoyer, S
McGuffog, L
McLean, C
McNeish, I
Meindl, A
Menon, U
Mensenkamp, AR
Milne, RL
Montagna, M
Moysich, KB
Muir, K
Mulligan, AM
Nathanson, KL
Ness, RB
Neuhausen, SL
Nevanlinna, H
Nord, S
Nussbaum, RL
Odunsi, K
Offit, K
Olah, E
Olopade, OI
Olson, JE
Olswold, C
O'Malley, D
Orlow, I
Orr, N
Osorio, A
Park, SK
Pearce, CL
Pejovic, T
Peterlongo, P
Pfeiler, G
Phelan, CM
Poole, EM
Pylkäs, K
Radice, P
Rantala, J
Rashid, MU
Rennert, G
Rhenius, V
Rhiem, K
Risch, HA
Rodriguez, G
Rossing, MA
Rudolph, A
Salvesen, HB
Sangrajrang, S
Sawyer, EJ
Schildkraut, JM
Schmidt, MK
Schmutzler, RK
Sellers, TA
Seynaeve, C
Shah, M
Shen, C-Y
Shu, X-O
Sieh, W
Singer, CF
Sinilnikova, OM
Slager, S
Song, H
Soucy, P
Southey, MC
Stenmark-Askmalm, M
Stoppa-Lyonnet, D
Sutter, C
Swerdlow, A
Tchatchou, S
Teixeira, MR
Teo, SH
Terry, KL
Terry, MB
Thomassen, M
Tibiletti, MG
Tihomirova, L
Tognazzo, S
Toland, AE
Tomlinson, I
Torres, D
Truong, T
Tseng, C-C
Tung, N
Tworoger, SS
Vachon, C
van den Ouweland, AMW
van Doorn, HC
van Rensburg, EJ
Van't Veer, LJ
Vanderstichele, A
Vergote, I
Vijai, J
Wang, Q
Wang-Gohrke, S
Weitzel, JN
Wentzensen, N
Whittemore, AS
Wildiers, H
Winqvist, R
Wu, AH
Yannoukakos, D
Yoon, S-Y
Yu, J-C
Zheng, W
Zheng, Y
Khanna, KK
Simard, J
Monteiro, AN
French, JD
Couch, FJ
Freedman, ML
Easton, DF
Dunning, AM
Pharoah, PD
Edwards, SL
Chenevix-Trench, G
Antoniou, AC
Gayther, SA
Dokumenttyp: Journal article
Erscheinungsdatum: 2016
Verlag/Hrsg.: NATURE PORTFOLIO
Schlagwörter: GEMO Study Collaborators / EMBRACE / Hereditary Breast and Ovarian Cancer Research Group Netherlands (HEBON) / KConFab Investigators / Australian Ovarian Cancer Study Group / Chromosomes / Human / Pair 19 / Humans / Breast Neoplasms / Ovarian Neoplasms / Genetic Predisposition to Disease / RNA / Messenger / Genotype / Polymorphism / Single Nucleotide / Alleles / African Continental Ancestry Group / Asian Continental Ancestry Group / Female / Genome-Wide Association Study
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-29177292
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : https://repository.icr.ac.uk/handle/internal/125

A locus at 19p13 is associated with breast cancer (BC) and ovarian cancer (OC) risk. Here we analyse 438 SNPs in this region in 46,451 BC and 15,438 OC cases, 15,252 BRCA1 mutation carriers and 73,444 controls and identify 13 candidate causal SNPs associated with serous OC (P=9.2 × 10(-20)), ER-negative BC (P=1.1 × 10(-13)), BRCA1-associated BC (P=7.7 × 10(-16)) and triple negative BC (P-diff=2 × 10(-5)). Genotype-gene expression associations are identified for candidate target genes ANKLE1 (P=2 × 10(-3)) and ABHD8 (P<2 × 10(-3)). Chromosome conformation capture identifies interactions between four candidate SNPs and ABHD8, and luciferase assays indicate six risk alleles increased transactivation of the ADHD8 promoter. Targeted deletion of a region containing risk SNP rs56069439 in a putative enhancer induces ANKLE1 downregulation; and mRNA stability assays indicate functional effects for an ANKLE1 3'-UTR SNP. Altogether, these data suggest that multiple SNPs at 19p13 regulate ABHD8 and perhaps ANKLE1 expression, and indicate common mechanisms underlying breast and ovarian cancer risk.