التفاصيل البيبلوغرافية
| العنوان: |
Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk |
| المؤلفون: |
Gaudet, M. M., Kuchenbaecker, K. B., Vijai, J., Klein, R. J., Kirchhoff, T., McGuffog, L., Barrowdale, D., Dunning, A. M., Lee, A., Dennis, J., Healey, S., Dicks, E., Soucy, P., Sinilnikova, O. M., Pankratz, V. S., Wang, X., Eldridge, R. C., Tessier, D. C., Vincent, D., Bacot, F., Hogervorst, F. B. L., Peock, S., Stoppa-Lyonnet, D., Coulet, F., Colas, C., Soubrier, F., Peterlongo, P., Schmutzler, R. K., Nathanson, K. L., Piedmonte, M., Singer, C. F., Thomassen, M., Sokolowska, J., Bronner, M., Hansen, T. V. O., Neuhausen, S. L., Blanco, I., Greene, M. H., Garber, J., Weitzel, J. N., Andrulis, I. L., Goldgar, D. E., D'Andrea, E., Caldes, T., Nevanlinna, H., Osorio, A., van Rensburg, E. J., Arason, A., Rennert, G., van den Ouweland, A. M. W., van der Hout, A. H., Kets, C. M., Aalfs, C. M., Wijnen, J. T., Ausems, M. G. E. M., Frost, D., Ellis, S., Fineberg, E., Platte, R., Evans, D. G., Jacobs, C., Adlard, J., Tischkowitz, M., Porteous, M. E., Damiola, F., Golmard, L., Barjhoux, L., Longy, M., Belotti, M., Ferrer, S. F., Mazoyer, S., Spurdle, A. B., Manoukian, S., Barile, M., Genuardi, M., Arnold, N., Meindl, A., Sutter, C., Wappenschmidt, B., Domchek, S. M., Pfeiler, G., Friedman, E., Jensen, U. B., Robson, M., Shah, S., Lazaro, C., Mai, P. L., Benitez, J., Southey, M. C., Schmidt, M. K., Fasching, P. A., Peto, J., Humphreys, M. K., Wang, Q., Michailidou, K., Sawyer, E. J., Burwinkel, B., Guénel, P., Bojesen, S. E., Milne, R. L., Brenner, H., Lochmann, M., Brauch, H., Ko, Y-D., Baisch, C., Fischer, H-P., Bruening, T., Pesch, B., Rabstein, S., Spickenheuer, A., Aittomäki, K., Dörk, T., Margolin, S., Mannermaa, A., Lambrechts, D., Chang-Claude, J., Radice, P., Giles, G. G., Haiman, C. A., Winqvist, R., Devillee, P., García-Closas, M., Schoof, N., Hooning, M. J., Cox, A., Pharoah, P. D. P., Jakubowska, A., Orr, N., González-Neira, A., Pita, G., Alonso, M. R., Hall, P., Couch, F. J., Simard, J., Altshuler, D., Easton, D. F., Chenevix-Trench, G., Antoniou, A. C., Offit, K., Rookus, M. A., van Leeuwen, F. E., Verhoef, S., de Lange, J. L., Collée, J. M., Seynaeve, C., van Deurzen, C. H. M., van Asperen, C. J., Tollenaar, R. A., Devilee, P., van Cronenburg, T. C. T. E. F., Mensenkamp, A. R., van der Luijt, R. B., van Os, T. A. M., Gille, J. J. P., Waisfisz, Q., Meijers-Heijboer, H. E. J., Gómez-Garcia, E. B., Blok, M. J., Oosterwijk, J. C., Mourits, M. J., de Bock, G. H., Vasen, H. F., Miedzybrodzka, Z., Gregory, H., Morrison, P., Jeffers, L., Cole, T., Ong, K-R., Hoffman, J., Donaldson, A., James, M., Paterson, J., Taylor, A., Murray, A., Rogers, M. T., McCann, E., Kennedy, M. J., Barton, D., Porteous, M., Drummond, S., Brewer, C., Kivuva, E., Searle, A., Goodman, S., Hill, K., Davidson, R., Murday, V., Bradshaw, N., Snadden, L., Longmuir, M., Watt, C., Gibson, S., Haque, E., Tobias, E., Duncan, A., Izatt, L., Langman, C., Brady, A., Dorkins, H., Melville, A., Randhawa, K., Barwell, J., Serra-Feliu, G., Ellis, I., Houghton, C., Lalloo, F., Taylor, J., Side, L., Male, A., Berlin, C., Eason, J., Collier, R., Douglas, F., Claber, O., Jobson, I., Walker, L., McLeod, D., Halliday, D., Durell, S., Stayner, B., Eeles, R. A., Shanley, S., Rahman, N., Houlston, R., Bancroft, E., Page, E., Ardern-Jones, A., Kohut, K., Wiggins, J., Castro, E., Killick, E., Martin, S., Rea, G., Kulkarni, A., Cook, J., Quarrell, O., Bardsley, C., Hodgson, S., Goff, S., Brice, G., Winchester, L., Eddy, C., Tripathi, V., Attard, V., Lehmann, A., Eccles, D., Lucassen, A., Crawford, G., McBride, D., Smalley, S., Sinilnikova, O., Verny-Pierre, C., Giraud, S., Léone, M., Gauthier-Villars, M., Buecher, B., Houdayer, C., Moncoutier, V., Tirapo, C., de Pauw, A., Bressac-de-Paillerets, B., Caron, O., Bignon, Y-J., Uhrhammer, N., Lasset, C., Bonadona, V., Handallou, S., Hardouin, A., Berthet, P., Sobol, H., Bourdon, V., Noguchi, T., Remenieras, A., Eisinger, F., Coupier, I., Pujol, P., Peyrat, J-P., Fournier, J., Révillion, F., Vennin, P., Adenis, C., Rouleau, E., Lidereau, R., Demange, L., Nogues, C., Muller, D., Fricker, J-P., Barouk-Simonet, E., Bonnet, F., Bubien, V., Sevenet, N., Toulas, C., Guimbaud, R., Gladieff, L., Feillel, V., Dreyfus, H., Rebischung, C., Peysselon, M., Coron, F., Faivre, L., Prieur, F., Lebrun, M., Kientz, C., Frénay, M., Vénat-Bouvet, L., Delnatte, C., Mortemousque, I., Lynch, H. T., Snyder, C. L. |
| بيانات النشر: |
Public Library of Science |
| سنة النشر: |
2016 |
| المجموعة: |
University of Leicester: Leicester Research Archive (LRA) |
| مصطلحات موضوعية: |
Breast cancer, Genome-wide association studies, Mutation, Variant genotypes, Genetic loci, Consortia, Mutation detection, Genotyping |
| الوصف: |
Common genetic variants contribute to the observed variation in breast cancer risk for BRCA2 mutation carriers; those known to date have all been found through population-based genome-wide association studies (GWAS). To comprehensively identify breast cancer risk modifying loci for BRCA2 mutation carriers, we conducted a deep replication of an ongoing GWAS discovery study. Using the ranked P-values of the breast cancer associations with the imputed genotype of 1.4 M SNPs, 19,029 SNPs were selected and designed for inclusion on a custom Illumina array that included a total of 211,155 SNPs as part of a multi-consortial project. DNA samples from 3,881 breast cancer affected and 4,330 unaffected BRCA2 mutation carriers from 47 studies belonging to the Consortium of Investigators of Modifiers of BRCA1/2 were genotyped and available for analysis. We replicated previously reported breast cancer susceptibility alleles in these BRCA2 mutation carriers and for several regions (including FGFR2, MAP3K1, CDKN2A/B, and PTHLH) identified SNPs that have stronger evidence of association than those previously published. We also identified a novel susceptibility allele at 6p24 that was inversely associated with risk in BRCA2 mutation carriers (rs9348512; per allele HR = 0.85, 95% CI 0.80-0.90, P = 3.9×10 -8 ). This SNP was not associated with breast cancer risk either in the general population or in BRCA1 mutation carriers. The locus lies within a region containing TFAP2A, which encodes a transcriptional activation protein that interacts with several tumor suppressor genes. This report identifies the first breast cancer risk locus specific to a BRCA2 mutation background. This comprehensive update of novel and previously reported breast cancer susceptibility loci contributes to the establishment of a panel of SNPs that modify breast cancer risk in BRCA2 mutation carriers. This panel may have clinical utility for women with BRCA2 mutations weighing options for medical prevention of breast cancer. ; Peer-reviewed ; Publisher Version |
| نوع الوثيقة: |
article in journal/newspaper |
| اللغة: |
English |
| تدمد: |
1553-7390
1553-7404 |
| العلاقة: |
PLoS Genetics, 2013, 9 (3), e1003173; http://journals.plos.org/plosgenetics/article?id=10.1371/journal.pgen.1003173Test; http://hdl.handle.net/2381/37295Test |
| DOI: |
10.1371/journal.pgen.1003173 |
| الإتاحة: |
https://doi.org/10.1371/journal.pgen.1003173Test
http://journals.plos.org/plosgenetics/article?id=10.1371/journal.pgen.1003173Test
http://hdl.handle.net/2381/37295Test |
| حقوق: |
This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication. |
| رقم الانضمام: |
edsbas.9E60DC6D |
| قاعدة البيانات: |
BASE |
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