Pelttari, L. M., Khan, S., Vuorela, M., Kiiski, J. I., Vilske, S., Nevanlinna, V., Ranta, S., Schleutker, J., Winqvist, R., Kallioniemi, A., Dörk, T., Bogdanova, N. V., Figueroa, J., Pharoah, P. D. P., Schmidt, M. K., Dunning, A. M., García-Closas, M., Bolla, M. K., Dennis, J., ... kConFab/AOCS Investigators (2016). RAD51B in Familial Breast Cancer. PLOS ONE, 11(5), Artikel e0153788. https://doi.org/10.1371/journal.pone.0153788
Pelttari, LM, Khan, S, Vuorela, M, Kiiski, JI, Vilske, S, Nevanlinna, V, Ranta, S, Schleutker, J, Winqvist, R, Kallioniemi, A, Dörk, T, Bogdanova, NV, Figueroa, J, Pharoah, PDP, Schmidt, MK, Dunning, AM, García-Closas, M, Bolla, MK, Dennis, J, Michailidou, K, Wang, Q, Hopper, JL, Southey, MC, Rosenberg, EH, Fasching, PA, Beckmann, MW, Peto, J, Dos-Santos-Silva, I, Sawyer, EJ, Tomlinson, I, Burwinkel, B, Surowy, H, Guénel, P, Truong, T, Bojesen, SE, Nordestgaard, BG, Benitez, J, González-Neira, A, Neuhausen, SL, Anton-Culver, H, Brenner, H, Arndt, V, Meindl, A, Schmutzler, RK, Brauch, H, Brüning, T, Lindblom, A, Margolin, S, Mannermaa, A, Hartikainen, JM & kConFab/AOCS Investigators 2016, 'RAD51B in Familial Breast Cancer', PLOS ONE, bind 11, nr. 5, e0153788. https://doi.org/10.1371/journal.pone.0153788
@article{896ad2c8d81244a49282a7c7780d3981,
title = "RAD51B in Familial Breast Cancer",
abstract = "Common variation on 14q24.1, close to RAD51B, has been associated with breast cancer: rs999737 and rs2588809 with the risk of female breast cancer and rs1314913 with the risk of male breast cancer. The aim of this study was to investigate the role of RAD51B variants in breast cancer predisposition, particularly in the context of familial breast cancer in Finland. We sequenced the coding region of RAD51B in 168 Finnish breast cancer patients from the Helsinki region for identification of possible recurrent founder mutations. In addition, we studied the known rs999737, rs2588809, and rs1314913 SNPs and RAD51B haplotypes in 44,791 breast cancer cases and 43,583 controls from 40 studies participating in the Breast Cancer Association Consortium (BCAC) that were genotyped on a custom chip (iCOGS). We identified one putatively pathogenic missense mutation c.541C>T among the Finnish cancer patients and subsequently genotyped the mutation in additional breast cancer cases (n = 5259) and population controls (n = 3586) from Finland and Belarus. No significant association with breast cancer risk was seen in the meta-analysis of the Finnish datasets or in the large BCAC dataset. The association with previously identified risk variants rs999737, rs2588809, and rs1314913 was replicated among all breast cancer cases and also among familial cases in the BCAC dataset. The most significant association was observed for the haplotype carrying the risk-alleles of all the three SNPs both among all cases (odds ratio (OR): 1.15, 95% confidence interval (CI): 1.11-1.19, P = 8.88 × 10-16) and among familial cases (OR: 1.24, 95% CI: 1.16-1.32, P = 6.19 × 10-11), compared to the haplotype with the respective protective alleles. Our results suggest that loss-of-function mutations in RAD51B are rare, but common variation at the RAD51B region is significantly associated with familial breast cancer risk.",
keywords = "Journal Article",
author = "Pelttari, {Liisa M} and Sofia Khan and Mikko Vuorela and Kiiski, {Johanna I} and Sara Vilske and Viivi Nevanlinna and Salla Ranta and Johanna Schleutker and Robert Winqvist and Anne Kallioniemi and Thilo D{\"o}rk and Bogdanova, {Natalia V} and Jonine Figueroa and Pharoah, {Paul D P} and Schmidt, {Marjanka K} and Dunning, {Alison M} and Montserrat Garc{\'i}a-Closas and Bolla, {Manjeet K} and Joe Dennis and Kyriaki Michailidou and Qin Wang and Hopper, {John L} and Southey, {Melissa C} and Rosenberg, {Efraim H} and Fasching, {Peter A} and Beckmann, {Matthias W} and Julian Peto and Isabel Dos-Santos-Silva and Sawyer, {Elinor J} and Ian Tomlinson and Barbara Burwinkel and Harald Surowy and Pascal Gu{\'e}nel and Th{\'e}r{\`e}se Truong and Bojesen, {Stig E} and Nordestgaard, {B{\o}rge G} and Javier Benitez and Anna Gonz{\'a}lez-Neira and Neuhausen, {Susan L} and Hoda Anton-Culver and Hermann Brenner and Volker Arndt and Alfons Meindl and Schmutzler, {Rita K} and Hiltrud Brauch and Thomas Br{\"u}ning and Annika Lindblom and Sara Margolin and Arto Mannermaa and Hartikainen, {Jaana M} and {kConFab/AOCS Investigators}",
year = "2016",
doi = "10.1371/journal.pone.0153788",
language = "English",
volume = "11",
journal = "PLOS ONE",
issn = "1932-6203",
publisher = "Public Library of Science",
number = "5",
}
TY - JOUR
T1 - RAD51B in Familial Breast Cancer
AU - Pelttari, Liisa M
AU - Khan, Sofia
AU - Vuorela, Mikko
AU - Kiiski, Johanna I
AU - Vilske, Sara
AU - Nevanlinna, Viivi
AU - Ranta, Salla
AU - Schleutker, Johanna
AU - Winqvist, Robert
AU - Kallioniemi, Anne
AU - Dörk, Thilo
AU - Bogdanova, Natalia V
AU - Figueroa, Jonine
AU - Pharoah, Paul D P
AU - Schmidt, Marjanka K
AU - Dunning, Alison M
AU - García-Closas, Montserrat
AU - Bolla, Manjeet K
AU - Dennis, Joe
AU - Michailidou, Kyriaki
AU - Wang, Qin
AU - Hopper, John L
AU - Southey, Melissa C
AU - Rosenberg, Efraim H
AU - Fasching, Peter A
AU - Beckmann, Matthias W
AU - Peto, Julian
AU - Dos-Santos-Silva, Isabel
AU - Sawyer, Elinor J
AU - Tomlinson, Ian
AU - Burwinkel, Barbara
AU - Surowy, Harald
AU - Guénel, Pascal
AU - Truong, Thérèse
AU - Bojesen, Stig E
AU - Nordestgaard, Børge G
AU - Benitez, Javier
AU - González-Neira, Anna
AU - Neuhausen, Susan L
AU - Anton-Culver, Hoda
AU - Brenner, Hermann
AU - Arndt, Volker
AU - Meindl, Alfons
AU - Schmutzler, Rita K
AU - Brauch, Hiltrud
AU - Brüning, Thomas
AU - Lindblom, Annika
AU - Margolin, Sara
AU - Mannermaa, Arto
AU - Hartikainen, Jaana M
AU - kConFab/AOCS Investigators
PY - 2016
Y1 - 2016
N2 - Common variation on 14q24.1, close to RAD51B, has been associated with breast cancer: rs999737 and rs2588809 with the risk of female breast cancer and rs1314913 with the risk of male breast cancer. The aim of this study was to investigate the role of RAD51B variants in breast cancer predisposition, particularly in the context of familial breast cancer in Finland. We sequenced the coding region of RAD51B in 168 Finnish breast cancer patients from the Helsinki region for identification of possible recurrent founder mutations. In addition, we studied the known rs999737, rs2588809, and rs1314913 SNPs and RAD51B haplotypes in 44,791 breast cancer cases and 43,583 controls from 40 studies participating in the Breast Cancer Association Consortium (BCAC) that were genotyped on a custom chip (iCOGS). We identified one putatively pathogenic missense mutation c.541C>T among the Finnish cancer patients and subsequently genotyped the mutation in additional breast cancer cases (n = 5259) and population controls (n = 3586) from Finland and Belarus. No significant association with breast cancer risk was seen in the meta-analysis of the Finnish datasets or in the large BCAC dataset. The association with previously identified risk variants rs999737, rs2588809, and rs1314913 was replicated among all breast cancer cases and also among familial cases in the BCAC dataset. The most significant association was observed for the haplotype carrying the risk-alleles of all the three SNPs both among all cases (odds ratio (OR): 1.15, 95% confidence interval (CI): 1.11-1.19, P = 8.88 × 10-16) and among familial cases (OR: 1.24, 95% CI: 1.16-1.32, P = 6.19 × 10-11), compared to the haplotype with the respective protective alleles. Our results suggest that loss-of-function mutations in RAD51B are rare, but common variation at the RAD51B region is significantly associated with familial breast cancer risk.
AB - Common variation on 14q24.1, close to RAD51B, has been associated with breast cancer: rs999737 and rs2588809 with the risk of female breast cancer and rs1314913 with the risk of male breast cancer. The aim of this study was to investigate the role of RAD51B variants in breast cancer predisposition, particularly in the context of familial breast cancer in Finland. We sequenced the coding region of RAD51B in 168 Finnish breast cancer patients from the Helsinki region for identification of possible recurrent founder mutations. In addition, we studied the known rs999737, rs2588809, and rs1314913 SNPs and RAD51B haplotypes in 44,791 breast cancer cases and 43,583 controls from 40 studies participating in the Breast Cancer Association Consortium (BCAC) that were genotyped on a custom chip (iCOGS). We identified one putatively pathogenic missense mutation c.541C>T among the Finnish cancer patients and subsequently genotyped the mutation in additional breast cancer cases (n = 5259) and population controls (n = 3586) from Finland and Belarus. No significant association with breast cancer risk was seen in the meta-analysis of the Finnish datasets or in the large BCAC dataset. The association with previously identified risk variants rs999737, rs2588809, and rs1314913 was replicated among all breast cancer cases and also among familial cases in the BCAC dataset. The most significant association was observed for the haplotype carrying the risk-alleles of all the three SNPs both among all cases (odds ratio (OR): 1.15, 95% confidence interval (CI): 1.11-1.19, P = 8.88 × 10-16) and among familial cases (OR: 1.24, 95% CI: 1.16-1.32, P = 6.19 × 10-11), compared to the haplotype with the respective protective alleles. Our results suggest that loss-of-function mutations in RAD51B are rare, but common variation at the RAD51B region is significantly associated with familial breast cancer risk.
KW - Journal Article
U2 - 10.1371/journal.pone.0153788
DO - 10.1371/journal.pone.0153788
M3 - Journal article
C2 - 27149063
SN - 1932-6203
VL - 11
JO - PLOS ONE
JF - PLOS ONE
IS - 5
M1 - e0153788
ER -
