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DOI 10.1038/sj.bjc.6605416

Медицинская библиотека · British journal of cancer · 2009

Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA).

Osorio A, Milne R L, Pita G, Peterlongo P, Heikkinen T, Simard J, Chenevix-Trench G, Spurdle A B, Beesley J, Chen X, Healey S, KConFab, Neuhausen S L, Ding Y C, Couch F J, Wang X, Lindor N, Manoukian S, Barile M, Viel A, Tizzoni L, Szabo C I, Foretova L, Zikan M, Claes K, Greene M H, Mai P, Rennert G, Lejbkowicz F, Barnett-Griness O, Andrulis I L, Ozcelik H, Weerasooriya N, OCGN, Gerdes A-M, Thomassen M, Cruger D G, Caligo M A, Friedman E, Kaufman B, Laitman Y, Cohen S, Kontorovich T, Gershoni-Baruch R, Dagan E, Jernström H, Askmalm M S, Arver B, Malmer B, SWE-BRCA, Domchek S M, Nathanson K L, Brunet J, Ramón Y Cajal T, Yannoukakos D, Hamann U, HEBON, Hogervorst F B L, Verhoef S, Gómez García E B, Wijnen J T, van den Ouweland A, EMBRACE, Easton D F, Peock S, Cook M, Oliver C T, Frost D, Luccarini C, Evans D G, Lalloo F, Eeles R, Pichert G, Cook J, Hodgson S, Morrison P J, Douglas F, Godwin A K, GEMO, Sinilnikova O M, Barjhoux L, Stoppa-Lyonnet D, Moncoutier V, Giraud S, Cassini C, Olivier-Faivre L, Révillion F, Peyrat J-P, Muller D, Fricker J-P, Lynch H T, John E M, Buys S, Daly M, Hopper J L, Terry M B, Miron A, Yassin Y, Goldgar D, Breast Cancer Family Registry, Singer C F, Gschwantler-Kaulich D, Pfeiler G, Spiess A-C, Hansen Thomas V O, Johannsson O T, Kirchhoff T, Offit K, Kosarin K, Piedmonte M, Rodriguez G C, Wakeley K, Boggess J F, Basil J, Schwartz P E, Blank S V, Toland A E, Montagna M, Casella C, Imyanitov E N, Allavena A, Schmutzler R K, Versmold B, Engel C, Meindl A, Ditsch N, Arnold N, Niederacher D, Deissler H, Fiebig B, Varon-Mateeva R, Schaefer D, Froster U G, Caldes T, de la Hoya M, McGuffog L, Antoniou A C, Nevanlinna H, Radice P, Benítez J, CMBA

СтатьяПоддержка NIH: внешняя программаResearch Support, N.I.H., IntramuralПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

In this study we aimed to evaluate the role of a SNP in intron 1 of the ERCC4 gene (rs744154), previously reported to be associated with a reduced risk of breast cancer in the general population, as a breast cancer risk modifier in BRCA1 and BRCA2 mutation carriers.

METHODS

We have genotyped rs744154 in 9408 BRCA1 and 5632 BRCA2 mutation carriers from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA) and assessed its association with breast cancer risk using a retrospective weighted cohort approach.

RESULTS

We found no evidence of association with breast cancer risk for BRCA1 (per-allele HR: 0.98, 95% CI: 0.93-1.04, P = 0.5) or BRCA2 (per-allele HR: 0.97, 95% CI: 0.89-1.06, P = 0.5) mutation carriers.

CONCLUSION

This SNP is not a significant modifier of breast cancer risk for mutation carriers, though weak associations cannot be ruled out.

Для цитирования: Osorio A, Milne R L, Pita G, Peterlongo P, Heikkinen T, Simard J, Chenevix-Trench G, Spurdle A B, Beesley J, Chen X, Healey S, KConFab, Neuhausen S L, Ding Y C, Couch F J, Wang X, Lindor N, Manoukian S, Barile M, Viel A, Tizzoni L, Szabo C I, Foretova L, Zikan M, Claes K, Greene M H, Mai P, Rennert G, Lejbkowicz F, Barnett-Griness O, Andrulis I L, Ozcelik H, Weerasooriya N, OCGN, Gerdes A-M, Thomassen M, Cruger D G, Caligo M A, Friedman E, Kaufman B, Laitman Y, Cohen S, Kontorovich T, Gershoni-Baruch R, Dagan E, Jernström H, Askmalm M S, Arver B, Malmer B, SWE-BRCA, Domchek S M, Nathanson K L, Brunet J, Ramón Y Cajal T, Yannoukakos D, Hamann U, HEBON, Hogervorst F B L, Verhoef S, Gómez García E B, Wijnen J T, van den Ouweland A, EMBRACE, Easton D F, Peock S, Cook M, Oliver C T, Frost D, Luccarini C, Evans D G, Lalloo F, Eeles R, Pichert G, Cook J, Hodgson S, Morrison P J, Douglas F, Godwin A K, GEMO, Sinilnikova O M, Barjhoux L, Stoppa-Lyonnet D, Moncoutier V, Giraud S, Cassini C, Olivier-Faivre L, Révillion F, Peyrat J-P, Muller D, Fricker J-P, Lynch H T, John E M, Buys S, Daly M, Hopper J L, Terry M B, Miron A, Yassin Y, Goldgar D, Breast Cancer Family Registry, Singer C F, Gschwantler-Kaulich D, Pfeiler G, Spiess A-C, Hansen Thomas V O, Johannsson O T, Kirchhoff T, Offit K, Kosarin K, Piedmonte M, Rodriguez G C, Wakeley K, Boggess J F, Basil J, Schwartz P E, Blank S V, Toland A E, Montagna M, Casella C, Imyanitov E N, Allavena A, Schmutzler R K, Versmold B, Engel C, Meindl A, Ditsch N, Arnold N, Niederacher D, Deissler H, Fiebig B, Varon-Mateeva R, Schaefer D, Froster U G, Caldes T, de la Hoya M, McGuffog L, Antoniou A C, Nevanlinna H, Radice P, Benítez J, CMBA. Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA).. British journal of cancer. 2009. DOI: 10.1038/sj.bjc.6605416.

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