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AURKA F31I polymorphism and breast cancer risk in BRCA1 and BRCA2 mutation carriers: A consortium of investigators of modifiers of BRCA1/2 study

Couch, Fergus J. (author)
Sinilnikova, Olga (author)
Vierkant, Robert A. (author)
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Pankratz, V. Shane (author)
Fredericksen, Zachary S. (author)
Stoppa-Lyonnet, Dominique (author)
Coupier, Isabelle (author)
Hughes, David (author)
Hardouin, Agnes (author)
Berthet, Pascaline (author)
Peock, Susan (author)
Cook, Margaret (author)
Baynes, Caroline (author)
Hodgson, Shirley (author)
Morrison, Patrick J. (author)
Porteous, Mary E. (author)
Jakubowska, Anna (author)
Lubinski, Jan (author)
Gronwald, Jacek (author)
Spurdle, Amanda B. (author)
kConFab, [unknown] (author)
Schmutzler, Rita (author)
Versmold, Beatrix (author)
Engel, Christoph (author)
Meindl, Alfons (author)
Sutter, Christian (author)
Horst, Jurgen (author)
Schaefer, Dieter (author)
Offit, Kenneth (author)
Kirchhoff, Tomas (author)
Andrulis, Irene L. (author)
Ilyushik, Eduard (author)
Glendon, Gordon (author)
Devilee, Peter (author)
Vreeswijk, Maaike P. G. (author)
Vasen, Hans F. A. (author)
Borg, Åke (author)
Lund University,Lunds universitet,Bröstcancer-genetik,Sektion I,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Breastcancer-genetics,Section I,Department of Clinical Sciences, Lund,Faculty of Medicine
Harbst, Katja (author)
Lund University,Lunds universitet,Bröstcancer-genetik,Sektion I,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Breastcancer-genetics,Section I,Department of Clinical Sciences, Lund,Faculty of Medicine
Struewing, Jeffery P. (author)
Greene, Mark H. (author)
Neuhausen, Susan L. (author)
Rebbeck, Timothy R. (author)
Nathanson, Katherine (author)
Domchek, Susan (author)
Wagner, Theresa (author)
Garber, Judy E. (author)
Szabo, Csilla (author)
Zikan, Michal (author)
Foretova, Lenka (author)
Olson, Janet E. (author)
Sellers, Thomas A. (author)
Lindor, Noralane (author)
Ll, Heli Nevanlinna (author)
Tommiska, Johanna (author)
Aittomaki, Kristiina (author)
Hamann, Ute (author)
Rashid, Muhammad U. (author)
Torres, Diana (author)
Simard, Jacques (author)
Durocher, Francine (author)
Guenard, Frederic (author)
Lynch, Henry T. (author)
Isaacs, Claudine (author)
Weitzel, Jeffrey (author)
Olopade, Olufunmilayo I. (author)
Narod, Steven (author)
Daly, Mary B. (author)
Godwin, Andrew K. (author)
Tomlinson, Gail (author)
Easton, Douglas F. (author)
Chenevix-Trench, Georgia (author)
Antoniou, Antonis C. (author)
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 (creator_code:org_t)
2007
2007
English.
In: Cancer Epidemiology Biomarkers & Prevention. - 1538-7755. ; 16:7, s. 1416-1421
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The AURKA oncogene is associated with abnormal chromosome segregation and aneuploidy and predisposition to cancer. Amplification of AURKA has been detected at higher frequency in tumors from BRCA1 and BRCA2 mutation carriers than in sporadic breast tumors, suggesting that overexpression of AURKA and inactivation of BRCA1 and BRCA2 cooperate during tumor development and progression. The F31I polymorphism in AURKA has been associated with breast cancer risk in the homozygous state in prior studies. We evaluated whether the AURKA F31I polymorphism modifies breast cancer risk in BRCA1 and BRCA2 mutation carriers from the Consortium of Investigators of Modifiers of BRCA1/2. Consortium of Investigators of Modifiers of BRCA1/2 was established to provide sufficient statistical power through increased numbers of mutation carriers to identify polymorphisms that act as modifiers of cancer risk and can refine breast cancer risk estimates in BRCA1 and BRCA2 mutation carriers. A total of 4,935 BRCA1 and 2,241 BRCA2 mutation carriers and 11 individuals carrying both BRCA1 and BRCA2 mutations was genotyped for F31I. Overall, homozygosity for the 311 allele was not significantly associated with breast cancer risk in BRCA1 and BRCA2 carriers combined [hazard ratio (HR), 0.91; 95% confidence interval (95% CI), 0.77-1.061. Similarly, no significant association was seen in BRCA1 (HR, 0.90; 95% Cl, 0.75-1.08) or BRCA2 carriers (HR, 0.93; 95% CI, 0.67-1.29) or when assessing the modifying effects of either bilateral prophylactic oophorectomy or menopausal status of BRCA1 and BRCA2 carriers. In summary, the F31I polymorphism in AURKA is not associated with a modified risk of breast cancer in BRCA1 and BRCA2 carriers.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

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By the author/editor
Couch, Fergus J.
Sinilnikova, Olg ...
Vierkant, Robert ...
Pankratz, V. Sha ...
Fredericksen, Za ...
Stoppa-Lyonnet, ...
show more...
Coupier, Isabell ...
Hughes, David
Hardouin, Agnes
Berthet, Pascali ...
Peock, Susan
Cook, Margaret
Baynes, Caroline
Hodgson, Shirley
Morrison, Patric ...
Porteous, Mary E ...
Jakubowska, Anna
Lubinski, Jan
Gronwald, Jacek
Spurdle, Amanda ...
kConFab, [unknow ...
Schmutzler, Rita
Versmold, Beatri ...
Engel, Christoph
Meindl, Alfons
Sutter, Christia ...
Horst, Jurgen
Schaefer, Dieter
Offit, Kenneth
Kirchhoff, Tomas
Andrulis, Irene ...
Ilyushik, Eduard
Glendon, Gordon
Devilee, Peter
Vreeswijk, Maaik ...
Vasen, Hans F. A ...
Borg, Åke
Harbst, Katja
Struewing, Jeffe ...
Greene, Mark H.
Neuhausen, Susan ...
Rebbeck, Timothy ...
Nathanson, Kathe ...
Domchek, Susan
Wagner, Theresa
Garber, Judy E.
Szabo, Csilla
Zikan, Michal
Foretova, Lenka
Olson, Janet E.
Sellers, Thomas ...
Lindor, Noralane
Ll, Heli Nevanli ...
Tommiska, Johann ...
Aittomaki, Krist ...
Hamann, Ute
Rashid, Muhammad ...
Torres, Diana
Simard, Jacques
Durocher, Franci ...
Guenard, Frederi ...
Lynch, Henry T.
Isaacs, Claudine
Weitzel, Jeffrey
Olopade, Olufunm ...
Narod, Steven
Daly, Mary B.
Godwin, Andrew K ...
Tomlinson, Gail
Easton, Douglas ...
Chenevix-Trench, ...
Antoniou, Antoni ...
show less...
About the subject
MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
and Clinical Medicin ...
and Cancer and Oncol ...
Articles in the publication
Cancer Epidemiol ...
By the university
Lund University

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