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19p13.1 is a triple...
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Stevens, Kristen N
(author)
19p13.1 is a triple negative-specific breast cancer susceptibility locus
- Article/chapterEnglish2012
Publisher, publication year, extent ...
Numbers
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LIBRIS-ID:oai:DiVA.org:uu-171130
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https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-171130URI
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https://doi.org/10.1158/0008-5472.CAN-11-3364DOI
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http://kipublications.ki.se/Default.aspx?queryparsed=id:124381503URI
Supplementary language notes
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Language:English
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Summary in:English
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Classification
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Subject category:ref swepub-contenttype
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Subject category:art swepub-publicationtype
Notes
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The 19p13.1 breast cancer susceptibility locus is a modifier of breast cancer risk in BRCA1 mutation carriers and is also associated with risk of ovarian cancer. Here we investigated 19p13.1 variation and risk of breast cancer subtypes, defined by estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor-2 (HER2) status, using 48,869 breast cancer cases and 49,787 controls from the Breast Cancer Association Consortium (BCAC). Variants from 19p13.1 were not associated with breast cancer overall or with ER-positive breast cancer but were significantly associated with ER-negative breast cancer risk [rs8170 Odds Ratio (OR)=1.10, 95% Confidence Interval (CI) 1.05 - 1.15, p=3.49 x 10-5] and triple negative (TN) (ER, PR and HER2 negative) breast cancer [rs8170 OR=1.22, 95% CI 1.13 - 1.31, p=2.22 x 10-7]. However, rs8170 was no longer associated with ER-negative breast cancer risk when TN cases were excluded [OR=0.98, 95% CI 0.89 - 1.07, p=0.62]. In addition, a combined analysis of TN cases from BCAC and the Triple Negative Breast Cancer Consortium (TNBCC) (n=3,566) identified a genome-wide significant association between rs8170 and TN breast cancer risk [OR=1.25, 95% CI 1.18 - 1.33, p=3.31 x 10-13]. Thus, 19p13.1 is the first triple negative-specific breast cancer risk locus and the first locus specific to a histological subtype defined by ER, PR, and HER2 to be identified. These findings provide convincing evidence that genetic susceptibility to breast cancer varies by tumor subtype and that triple negative tumors and other subtypes likely arise through distinct etiologic pathways.
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Fredericksen, Zachary
(author)
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Vachon, Celine M
(author)
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Wang, Xianshu
(author)
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Margolin, SaraKarolinska Institutet
(author)
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Lindblom, AnnikaKarolinska Institutet
(author)
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Nevanlinna, Heli
(author)
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Greco, Dario
(author)
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Aittomäki, Kristiina
(author)
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Blomqvist, CarlUppsala universitet,Enheten för onkologi(Swepub:uu)carlblom
(author)
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Chang-Claude, Jenny
(author)
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Vrieling, Alina
(author)
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Flesch-Janys, Dieter
(author)
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Sinn, Hans-Peter
(author)
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Wang-Gohrke, Shan
(author)
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Nickels, Stefan
(author)
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Brauch, Hiltrud
(author)
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Ko, Yon-Dschun
(author)
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Fischer, Hans-Peter
(author)
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Network, The Genica
(author)
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Schmutzler, Rita K
(author)
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Meindl, Alfons
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Bartram, Claus R
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Schott, Sarah
(author)
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Engel, Christoph
(author)
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Godwin, Andrew K
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Weaver, Joellen
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Pathak, Harsh B
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Sharma, Priyanka
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Brenner, Hermann
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Muller, Heiko
(author)
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Arndt, Volker
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Stegmaier, Christa
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Miron, Penelope
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Yannoukakos, Drakoulis
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Stavropoulou, Alexandra
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Fountzilas, George
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Gogas, Helen J
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Swann, Ruth
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Dwek, Miriam
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Perkins, Katherine Anne
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Milne, Roger L
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Benítez, Javier
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Zamora, M Pilar
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Ignacio Arias Pérez, José
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Bojesen, Stig E
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Nielsen, Sune F
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Nordestgaard, Borge G
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Flyger, Henrik
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Guénel, Pascal
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Truong, Thérèse
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Menegaux, Florence
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Cordina-Duverger, Emilie
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Burwinkel, Barbara
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Marmé, Frederick
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Schneeweiss, Andreas
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Sohn, Christof
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Sawyer, Elinor
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Tomlinson, Ian
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Kerin, Michael J
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Peto, Julian
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Johnson, Nichola
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Ekici, Arif B
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Lophatananon, Artitaya
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Puttawibul, PuttisakKarolinska Institutet
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Czene, KamilaKarolinska Institutet
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Ademuyiwa, Foluso
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Seynaeve, Caroline
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Couch, Fergus J
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Karolinska InstitutetEnheten för onkologi
(creator_code:org_t)
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In:Cancer Research72, s. 1795-0008-54721538-7445
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- By the author/editor
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Stevens, Kristen ...
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Fredericksen, Za ...
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Vachon, Celine M
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Wang, Xianshu
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