Artigo Acesso aberto Revisado por pares

Fine-Scale Mapping of the 4q24 Locus Identifies Two Independent Loci Associated with Breast Cancer Risk

2015; American Association for Cancer Research; Volume: 24; Issue: 11 Linguagem: Inglês

10.1158/1055-9965.epi-15-0363

ISSN

1538-7755

Autores

Xingyi Guo, Jirong Long, Chenjie Zeng, Kyriaki Michailidou, Maya Ghoussaini, Manjeet K. Bolla, Sophia Wang, Roger L. Milne, Xiao-Ou Shu, Qiuyin Cai, Jonathan Beesley, Siddhartha Kar, Irene L. Andrulis, Hoda Anton‐Culver, Volker Arndt, Matthias W. Beckmann, Alicia Beeghly‐Fadiel, Javier Benı́tez, William J. Blot, Natalia Bogdanova, Stig E. Bojesen, Hiltrud Brauch, Hermann Brenner, Louise A. Brinton, Annegien Broeks, Thomas Brüning, Barbara Burwinkel, Hui Cai, Sander Canisius, Jenny Chang‐Claude, Ji‐Yeob Choi, Fergus J. Couch, Angela Cox, Simon S. Cross, Kamila Czene, Hatef Darabi, Peter Devilee, Arnaud Droit, Thilo Dörk, Peter A. Fasching, Olivia Fletcher, Henrik Flyger, Florentia Fostira, Valérie Gaborieau, Montserrat García‐Closas, Graham G. Giles, Mervi Grip, Pascal Guénel, Christopher A. Haiman, Ute Hamann, Mikael Hartman, Antoinette Hollestelle, John L. Hopper, Chia-Ni Hsiung, Hidemi Ito, Anna Jakubowska, Nichola Johnson, Maria Kabisch, Daehee Kang, Sofia Khan, Julia A. Knight, Veli-Matti Kosma, Diether Lambrechts, Loı̈c Le Marchand, Jingmei Li, Annika Lindblom, Artitaya Lophatananon, Jan Lubiński, Graham J. Mann, Siranoush Manoukian, Sara Margolin, Frederik Marmé, Keitaro Matsuo, Catriona McLean, Alfons Meindl, Kenneth Muir, Susan L. Neuhausen, Heli Nevanlinna, Silje Nord, Janet E. Olson, Nick Orr, Paolo Peterlongo, Thomas Choudary Putti, Anja Rudolph, Suleeporn Sangrajrang, Elinor J. Sawyer, Marjanka K. Schmidt, Rita K. Schmutzler, Chen‐Yang Shen, Jiajun Shi, Martha J. Shrubsole, Melissa C. Southey, Anthony J. Swerdlow, Soo‐Hwang Teo, Bernard Thienpont, Amanda E. Toland, Robert A.E.M. Tollenaar, Ian Tomlinson, Thérèse Truong, Chiu-Chen Tseng, Ans van den Ouweland, Wanqing Wen, Robert Winqvist, Anna H. Wu, Cheng Har Yip, M. Pilar Zamora, Ying Zheng, Per Hall, Paul D.P. Pharoah, Jacques Simard, Georgia Chenevix‐Trench, Alison M. Dunning, Douglas F. Easton, Wei Zheng,

Tópico(s)

Genetic factors in colorectal cancer

Resumo

Abstract Background: A recent association study identified a common variant (rs9790517) at 4q24 to be associated with breast cancer risk. Independent association signals and potential functional variants in this locus have not been explored. Methods: We conducted a fine-mapping analysis in 55,540 breast cancer cases and 51,168 controls from the Breast Cancer Association Consortium. Results: Conditional analyses identified two independent association signals among women of European ancestry, represented by rs9790517 [conditional P = 2.51 × 10−4; OR, 1.04; 95% confidence interval (CI), 1.02–1.07] and rs77928427 (P = 1.86 × 10−4; OR, 1.04; 95% CI, 1.02–1.07). Functional annotation using data from the Encyclopedia of DNA Elements (ENCODE) project revealed two putative functional variants, rs62331150 and rs73838678 in linkage disequilibrium (LD) with rs9790517 (r2 ≥ 0.90) residing in the active promoter or enhancer, respectively, of the nearest gene, TET2. Both variants are located in DNase I hypersensitivity and transcription factor–binding sites. Using data from both The Cancer Genome Atlas (TCGA) and Molecular Taxonomy of Breast Cancer International Consortium (METABRIC), we showed that rs62331150 was associated with level of expression of TET2 in breast normal and tumor tissue. Conclusion: Our study identified two independent association signals at 4q24 in relation to breast cancer risk and suggested that observed association in this locus may be mediated through the regulation of TET2. Impact: Fine-mapping study with large sample size warranted for identification of independent loci for breast cancer risk. Cancer Epidemiol Biomarkers Prev; 24(11); 1680–91. ©2015 AACR.

Referência(s)