Fine-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer.
Shi J., Zhang Y., Zheng W., Michailidou K., Ghoussaini M., Bolla MK., Wang Q., Dennis J., Lush M., Milne RL., Shu X-O., Beesley J., Kar S., Andrulis IL., Anton-Culver H., Arndt V., Beckmann MW., Zhao Z., Guo X., Benitez J., Beeghly-Fadiel A., Blot W., Bogdanova NV., Bojesen SE., Brauch H., Brenner H., Brinton L., Broeks A., Brüning T., Burwinkel B., Cai H., Canisius S., Chang-Claude J., Choi J-Y., Couch FJ., Cox A., Cross SS., Czene K., Darabi H., Devilee P., Droit A., Dork T., Fasching PA., Fletcher O., Flyger H., Fostira F., Gaborieau V., García-Closas M., Giles GG., Mervi Grip None., Guenel P., Haiman CA., Hamann U., Hartman M., Miao H., Hollestelle A., Hopper JL., Hsiung C-N., kConFab Investigators None., Ito H., Jakubowska A., Johnson N., Torres D., Kabisch M., Kang D., Khan S., Knight JA., Kosma V-M., Lambrechts D., Li J., Lindblom A., Lophatananon A., Lubinski J., Mannermaa A., Manoukian S., Le Marchand L., Margolin S., Marme F., Matsuo K., McLean C., Meindl A., Muir K., Neuhausen SL., Nevanlinna H., Nord S., Børresen-Dale A-L., Olson JE., Orr N., van den Ouweland AMW., Peterlongo P., Putti TC., Rudolph A., Sangrajrang S., Sawyer EJ., Schmidt MK., Schmutzler RK., Shen C-Y., Hou M-F., Shrubsole MJ., Southey MC., Swerdlow A., Teo SH., Thienpont B., Toland AE., Tollenaar RAEM., Tomlinson I., Truong T., Tseng C-C., Wen W., Winqvist R., Wu AH., Yip CH., Zamora PM., Zheng Y., Floris G., Cheng C-Y., Hooning MJ., Martens JWM., Seynaeve C., Kristensen VN., Hall P., Pharoah PDP., Simard J., Chenevix-Trench G., Dunning AM., Antoniou AC., Easton DF., Cai Q., Long J.
Previous genome-wide association studies among women of European ancestry identified two independent breast cancer susceptibility loci represented by single nucleotide polymorphisms (SNPs) rs13281615 and rs11780156 at 8q24. A fine-mapping study across 2.06 Mb (chr8:127,561,724-129,624,067, hg19) in 55,540 breast cancer cases and 51,168 controls within the Breast Cancer Association Consortium was conducted. Three additional independent association signals in women of European ancestry, represented by rs35961416 (OR = 0.95, 95% CI = 0.93-0.97, conditional p = 5.8 × 10(-6) ), rs7815245 (OR = 0.94, 95% CI = 0.91-0.96, conditional p = 1.1 × 10(-6) ) and rs2033101 (OR = 1.05, 95% CI = 1.02-1.07, conditional p = 1.1 × 10(-4) ) were found. Integrative analysis using functional genomic data from the Roadmap Epigenomics, the Encyclopedia of DNA Elements project, the Cancer Genome Atlas and other public resources implied that SNPs rs7815245 in Signal 3, and rs1121948 in Signal 5 (in linkage disequilibrium with rs11780156, r(2) = 0.77), were putatively functional variants for two of the five independent association signals. The results highlighted multiple 8q24 variants associated with breast cancer susceptibility in women of European ancestry.