11q13 is a susceptibility locus for hormone receptor positive breast cancer

A recent two‐stage genome‐wide association study (GWAS) identified five novel breast cancer susceptibility loci on chromosomes 9, 10, and 11. To provide more reliable estimates of the relative risk associated with these loci and investigate possible heterogeneity by subtype of breast cancer, we genotyped the variants rs2380205, rs1011970, rs704010, rs614367, and rs10995190 in 39 studies from the Breast Cancer Association Consortium (BCAC), involving 49,608 cases and 48,772 controls of predominantly European ancestry. Four of the variants showed clear evidence of association (P ≤ 3 × 10−9) and weak evidence was observed for rs2380205 (P = 0.06). The strongest evidence was obtained for rs614367, located on 11q13 (per‐allele odds ratio 1.21, P = 4 × 10−39). The association for rs614367 was specific to estrogen receptor (ER)‐positive disease and strongest for ER plus progesterone receptor (PR)‐positive breast cancer, whereas the associations for the other three loci did not differ by tumor subtype. Hum Mutat 33:1123–1132, 2012. © 2012 Wiley Periodicals, Inc.

Patrick Neven | Michael Jones | Michael Bremer | Julian Peto | Thomas Brüning | Kamila Czene | Ute Hamann | Peter Devilee | Gord Glendon | Alfons Meindl | Katarzyna Durda | Thilo Dörk | Barbara Burwinkel | Katri Pylkäs | Mervi Grip | Arto Mannermaa | Paolo Peterlongo | Annegien Broeks | Hermann Brenner | Per Hall | Børge G. Nordestgaard | Heli Nevanlinna | Angela Cox | Robert Winqvist | Annika Lindblom | Anthony Swerdlow | Vessela Kristensen | Pascal Guénel | Kristiina Aittomäki | Carl Blomqvist | Vesa Kataja | Christa Stegmaier | Volker Arndt | Argyrios Ziogas | Carmel Apicella | Jolanta Lissowska | Ian Tomlinson | Nicola Miller | Andreas Schneeweiss | Laura Baglietto | Olivia Fletcher | Nichola Johnson | Sten Cornelissen | Stefan Nickels | Paolo Radice | Anna Jakubowska | Jan Lubinski | Hiltrud Brauch | Elinor Sawyer | Diether Lambrechts | Alan Ashworth | Sarah Schott | Christof Sohn | Peter Hillemanns | Gianluca Severi | Javier Benítez | Daehee Kang | Puttisak Puttawibul | Rebecca Hein | Katarzyna Jaworska | Jianjun Liu | Artitaya Lophatananon | Therese Truong | S. Cross | R. Schulz-Wendtland | M. Beckmann | P. Fasching | A. Ashworth | A. Børresen-Dale | D. Noh | K. Czene | P. Hall | J. Olson | F. Couch | A. Schneeweiss | H. Brenner | J. Chang-Claude | S. Chanock | M. García-Closas | J. Benítez | P. Neven | G. Giles | G. Severi | J. Hopper | E. John | T. Dörk | M. Southey | A. Lophatananon | A. Cox | D. Easton | Chen-Yang Shen | A. Broeks | P. Pharoah | D. Lambrechts | J. Peto | E. Khusnutdinova | N. Orr | H. Brauch | M. Sherman | V. Kristensen | C. Sohn | P. Hillemanns | A. Ziogas | H. Anton-Culver | P. Guénel | A. Dunning | Pei-Ei Wu | O. Fletcher | N. Johnson | G. Chenevix-Trench | S. Bojesen | B. Nordestgaard | J. Lissowska | H. Nevanlinna | D. Kang | K. Yoo | Jianjun Liu | N. Bogdanova | P. Schürmann | R. Tollenaar | P. Devilee | I. Brock | R. Milne | C. Justenhoven | U. Hamann | Y. Ko | J. Beesley | Xiaoqing Chen | A. Mannermaa | V. Kosma | V. Kataja | J. Hartikainen | N. Miller | M. Kerin | K. Muir | A. Lindblom | M. Schmidt | I. D. S. Silva | T. Muranen | K. Aittomäki | C. Blomqvist | R. Hein | A. Meindl | R. Schmutzler | Xianshu Wang | R. Paridaens | S. Nickels | D. Flesch‐Janys | T. Truong | F. Menegaux | B. Burwinkel | M. P. Zamora | J. I. Pérez | E. Sawyer | I. Tomlinson | I. Andrulis | G. Glendon | A. Mulligan | S. Margolin | M. Hooning | G. Dite | C. Apicella | L. Baglietto | A. Ekici | H. Müller | V. Arndt | C. Stegmaier | A. Swerdlow | Michael Jones | R. Winqvist | K. Pylkäs | A. Jukkola-Vuorinen | M. Grip | T. Brüning | P. Radice | P. Peterlongo | S. Manoukian | C. Seynaeve | A. Jakubowska | J. Lubiński | Katarzyna Jaworska | K. Durda | N. Antonenkova | H. Wildiers | M. Bermisheva | M. Bremer | U. Eilber | S. Wang-gohrke | C. Bartram | M. Hou | Z. Fredericksen | M. Humphreys | J. Karstens | S. Cornelissen | G. Elliott | Jyh‐cherng Yu | A. Miron | L. Bernard | S. Schott | Kconfab Investigators | E. Cordina-Duverger | Darya Prokofieva | Sara Margolin | kConFab Investigators | Nicholas Orr | Siranoush Manoukian | Robert Paridaens | Hans Wildiers | F. Marmé | Xiaoqing Chen | Jenny Chang‐Claude | Douglas F. Easton | Jonathan Beesley | Elza Khusnutdinova | Christina Justenhoven | Heiko Müller | G. G. Alnæs | Stephen J. Chanock | Irene L. Andrulis | Marina Bermisheva | Anna Marie Mulligan | Darya Prokofieva | Peter Schürmann | Melissa Southey | Graham Giles | Veli‐Matti Kosma | Montserrat García‐Closas | Loris Bernard | Alexander Miron | Zachary Fredericksen | Xianshu Wang | Mark E. Sherman | Florence Menegaux | Teresa Selander | John L. Hopper | Michael Kerin | Graeme Elliott | Esther M. John | Suthee Rattanamongkongul | Matthias W. Beckmann | Arif B. Ekici | Anne‐Lise Børresen‐Dale | Janet E. Olson | Peter A. Fasching | Fergus J. Couch | P. Puttawibul | Hoda Anton‐Culver | Jean Wang | Simon S. Cross | Alison M. Dunning | Roger L. Milne | Stig E. Bojesen | Jaana M. Hartikainen | Yon‐Dschun Ko | Emilie Cordina‐Duverger | Melissa C. Southey | Dieter Flesch‐Janys | Georgia Chenevix‐Trench | Marjanka K. Schmidt | Charlotte Lanng | Manjeet K. Humphreys | Gillian S. Dite | Richard van Hien | M. Pilar Zamora | José Ignacio Arias Pérez | Ursel Eilber | Shan Wang‐Gohrke | Arja Jukkola‐Vuorinen | Chen‐Yang Shen | Jyh‐Cherng Yu | Pei‐Ei Wu | Ming‐Feng Hou | Kenneth R. Muir | Federik Marmé | Betul T. Yesilyurt | Claus R. Bartram | Rita K. Schmutzler | Ian W. Brock | Ruediger Schulz‐Wendtland | Isabel dos Santos Silva | Taru A. Muranen | Natalia V. Bogdanova | Natalia N. Antonenkova | Yuri I. Rogov | Johann H. Karstens | Shamil Gancev | Grethe Grenaker Alnæs | Robert A.E.M. Tollenaar | Caroline M. Seynaeve | Maartje J. Hooning | Keun‐Young Yoo | Dong‐Young Noh | Paul D.P. Pharoah | C. Lanng | B. T. Yesilyurt | Jean Wang | Suthee Rattanamongkongul | R. van Hien | T. Selander | Y. Rogov | S. Gancev

[1]  W. Willett,et al.  A genome-wide association study identifies alleles in FGFR 2 associated with risk of sporadic postmenopausal breast cancer , 2012 .

[2]  Patrick Neven,et al.  Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium. , 2011, Human molecular genetics.

[3]  D. Yee,et al.  Killing the second messenger: targeting loss of cell cycle control in endocrine-resistant breast cancer. , 2011, Endocrine-related cancer.

[4]  O. Gaye,et al.  Breast cancer risk by occupation and industry: analysis of the CECILE study, a population-based case-control study in France. , 2011, American journal of industrial medicine.

[5]  Victoria L. Cafourek,et al.  Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the Breast Cancer Association Consortium studies. , 2011, Journal of the National Cancer Institute.

[6]  Talin Haritunians,et al.  Variants in ZNF365 isoform D are associated with Crohn's disease , 2011, Gut.

[7]  Nathaniel D. Heintzman,et al.  9p21 DNA variants associated with Coronary Artery Disease impair IFNγ signaling response , 2011, Nature.

[8]  Peter Kraft,et al.  Common variants in ZNF365 are associated with both mammographic density and breast cancer risk , 2011, Nature Genetics.

[9]  Christiana Kartsonaki,et al.  A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general population , 2010, Nature Genetics.

[10]  Deborah Hughes,et al.  Genome-wide association study identifies five new breast cancer susceptibility loci , 2010, Nature Genetics.

[11]  J. Diehl,et al.  Nuclear cyclin D1: An oncogenic driver in human cancer , 2009, Journal of cellular physiology.

[12]  Melissa Bondy,et al.  Genome-wide association study identifies five susceptibility loci for glioma , 2009, Nature Genetics.

[13]  M. Beckmann,et al.  Risk of estrogen receptor-positive and -negative breast cancer and single-nucleotide polymorphism 2q35-rs13387042. , 2009, Journal of the National Cancer Institute.

[14]  Alexander R. Pico,et al.  Variants in the CDKN2B and RTEL1 regions are associated with high grade glioma susceptibility , 2009, Nature Genetics.

[15]  T. Spector,et al.  Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi , 2009, Nature Genetics.

[16]  M. Thun,et al.  Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2 , 2009, Nature Genetics.

[17]  W. Willett,et al.  A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1) , 2009, Nature Genetics.

[18]  A. Jakubowska,et al.  Do BRCA1 modifiers also affect the risk of breast cancer in non-carriers? , 2009, European journal of cancer.

[19]  Giu-Cheng Hsu,et al.  Genetic variants of BLM interact with RAD51 to increase breast cancer susceptibility. , 2009, Carcinogenesis.

[20]  N. Miller,et al.  The TGFBR1*6A/9A polymorphism is not associated with differential risk of breast cancer , 2009, Breast Cancer Research and Treatment.

[21]  P. Radice,et al.  SNPs in ultraconserved elements and familial breast cancer risk. , 2009, Carcinogenesis.

[22]  T. Dörk,et al.  A nonsense mutation (E1978X) in the ATM gene is associated with breast cancer , 2009, Breast Cancer Research and Treatment.

[23]  N. Miller,et al.  Low penetrance breast cancer predisposition SNPs are site specific , 2009, Breast Cancer Research and Treatment.

[24]  J. Kładny,et al.  Genetic contribution to all cancers: the first demonstration using the model of breast cancers from Poland stratified by age at diagnosis and tumour pathology , 2009, Breast Cancer Research and Treatment.

[25]  P. Bugert,et al.  SNPs in ultraconserved elements and familial breast cancer risk. , 2009, Carcinogenesis.

[26]  P. Radice,et al.  Evidences for association of the CASP8 -652 6N del promoter polymorphism with age at diagnosis in familial breast cancer cases , 2009, Breast Cancer Research and Treatment.

[27]  J. Chang-Claude,et al.  Risk of different histological types of postmenopausal breast cancer by type and regimen of menopausal hormone therapy , 2008, International journal of cancer.

[28]  Elmar Bucher,et al.  Genome‐wide analysis identifies 16q deletion associated with survival, molecular subtypes, mRNA expression, and germline haplotypes in breast cancer patients , 2008, Genes, chromosomes & cancer.

[29]  H. Brenner,et al.  Epigenotyping in Peripheral Blood Cell DNA and Breast Cancer Risk: A Proof of Principle Study , 2008, PloS one.

[30]  A. Sigurdsson,et al.  Common variants on chromosome 5p12 confer susceptibility to estrogen receptor–positive breast cancer , 2008, Nature Genetics.

[31]  O. Bernard,et al.  Fusion of ZMIZ1 to ABL1 in a B-cell acute lymphoblastic leukaemia with a t(9;10)(q34;q22.3) translocation , 2008, Leukemia.

[32]  B. van Calster,et al.  In early-stage breast cancer, the estrogen receptor interacts with correlation between human epidermal growth factor receptor 2 status and age at diagnosis, tumor grade, and lymph node involvement. , 2008, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[33]  M. Bani,et al.  Single nucleotide polymorphism D1853N of the ATM gene may alter the risk for breast cancer , 2008, Journal of Cancer Research and Clinical Oncology.

[34]  E. van Limbergen,et al.  Does estrogen receptor negative/progesterone receptor positive breast carcinoma exist? , 2008, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[35]  M. Bani,et al.  Single nucleotide polymorphisms of the aromatase gene (CYP19A1), HER2/neu status, and prognosis in breast cancer patients , 2008, Breast Cancer Research and Treatment.

[36]  T. Illig,et al.  The CYP1B1_1358_GG genotype is associated with estrogen receptor-negative breast cancer , 2008, Breast Cancer Research and Treatment.

[37]  W. Han,et al.  CASP8 polymorphisms, estrogen and progesterone receptor status, and breast cancer risk , 2008, Breast Cancer Research and Treatment.

[38]  A. Whittemore,et al.  Association Between Single-Nucleotide Polymorphisms in Hormone Metabolism and DNA Repair Genes and Epithelial Ovarian Cancer: Results from Two Australian Studies and an Additional Validation Set , 2007, Cancer Epidemiology Biomarkers & Prevention.

[39]  J. Klijn,et al.  Clinical correlates of low-risk variants in FGFR2, TNRC9, MAP3K1, LSP1 and 8q24 in a Dutch cohort of incident breast cancer cases , 2007, Breast Cancer Research.

[40]  Chen-Yang Shen,et al.  Breast Cancer Risk Is Associated with the Genes Encoding the DNA Double-Strand Break Repair Mre11/Rad50/Nbs1 Complex , 2007, Cancer Epidemiology Biomarkers & Prevention.

[41]  D. Gudbjartsson,et al.  Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor–positive breast cancer , 2007, Nature Genetics.

[42]  Lester L. Peters,et al.  Genome-wide association study identifies novel breast cancer susceptibility loci , 2007, Nature.

[43]  M. McCarthy,et al.  Replication of Genome-Wide Association Signals in UK Samples Reveals Risk Loci for Type 2 Diabetes , 2007, Science.

[44]  W. Willett,et al.  A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer , 2007, Nature Genetics.

[45]  Douglas B. Evans,et al.  Aurora-A and p16 Polymorphisms Contribute to an Earlier Age at Diagnosis of Pancreatic Cancer in Caucasians , 2007, Clinical Cancer Research.

[46]  Katri Pylkäs,et al.  A recurrent mutation in PALB2 in Finnish cancer families , 2007, Nature.

[47]  R. Vierkant,et al.  A Comprehensive Examination of CYP19 Variation and Breast Density , 2007, Cancer Epidemiology Biomarkers & Prevention.

[48]  S. Bojesen,et al.  Increased risk of breast cancer associated with CHEK2*1100delC. , 2006, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[49]  J. Peterse,et al.  Breast cancer survival and tumor characteristics in premenopausal women carrying the CHEK2*1100delC germline mutation. , 2006, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[50]  Chen-Yang Shen,et al.  Breast Cancer Risk Is Associated with the Genes Encoding the DNA Double-Strand Break Repair Mre11/Rad50/Nbs1 Complex , 2007, Cancer Epidemiology, Biomarkers and Prevention.

[51]  Paul D.P. Pharoah,et al.  Commonly studied single-nucleotide polymorphisms and breast cancer: results from the Breast Cancer Association Consortium. , 2007, Journal of the National Cancer Institute.

[52]  Genica,et al.  Commonly studied single-nucleotide polymorphisms and breast cancer: Results from the Breast Cancer Association Consortium , 2006 .

[53]  Joaquín Dopazo,et al.  ERCC4 associated with breast cancer risk: a two-stage case-control study using high-throughput genotyping. , 2006, Cancer research.

[54]  A. Ashworth,et al.  Inconsistent association between the STK15 F31I genetic polymorphism and breast cancer risk. , 2006, Journal of the National Cancer Institute.

[55]  A. Mannermaa,et al.  Refinement of the 22q12-q13 Breast Cancer–Associated Region: Evidence of TMPRSS6 as a Candidate Gene in an Eastern Finnish Population , 2006, Clinical Cancer Research.

[56]  P. Bugert,et al.  Association of the CASP10 V410I variant with reduced familial breast cancer risk and interaction with the CASP8 D302H variant. , 2006, Carcinogenesis.

[57]  S. Chanock,et al.  Polymorphisms in DNA double-strand break repair genes and risk of breast cancer: two population-based studies in USA and Poland, and meta-analyses , 2006, Human Genetics.

[58]  John L Hopper,et al.  Analysis of cancer risk and BRCA1 and BRCA2 mutation prevalence in the kConFab familial breast cancer resource , 2006, Breast Cancer Research.

[59]  W. Han,et al.  Genetic Polymorphisms of Ataxia Telangiectasia Mutated and Breast Cancer Risk , 2005, Cancer Epidemiology Biomarkers & Prevention.

[60]  Päivi Heikkilä,et al.  Correlation of CHEK2 protein expression and c.1100delC mutation status with tumor characteristics among unselected breast cancer patients , 2005, International journal of cancer.

[61]  D. Easton,et al.  An autosome-wide scan for linkage disequilibrium-based association in sporadic breast cancer cases in eastern Finland: three candidate regions found. , 2005, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

[62]  H. Brauch,et al.  Factors Modifying the Association Between Hormone-Replacement Therapy and Breast Cancer Risk , 2005, European Journal of Epidemiology.

[63]  C. Larsson,et al.  Hereditary breast cancer in sweden: a predominance of maternally inherited cases , 2005, Breast Cancer Research and Treatment.

[64]  B. Ponder,et al.  Association of a common variant of the CASP8 gene with reduced risk of breast cancer. , 2004, Journal of the National Cancer Institute.

[65]  M. Schutte,et al.  Tumour characteristics and prognosis of breast cancer patients carrying the germline CHEK2*1100delC variant , 2004, Journal of Medical Genetics.

[66]  A. Lindblom,et al.  BRCA1 mutations in a population-based study of breast cancer in Stockholm County. , 2004, Genetic testing.

[67]  Norman Boyd,et al.  The Breast Cancer Family Registry: an infrastructure for cooperative multinational, interdisciplinary and translational studies of the genetic epidemiology of breast cancer , 2004, Breast Cancer Research.

[68]  J. Chang-Claude,et al.  Breastfeeding and breast cancer risk by age 50 among women in Germany , 2000, Cancer Causes & Control.

[69]  John L Hopper,et al.  Familial risks, early-onset breast cancer, and BRCA1 and BRCA2 germline mutations. , 2003, Journal of the National Cancer Institute.

[70]  T. Stephenson,et al.  A potential role for the XRCC2 R188H polymorphic site in DNA-damage repair and breast cancer. , 2002, Human molecular genetics.

[71]  T. Stephenson,et al.  A potential role for the XRCC 2 R 188 H polymorphic site in DNA-damage repair and breast cancer , 2002 .

[72]  D. English,et al.  The Melbourne Collaborative Cohort Study. , 2002, IARC scientific publications.

[73]  T. Dörk,et al.  Spectrum of ATM gene mutations in a hospital-based series of unselected breast cancer patients. , 2001, Cancer research.

[74]  K Holli,et al.  Population-based study of BRCA1 and BRCA2 mutations in 1035 unselected Finnish breast cancer patients. , 2000, Journal of the National Cancer Institute.

[75]  A. Ziogas,et al.  Characteristics of BRCA1 mutations in a population-based case series of breast and ovarian cancer. , 2000, European journal of cancer.

[76]  D. Seminara,et al.  Cancer risk estimates for family members of a population-based family registry for breast and ovarian cancer. , 2000, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

[77]  J. Bartek,et al.  Amplification of chromosome band 11q13 and a role for cyclin D1 in human breast cancer. , 1995, Cancer letters.