Common Genetic Variation in Circadian Rhythm Genes and Risk of Epithelial Ovarian Cancer (EOC)
Heather S.L. Jim1, Hui-Yi Lin2 , Jonathan P. Tyrer3, Kate Lawrenson4, Joe Dennis3, Ganna Chornokur5, Zhihua Chen2, Ann Y. Chen2, Jennifer Permuth-Wey5, Katja KH. Aben6,7, Hoda Anton-Culver8, Natalia Antonenkova9, Fiona Bruinsma10, Elisa V. Bandera11, Yukie T. Bean12,13, Matthias W. Beckmann14, Maria Bisogna15, Line Bjorge16,17, Natalia Bogdanova18, Louise A. Brinton19, Angela Brooks-Wilson20,21, Clareann H. Bunker22, Ralf Butzow23,24, Ian G. Campbell25,26,27, Karen Carty28,29, Jenny Chang-Claude30, Linda S. Cook31, Daniel W. Cramer32, Julie M. Cunningham33, Cezary Cybulski34, Agnieszka Dansonka-Mieszkowska35, Andreas du Bois36,37, Evelyn Despierre38, Weiva Sieh39, Jennifer A. Doherty40,41, Thilo Dörk18, Matthias Dürst42, Douglas F. Easton43,44, Diana M. Eccles45, Robert P. Edwards46, Arif B. Ekici47, Peter A. Fasching14,48, Brooke L. Fridley49, Yu-Tang Gao50, Aleksandra Gentry-Maharaj51, Graham G. Giles10,52, Rosalind Glasspool29, Marc T. Goodman53,54, Jacek Gronwald34, Philipp Harter36,37, Hanis N. Hasmad55, Alexander Hein14, Florian Heitz36,37, Michelle A.T. Hildebrandt56, Peter Hillemanns18, Claus K. Hogdall57, Estrid Hogdall58,59, Satoyo Hosono60, Edwin S. Iversen61, Anna Jakubowska34, Allan Jensen58, Bu-Tian Ji19, Beth Y. Karlan62, Melissa Kellar12,13, Lambertus A. Kiemeney6, Camilla Krakstad16,17, Susanne K. Kjaer57,58, Jolanta Kupryjanczyk35, Robert A. Vierkant63, Diether Lambrechts64,65, Sandrina Lambrechts38, Nhu D. Le66, Alice W. Lee4, Shashi Lele67, Arto Leminen23, Jenny Lester62, Douglas A. Levine15, Dong Liang68, Boon Kiong Lim69, Jolanta Lissowska70, Karen Lu71, Jan Lubinski34, Lene Lundvall57, Leon F.A.G. Massuger72, Keitaro Matsuo60, Valerie McGuire73, John R. McLaughlin74, Ian McNeish29, Usha Menon51, Roger L. Milne10,52, Francesmary Modugno2,75,76, Lotte Thomsen77, Kirsten B. Moysich67, Roberta B. Ness78, Heli Nevanlinna23, Ursula Eilber30, Kunle Odunsi79, Sara H. Olson80, Irene Orlow80, Sandra Orsulic62, Rachel Palmieri Weber81, James Paul29, Celeste L. Pearce2,82, Tanja Pejovic12,13, Liisa M. Pelttari23, Malcolm C. Pike4,80, Elizabeth M. Poole83, Eva Schernhammer83,84, Harvey A. Risch85, Barry Rosen86, Mary Anne Rossing41, Joseph H. Rothstein39, Anja Rudolph30, Ingo B. Runnebaum42, Iwona K. Rzepecka35, Helga B. Salvesen16,17, Ira Schwaab87, Xiao-Ou Shu88, Yurii B. Shvetsov89, Nadeem Siddiqui28, Honglin Song4, Melissa C. Southey26, Beata Spiewankiewicz90, Lara Sucheston-Campbell67, Soo-Hwang Teo55,91, Kathryn L. Terry32,84, Pamela J. Thompson53,54, Ingvild L. Tangen16,17, Shelley S. Tworoger83,84, Anne M. van Altena72, Ignace Vergote38, Christine S. Walsh62, Shan Wang-Gohrke30, Nicolas Wentzensen19, Alice S. Whittemore39, Kristine G. Wicklund41, Lynne R. Wilkens89, Anna H. Wu4, Xifeng Wu56, Yin-Ling Woo69, Hannah Yang19, Wei Zheng92, Argyrios Ziogas8, Ernest Amankwah5,93, Andrew Berchuck94, Georgia Chenevix-Trench on behalf of the AOCS management group95,96, Joellen M. Schildkraut97, Linda E. Kelemen98, Susan J. Ramus4, Alvaro N.A. Monteiro5, Ellen L. Goode99, Steven A. Narod100, Simon A. Gayther4, Paul D. P. Pharoah3,101, Thomas A. Sellers5 and Catherine M. Phelan5*
1Department of Health Outcomes and Behavior, Moffitt Cancer Center, Tampa, FL, USA
2Department of Biostatistics and Bioinformatics, Moffitt Cancer Center, Tampa, FL, USA
3Department of Public Health and Primary Care, The Centre for Cancer Epidemiology, University of Cambridge, Strange ways Research Laboratory, Cambridge, UK
4Department of Preventive Medicine, Keck School of Medicine, University of Southern California Norris Comprehensive Cancer Center, Los Angeles, CA, USA
5Department of Cancer Epidemiology, Division of Population Sciences, Moffitt Cancer Center, Tampa, FL, USA
6Radboud University Medical Center, Radboud Institute for Health Sciences, Nijmegen, The Netherlands
7Netherlands Comprehensive Cancer Organization, Utrecht, The Netherlands
8Genetic Epidemiology Research Institute, UCI Center for Cancer Genetics Research and Prevention, School of Medicine, Department of Epidemiology, University of California Irvine, Irvine, CA, USA
9Byelorussian Institute for Oncology and Medical Radiology Aleksandrov N.N., Minsk, Belarus
10Cancer Epidemiology Centre, Cancer Council Victoria, Melbourne, Australia
11Cancer Prevention and Control, Rutgers Cancer Institute of New Jersey, New Brunswick, NJ, USA
12Department of Obstetrics & Gynecology, Oregon Health & Science University, Portland, OR, USA
13Knight Cancer Institute, Oregon Health & Science University, Portland, OR, USA
14Department of Gynecology and Obstetrics, University Hospital Erlangen, Friedrich-Alexander-University, Erlangen-Nuremberg Comprehensive Cancer Center, Erlangen EMN, Germany
15Department of Surgery, Gynecology Service, Memorial Sloan-Kettering Cancer Center, New York, NY, USA
16Department of Gynecology and Obstetrics, Haukeland University Hospital, Bergen, Norway
17Centre for Cancer Biomarkers, Department of Clinical Medicine, University of Bergen, Bergen, Norway
18Gynecology Research Unit, Hannover Medical School, Hannover, Germany
19Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, USA
20Canada's Michael Smith Genome Sciences Centre, BC Cancer Agency, Vancouver, BC, Canada
21Department of Biomedical Physiology and Kinesiology, Simon Fraser University, Burnaby, BC Canada
22Department of Epidemiology, University of Pittsburgh Graduate School of Public Health, Pittsburgh, PA, USA
23Department of Obstetrics and Gynecology, University of Helsinki and Helsinki University Central Hospital, Helsinki, HUS, Finland
24Department of Pathology, Helsinki University Central Hospital, Helsinki, HUS, Finland
25Cancer Genetics Laboratory, Research Division, Peter MacCallum Cancer Centre, St Andrews Place, East Melbourne, Australia.
26Department of Pathology, University of Melbourne, Parkville, Victoria, Australia
27Sir Peter MacCallum Department of Oncology, University of Melbourne, Parkville, Victoria, Australia
28Department of Gynaecological Oncology, Glasgow Royal Infirmary, Glasgow, G31 2ER, UK
29CRUK Clinical Trials Unit, The Beatson West of Scotland Cancer Centre, 1053 Great Western Road, Glasgow G12 0YN, UK
30German Cancer Research Center (DKFZ), Division of Cancer Epidemiology, Heidelberg, Germany
31Division of Epidemiology and Biostatistics, Department of Internal Medicine, University of New Mexico, Albuquerque, NM, USA
32Obstetrics and Gynecology Center, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA
33Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA
34International Hereditary Cancer Center, Department of Genetics and Pathology, Pomeranian Medical University, Szczecin, Poland
35Department of Pathology, The Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, Warsaw, Poland
36Department of Gynaecology and Gynaecologic Oncology, Kliniken Essen-Mitte/ Evang. Huyssens-Stiftung/ Knappschaft GmbH, Essen, Germany
37Department of Gynaecology and Gynaecologic Oncology, Dr. Horst Schmidt Kliniken Wiesbaden, Wiesbaden, Germany
38Division of Gynecologic Oncology; Leuven Cancer Institute, University Hospitals Leuven, KU Leuven, Leuven, Belgium
39Department of Health Research and Policy- Epidemiology, Stanford University School of Medicine, Stanford, CA, USA
40Department of Epidemiology, Geisel School of Medicine, Dartmouth, Hanover, NH, USA
41Program in Epidemiology, Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, University of Washington, Seattle, WA, USA
42Department of Gynecology, Friedrich Schiller University, Jena, Germany
43Department of Oncology, Centre for Cancer Genetic Epidemiology, University of Cambridge, Cambridge, UK
44Department of Public Health and Primary Care, Centre for Cancer Genetic Epidemiology, University of Cambridge, Cambridge, UK
45Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, UK
46Department of Obstetrics Gynecology/RS, Division of Gynecological Oncology, Ovarian Cancer Center of Excellence, University of Pittsburgh, Pittsburgh, PA, USA
4747Institute of Human Genetics, University Hospital Erlangen, Friedrich-Alexander-University Erlangen-Nuremberg, Erlangen, Germany
48Department of Medicine, Division of Hematology and Oncology, University of California at Los Angeles, David Geffen School of Medicine, Los Angeles, CA, USA
49Department of Biostatistics, University of Kansas Medical Center, Kansas City, KS, USA
50Department of Epidemiology, Shanghai Cancer Institute, Shanghai, China
51Women's Cancer, UCL EGA Institute for Women's Health, London, UK
52Centre for Epidemiology and Biostatistics, School of Population and Global Health, The University of Melbourne, Melbourne, Australia
53Cancer Prevention and Control, Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA
54Department of Biomedical Sciences, Community and Population Health Research Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA
55Cancer Research Initiatives Foundation, Sime Darby Medical Center, Subang Jaya, Malaysia
56Department of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA
57Department of Gynaecology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
58Department of Virus, Lifestyle and Genes, Danish Cancer Society Research Center, Copenhagen, Denmark
59Department of Pathology, Molecular Unit, Herlev Hospital, University of Copenhagen, Copenhagen, Denmark
60Division of Epidemiology and Prevention, Aichi Cancer Center Research Institute, Nagoya, Aichi, Japan
61Department of Statistics, Duke University, Durham, NC, USA
62Women's Cancer Program at the Samuel Oschin Comprehensive, Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA
63Department of Health Science Research, Division of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, MN, USA
64Vesalius Research Center, VIB, University of Leuven, Leuven, Belgium
65Department of Oncology, Laboratory for Translational Genetics, University of Leuven, Belgium
66Cancer Control Research, BC Cancer Agency, Vancouver, BC, Canada
67Department of Cancer Prevention and Control, Roswell Park Cancer Institute, Buffalo, NY, USA
68College of Pharmacy and Health Sciences, Texas Southern University, Houston, TX, USA
69Department of Obstetrics and Gynaecology, University Malaya Medical Centre, University Malaya, Kuala Lumpur, Malaysia
70Department of Cancer Epidemiology and Prevention, M. Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, Warsaw, Poland
71Department of Gynecologic Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA
72Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, Nijmegen, The Netherlands.
73Department of Health Research and Policy - Epidemiology, Stanford University School of Medicine, Stanford, CA, USA
74Public Health Ontario, Toronto, ON, Canada
75Women's Cancer Research Program, Magee-Women's Research Institute and University of Pittsburgh Cancer Institute, Pittsburgh, PA, USA
76Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA
77Department of Pathology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
78The University of Texas School of Public Health, Houston, TX, USA
79Department of Gynecologic Oncology, Roswell Park Cancer Institute, Buffalo, NY
80Department of Epidemiology and Biostatistics, Memorial Sloan-Kettering Cancer Center, New York, NY, USA
81Department of Community and Family Medicine, Duke University Medical Center, Durham, NC, USA
82Department of Epidemiology, University of Michigan,1415 Washington Heights, Ann Arbor, Michigan, USA.
83Channing Division of Network Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA
84Department of Epidemiology, Harvard School of Public Health, Boston, MA, USA
85Department of Chronic Disease Epidemiology, Yale School of Public Health, New Haven, CT, USA
86Department of Gynecology-Oncology, Princess Margaret Hospital, and Department of Obstetrics and Gynecology, Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada
87Institut für Humangenetik, Wiesbaden, Germany
88Epidemiology Center and Vanderbilt, Ingram Cancer Center, Vanderbilt University School of Medicine, Nashville, TN, USA
89Cancer Epidemiology Program, University of Hawaii Cancer Center, Hawaii, USA
90Department of Gynecologic Oncology, Institute of Oncology, Warsaw, Poland
91University Malaya Medical Centre, University of Malaya, Kuala Lumpur, Maylaysia
92Vanderbilt Epidemiology Center, Vanderbilt University School of Medicine, Nashville, TN, USA
93Clinical and Translational Research Organization, All Children's Hospital Johns Hopkins Medicine, St Petersburg, FL
94Department of Obstetrics and Gynecology, Duke University Medical Center, Durham, NC, USA
95QIMR Berghofer Medical Research Institute, Brisbane, Australia
96Peter MacCallum Cancer Centre, East Melbourne, Australia
97Cancer Prevention, Detection & Control Research Program, Duke Cancer Institute, Durham, NC, USA
98Department of Public Health Sciences, Medical University of South Carolina, Charleston, SC, USA
99Department of Health Science Research, Division of Epidemiology, Mayo Clinic, Rochester, MN, USA
100Women's College Research Institute, University of Toronto, Toronto, Ontario, Canada
101The Centre for Cancer Genetic Epidemiology, Department of Oncology, University of Cambridge, Cambridge, UK
*Corresponding author: Catherine M. Phelan, Department of Cancer Epidemiology, Moffitt Cancer Center, 12902 Magnolia Drive, Tampa, FL 33612, USA, Tel: 813-745-4971, E-mail: email@example.com
J Genet Genome Res, JGGR-2-017, (Volume 2, Issue 2), Research Article; ISSN: 2378-3648
Received: July 14, 2015 | Accepted: September 12, 2015 | Published: September 15, 2015
Citation: Jim HSL, Hui-Yi L, Tyrer JP, Lawrenson K, Dennis J, et al. (2015) Common Genetic Variation in Circadian Rhythm Genes and Risk of Epithelial Ovarian Cancer (EOC). J Genet Genome Res 2:017. 10.23937/2378-3648/1410017
Copyright: © 2015 Jim HSL, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Disruption in circadian gene expression, whether due to genetic variation or environmental factors (e.g., light at night, shiftwork), is associated with increased incidence of breast, prostate, gastrointestinal and hematologic cancers and gliomas. Circadian genes are highly expressed in the ovaries where they regulate ovulation; circadian disruption is associated with several ovarian cancer risk factors (e.g., endometriosis). However, no studies have examined variation in germline circadian genes as predictors of ovarian cancer risk and invasiveness. The goal of the current study was to examine single nucleotide polymorphisms (SNPs) in circadian genes BMAL1, CRY2, CSNK1E, NPAS2, PER3, REV1 and TIMELESS and downstream transcription factors KLF10 and SENP3 as predictors of risk of epithelial ovarian cancer (EOC) and histopathologic subtypes. The study included a test set of 3,761 EOC cases and 2,722 controls and a validation set of 44,308 samples including 18,174 (10,316 serous) cases and 26,134 controls from 43 studies participating in the Ovarian Cancer Association Consortium (OCAC). Analysis of genotype data from 36 genotyped SNPs and 4600 imputed SNPs indicated that the most significant association was rs117104877 in BMAL1 (OR = 0.79, 95% CI = 0.68-0.90, p = 5.59 × 10-4]. Functional analysis revealed a significant down regulation of BMAL1 expression following cMYC overexpression and increasing transformation in ovarian surface epithelial (OSE) cells as well as alternative splicing of BMAL1 exons in ovarian and granulosa cells. These results suggest that variation in circadian genes, and specifically BMAL1, may be associated with risk of ovarian cancer, likely through disruption of hormonal pathways.
Almost every human cell contains an autonomous circadian clock that synchronizes gene transcription in a daily oscillation for many physiological processes allowing for adaptation to the 24 hour environmental day/night cycle. Circadian genes are known to regulate a variety of cellular processes including the cell cycle, apoptosis, and DNA damage repair . Disruption in circadian gene expression, whether due to genetic variants or environmental factors (e.g., light at night, shiftwork), is associated with increased incidence and invasiveness of a variety of human cancers [2-5] such that in 2007 the International Agency for Research on Cancer classified shiftwork that involves circadian disruption as "a probable carcinogen" in humans . Disruption of circadian rhythms is also associated with disturbances in menstrual function; female shift workers compared to non-shift workers are more likely to report menstrual irregularity and longer menstrual cycles . Moreover, a recent study found that working nightshifts (i.e., 12:00-4:00 AM) was associated with an increased risk of serious and mucinous, invasive and borderline ovarian tumors in women who were 50 years of age and older . Nevertheless, some studies have failed to find an association between shiftwork and cancer risk [9-11].
The molecular mechanism of the mammalian circadian rhythm is a transcriptional-translational-post-translational autoregulatory feedback loop . The core of the loop consists of CLOCK and BMAL1 proteins, that form a dimer which binds to the E-box region in promoters of period (PER1, PER2, PER3) and cryptochrome (CRY1, CRY2) genes. Following transcription and translation, PER and CRY proteins form a complex with casein kinase 1 epsilon (CSNK1E) and translocate into the nucleus. Here they bind to BMAL1/CLOCK complex and inhibit their own transcription, which completes the basic auto regulatory loop. PER and CRY proteins are then tagged for proteasomal degradation via phosphorylation by CSNK1E and casein kinase 1 delta (CSNK1D) and subsequently by ubiquitination. This cycle lasts approximately 24 h. The BMAL1/CLOCK heterodimer also up regulates the transcription of Rev-erbα and Rora. Their protein products interact with ROR elements (RORE) in the promoter of BMAL1 gene, upregulating (RORα) or downregulating (REV-ERBα) its transcription [12,13].
Circadian rhythm genes in the hypothalamic suprachiasmatic nucleus (SCN) and reproductive tissues control the timing and length of the ovulatory cycle and pregnancy by their influence on hormones . Estradiol, synthesized in the ovary in response to the stimulation by gonadotropins from the hypothalamic-pituitary-gonadal (HPG) axis, influences the expression of circadian rhythm genes, and in a complex loop-back mechanism the circadian rhythm proteins interfere with estradiol signaling . Overexpression of CLOCK transcription factors may play a role in the pathogenesis of endometriosis , which is a risk factor for some subtypes of ovarian cancer [17-19]. Infertility is observed in knockout BMAL1, PER1, and PER2 mice [20-22]. These data are consistent with human studies indicating that genetic variation in BMAL1 is associated with increased rates of miscarriage . Nulliparity is a well-established risk factor for ovarian cancer, although it is currently unclear whether this association is due to infertility or other biological factors (e.g., increased ovulation) [24-27].
Variation in circadian genes has been associated with cancer susceptibility and outcomes. CLOCK1, CRY1, CRY2, NPAS2, PER1, RORA and TIMELESS variants are associated with breast cancer risk [5,28-33], while polymorphisms in BMAL1, CLOCK1, CRY1, CRY2, CSNK1E, NPAS2, PER1, PER2, and PER3 are associated with prostate cancer risk [34-36]. CRY2 and NPAS2 variation is associated with risk of non-Hodgkin's lymphoma [37,38] while polymorphisms in CLOCK1 are associated with colorectal cancer susceptibility . PER1 and CLOCK1 variation is associated with glioma risk and outcome  and PER3 polymorphisms have been associated with hepatocellular carcinoma survival . Interestingly, variation in many of these genes is also associated with dysregulation of circadian behaviors, including sleep and activity patterns [42,43], although data are conflicting [44,45]. To date, however, there are no published studies on the association of variation in circadian genes with ovarian cancer risk and invasiveness.
The goal of the current study was to examine variants in seven key circadian rhythm genes (BMAL1, CRY2, CSNK1E, NPAS2, PER3, REV1, TIMELESS) and two transcription factors (KLF10 and SENP3) activated by circadian rhythm gene expression as risk factors for epithelial ovarian cancer, histopathologic subtype, and invasiveness. SNPs were evaluated in a two-stage design: a discovery stage using two genome-wide association studies (GWAS) and a replication stage with approximately 44,000 cases and controls from 43 studies that comprise the Ovarian Cancer Association Consortium (OCAC).
Materials and Methods
Sample and procedure
The discovery set included 3,761 EOC cases and 2,722 controls in two ovarian cancer GWAS in North America and the United Kingdom (UK). Details of these studies have been previously published . In brief, the North American study was comprised of four case-control studies genotyped using the Illumina 610-quad Beadchip Array™ (i.e., 1,814 cases and 1,867 controls) as well as a single case-control study genotyped on the Illumina 317K and 370K arrays (i.e., 133 cases and 142 controls). The UK study was comprised of four case-only studies genotyped on the Illumina 610-quad Beadchip Array™ and two common control sets genotyped on the Illumina 550K array (i.e., 1,814 cases and 713 controls). The North American and UK studies were analyzed separately and the results combined using fixed effects meta-analysis.
The replication sample consisted of 14,525 invasive EOC cases and 23,447 controls from 43 sites in the Ovarian Cancer Association Consortium (OCAC). An additional 1,747 participants with tumors of low malignant potential were also analyzed. The sample consisted of only participants with European ancestry due to small numbers belonging to other racial groups.
Gene and SNP selection
Seven essential circadian genes (BMAL1, CRY2, CSNK1E, NPAS2, PER3, REV1, TIMELESS) and two key transcription factor genes activated by circadian genes (KLF10, SENP3) were selected a priori for examination. On the Illumina 610quad, 241 tagSNPs in these genes were identified. The selection of SNPs for replication was informed by ranking of minimal p-values across four sets of results: 1) North American all histologies, 2) North American serous histology, 3) combined GWAS meta-analysis all histologies, and 4) combined GWAS meta-analysis serous histology. Of the 241 SNPs, 37 SNPs were significant in the GWAS discovery set.
Demographic and clinical characteristics of cases and controls were compared using t-tests for continuous variables and chi-square tests for categorical variables. Unconditional logistic regression, treating the number of minor alleles carried as an ordinal variable (i.e., log-additive model), was used to evaluate the association between each SNP and ovarian cancer risk. Per-allele log odds ratios (OR) and their 95% confidence intervals (CI) were estimated. Models were adjusted for study site and population substructure by including study-site indicators and the first five eigenvalues from principal components analysis. The number of principal components was based on the position of the inflexion of the principal components scree plot.
To maximize statistical power, the combined COGS dataset was used to perform SNP-specific analyses for all invasive EOC, the four main histological subtypes (serous, endometrioid, clear cell and mucinous), and tumors of low malignant potential (LMP). Odds ratios specific for each histological subtype were estimated by comparing cases of each subtype to all available controls as reference. Associations with a two-sided p value < 0.05 and a false discovery rate (FDR) q-value  < 0.10 were considered to be statistically significant.
These analyses were based on imputed genotypes from the four ovarian cancer GWAS studies (US GWAS, UK GWAS, COGS and Mayo clinic) with a total of 15,398 invasive EOC case subjects and 30,816 control subjects of white-European ancestry. Imputation of each dataset into the 1000 Genomes Project was performed using IMPUTE2 software . We used the 1000 Genomes Project v3 as the reference with pre-phasing of the data using SHAPEIT . SNP log-additive model meta-analysis was carried out for combining results across studies. Only imputed SNPs with r2 > 0.25 for each study were used in the analyses.
An in vitro model of early-stage ovarian cancer has been previously described . Briefly, Illumina HT12 gene expression microarrays were used to profile the transcriptome of 3D models of normal ovarian cells immortalized with TERT and overexpressing cMYC and a mutant KRAS or BRAF allele.
All invasive cancers combined and the four main histological subtypes serous (n = 8,369), endometrioid (n = 2,067), clear cell (n = 1,024) and mucinous (n = 943) were analyzed. Sample characteristics are described in table 1. As expected, significant differences were observed between cases and controls on ovarian cancer risk factors including age, family history of ovarian cancer, age at menarche, body mass index (BMI), history of oral contraceptive use, endometriosis, and number of full term births (p values < 0.05). The proportion of serous histological subtype (57.6%) was higher than the other subtypes (14.2% endometrioid, 7.1% clear cell, 6.5% for mucinous, and 14.6% other).
Table 1: Sample demographic and clinical characteristics (n= 37,972). View Table 1
A total of 36 SNPs demonstrated p values < 0.05 in the screening stage and passed quality control. Of these, two in SENP3 (i.e., rs11656383, rs3499590) were rare variants (i.e., MAFs < 0.01) and were dropped from further analyses. Of the remaining 34 SNPs, 14 were associated with risk of overall EOC, histopathological subtype, and/or invasiveness (Table 2). Seven remained significant after applying the criterion of FDR < 0 .10. Specifically, one SNP was associated with risk of all invasive EOC, rs2513928 in KLF10 (OR = 0.95, 95% CI = 0.92-0.98, p = 1.75 × 10-3). Four SNPs in KLF10 were associated with risk of serous EOC (rs2513928: OR = 0.94, 95% CI = 0.91-0.98, p = 2.42 × 10-3; rs2511703: OR = 1.05, 95% CI = 1.02-1.09, p = 6.54 × 10-3; rs3191333: OR = 1.05, 95% CI = 1.02-1.10, p = 6.72 × 10-3; rs2513927: OR = 1.05, 95% CI = 1.01-1.09, p = 1.18 × 10-2). As shown in figure 1, linkage disequilibrium (LD) between the four significant SNPs in KLF10 was low to moderate. Risk of endometrioid EOC was associated with SENP3 rs6608 (OR = 1.13, 95% CI = 1.04-1.23, p = 4.43 ×10-3), CSNK1E rs135750 (OR = 1.13, 95% CI = 1.03-1.23, p = 7.09 × 10-3), REV1 rs3792152 (OR = 0.92, 95% CI = 0.86-0.98, p = 9.61 × 10-3), and BMAL1 rs10732458 (OR = 1.32, 95% CI = 1.07-1.63, p = 9.64 × 10-3). No SNPs were significantly associated with EOC invasiveness nor were any SNPs significantly associated with risk of mucinous or clear cell EOC after applying the criterion of FDR < 0.10.
Figure 1: Linkage Disequilibrium (r2) among Single Nucleotide Polymorphisms in KLF10. View Figure 1
Table 2: Associations between Genotyped SNPs in Circadian Genes and EOC Incidence Overall, in Histological Subtypes, and Invasiveness. View Table 2
A total of 4600 imputed SNPs in the nine genes of interest (BMAL1, CRY2, CSNK1E, NPAS2, PER3, REV1, TIMELESS, KLF10, SENP3) were then examined for association with all invasive EOC. A total of 304 SNPs across all nine genes met criteria for statistical significance (p < 0.05). Top hits in each gene with good imputation quality [r2 > 0.8] are shown in table 3. Across all genes, the most significant imputed SNP was rs117104877 in BMAL1 (OR = 0.79, 95% CI = 0.68-0.90, p = 5.59 × 10-4).
Table 3: Associations between the Top Imputed SNP in Each Gene with Good Imputation Quality (r2 > 0.8) and EOC Incidence Overall. View Table 3
Evaluating the functional role of BMAL1 in ovarian cancer
The role of BMAL1 in ovarian cancer was examined using in silico analysis of existing biological datasets in ovarian normal and tumor tissues and an in vitro cell biology model of early stage ovarian cancer development. We evaluated gene expression in normal fallopian tubes (n = 8) compared to high-grade serous ovarian carcinomas (HGSOCs, n = 489) using data from The Cancer Genome Atlas (TCGA), but there was no evidence that BMAL1 was differentially regulated in EOCs as compared to normal tissue (Figure 2).
Figure 2: (A) BMAL1 is not differentially expressed in TCGA expression data for 8 normal fallopian tubes and 489 high-grade serous EOCs; however, in an early stage model of ovarian cancer, (B) BMAL1 is downregulated in partially transformed ovarian epithelial cells overexpressing cMYC. BMAL1 downregulation is cMYC dependent, and not enhanced by the expression of a mutant KRAS allele. (C) 6 SNPs at the BMAL1 locus coincide with marks of active regulatory elements (H3K27Ac and H3K4me1) or transcription factor binding sites (TF ChiPseq) (arrows). One SNP, rs2896635 coincides with a commonly used enhancer that is active in ovarian stromal tissue (dashed box), and which targets the BMAL1 gene. ENCODE data and data from . View Figure 2
BMAL1 expression was further investigated in an early stage transformation model of EOC based on overexpression of CMYC in the ovarian surface epithelium (OSE) . BMAL1 was significantly down regulated in this model, but down regulation was not enhanced by expression of a mutant KRAS allele (Figure 2b). Risk associated SNPs were located within intronic regions of BMAL1 (Figure 2c) and clustered around a commonly described enhancer, suggesting that risk SNPs may influence enhancer activity. Rs2896635 in particular coincides with an enhancer used in many cell types, including an enhancer that is active in ovarian stromal cells that targets the BMAL1 gene . This suggests that non-cell autonomous signaling pathways may be involved in risk at this locus.
Circadian genes appear to play an important role in regulating reproductive cycles, including ovulation, the length of the estrous cycle, and maintenance of pregnancy. The current study examined variation in nine key genes involved in circadian rhythm regulation or their transcription (BMAL1, CRY2, CSNK1E, KLF10, NPAS2, PER3, REV1, SENP3, TIMELESS) as predictors of epithelial ovarian cancer risk, histopathologic subtype, and invasiveness. We found that 14 of the 34 genotyped SNPs in the discovery set were associated with risk of overall EOC, histopathological subtype, and/or invasiveness at p < 0.05. Seven remained significant after applying the criterion of FDR < 0.10. Specifically, risk of overall and serous EOC was associated with variants in KLF10 while risk of endometrioid EOC was associated with variants in SENP3, CSNK1E, REV1, and BMAL1. Of 4600 imputed variants in the nine genes of interest, 304 were found to be associated with overall EOC risk at p < . 05. Significant variants were found in all nine genes with the most significant located in BMAL1. Additional functional analyses of BMAL1 indicated that it was down regulated as a consequence of overexpressing cMYC in the OSE, although differential regulation was not observed in HGSOCs compared to normal fallopian tube tissue. Taken together, these results suggest that circadian rhythm genes may play a role in the development of EOC, particularly the genes KLF10 and BMAL1.
While previous research has implicated circadian genes in the development of several types of human cancer, the current study is the first to our knowledge to examine relationships with risk of ovarian cancer. Findings regarding the Krüppel-like factor 10 (KLF10) gene are consistent with a sizable body of experimental data indicating that KLF10 acts to inhibit cellular proliferation and induce apoptosis in a variety of cell types via regulation of transforming growth factor beta (TGFβ) and in turn SMAD [52-58]. KLF10 is a circadian transcriptional regulator that links the molecular clock to energy metabolism . KLF10 displays robust BMAL1-dependent circadian expression; the KLF10 promoter recruits BMAL1 and is transactivated by the CLOCK/BMAL1 dimer through a conserved E-box response element. To our knowledge the role of KLF10 in human ovarian cancer has not been investigated, although estrogen is known to increase KLF10 gene transcription [60,61]. KLF10 expression is reduced in breast tumors relative to normal tissue and is inversely correlated with stage of disease [62,63]. The KLF10-TGFβ-SMAD pathway has been implicated in the development of several other human cancers including those of the prostate, pancreas, kidney, lymphoma, and brain [53,64-67].
Our findings regarding BMAL1 are interesting in light of data suggesting that this gene may regulate the p53 tumor suppressor pathway. Specifically, silencing of BMAL1 gene expression prevents cell cycle arrest upon p53 activation in human fibroblast cells  and mouse colon and fibroblast cells . These data are consistent with research suggesting that BMAL1 is transcriptionally silenced via hypermethylation in hematologic malignancies; reintroduction of BMAL1 causes growth inhibition, while BMAL1 depletion by RNA interference increases tumor growth . The BMAL1 protein also has been shown to bind to the promoter region of VEGF where it regulates transcription and promotes angiogenesis .
Evidence suggests that, controlling for stage, histological subtype, and grade, low BMAL1 and CRY1 expression together significantly predict lower overall survival in ovarian cancer patients . Previous research also suggests significantly lower BMAL1 and CRY1 expression in EOC cells compared to normal ovarian tissue . The current study demonstrated downregulation of BMAL1 when cMYC was overexpressed in an early stage ovarian cancer transformation model, resulting in increasing ovarian epithelial cell transformation. Nevertheless, we did not observe differential regulation of BMAL1 when comparing EOC cells to normal fallopian tube tissue. Our findings suggest that down regulation of BMAL1 may be an early event in ovarian carcinogenesis and that BMAL1 is a novel cMYC target. SNPs statistically significant in the current study lie within intronic sequences of the BMAL1 gene and mechanisms by which they impact BMAL1 expression have yet to be elucidated. Nevertheless, our data suggest that this risk locus may modulate ovarian cancer risk by altering the ovarian stromal microenvironment, for example by influencing the character of ovarian fibroblasts or granulosa cells, both of which express BMAL1. In conclusion, our results highlight the significance of circadian rhythm gene variation in EOC susceptibility and suggest an early role for the BMAL1 gene in EOC pathogenesis.
Individual acknowledgements by study
We thank all the individuals who took part in this study and all the researchers, clinicians and technical and administrative staff who have made possible the many studies contributing to this work. In particular, we thank: D. Bowtell, A. deFazio, D. Gertig, A. Green, P. Parsons, N. Hayward, P. Webb and D. Whiteman (AUS); G. Peuteman, T. Van Brussel and D. Smeets (BEL); the staff of the genotyping unit, S LaBoissiere and F Robidoux (Genome Quebec); U. Eilber and T. Koehler (GER); L. Gacucova (HMO); P. Schurmann, F. Kramer, W. Zheng, T. W. Park, Simon, K. Beer- Grondke and D. Schmidt (HJO); S. Windebank, C. Hilker and J. Vollenweider (MAY); the state cancer registries of AL, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, IL, IN, IA, KY, LA, ME, MD, MA, MI, NE, NH, NJ, NY, NC, ND, OH, OK, OR, PA, RI, SC, TN, TX, VA, WA, and WYL (NHS); L. Paddock, M. King, L. Rodriguez-Rodriguez, A. Samoila, and Y. Bensman (NJO); M. Sherman, A. Hutchinson,N. Szeszenia--? Dabrowska, B. Peplonska, W. Zatonski, A. Soni, P. Chao and M. Stagner (POL); C. Luccarini,P. Harrington the SEARCH team and ECRIC (SEA); I. Jacobs, M. Widschwendter, E. Wozniak, N. Balogun, A. Ryan and J. Ford (UKO); Carole Pye (UKR); A. Amin Al Olama, K. Michilaidou, K. Kuchenbaker (COGS).
The scientific development and funding for this project were funded by the following: NIH R01 CA-1491429 (Phelan PI); the US National Cancer Institute (R01-CA076016); the COGS project is funded through a European Commission's Seventh Framework Program grant (agreement number 223175 HEALTH F2 2009-223175); the Genetic Associations and Mechanisms in Oncology (GAME?ON): a NCI Cancer Post-GWAS Initiative (U19-CA148112); the Ovarian Cancer Association Consortium is supported by a grant from the Ovarian Cancer Research Fund thanks to donations by the family and friends of Kathryn Sladek Smith (PPD/RPCI.07).
K.L is supported by a K99/R00 grant from the National Cancer Institute (Grant number 1K99CA184415-01). G.C.-T. is supported by the National Health and Medical Research Council; B.K. is supported by the American Cancer Society Early Detection Professorship (SIOP-06-258-01-COUN) and the National Center for Advancing Translational Sciences (NCATS), Grant UL1TR000124.; L.E.K. is supported by a Canadian Institute of Health Research New Investigator Award (MSH-87734). AWL is supported by NIEHS T32 training grant (T32ES013678).
Funding of included studies
Funding of the constituent studies was provided by the California Cancer Research Program (00-01389V-20170, N01-CN25403, 2II0200); the Canadian Institutes of Health Research (MOP-86727); Cancer Australia; Cancer Council Victoria; Cancer Council Queensland; Cancer Council New South Wales; Cancer Council South Australia; Cancer Council Tasmania; Cancer Foundation of Western Australia; the Cancer Institute of New Jersey; Cancer Research UK (C490/A6187, C490/A10119, C490/A10124); the Danish Cancer Society (94-222-52); the ELAN Program of the University of Erlangen-Nuremberg; the Eve Appeal; the Helsinki University Central Hospital Research Fund; Helse Vest; the Norwegian Cancer Society; the Norwegian Research Council; the Ovarian Cancer Research Fund; Nationaal Kankerplan of Belgium; Grant-in-Aid for the Third Term Comprehensive 10-Year Strategy For Cancer Control from the Ministry of Health Labour and Welfare of Japan; the L & S Milken Foundation; the Polish Ministry of Science and Higher Education (4 PO5C 028 14, 2 PO5A 068 27); the Roswell Park Cancer Institute Alliance Foundation; the US National Cancer Institute (K07-CA095666, K07-CA143047,K22-CA138563, N01-CN55424, N01-PC67001, N01-PC067010, N01-PC035137, P01-CA017054, P01-CA087696, P30-CA072720, P50-CA105009, P50-CA136393, R01-CA014089, R01-CA016056, R01-CA017054, R01-CA049449, R01-CA050385, R01-CA054419, R01-CA058598, R01-CA058860, R01-CA061107, R01-CA061132, R01-CA067262, R01-CA071766, R01-CA074850, R01-CA080742, R01-CA080978, R01-CA083918, R01-CA087538, R01-CA092044, R01-095023, R01-CA122443, R01-CA112523, R01-CA114343, R01-CA126841, R01-CA136924, R03-CA113148, R03-CA115195, U01-CA069417, U01-CA071966 and Intramural research funds); the US Army Medical Research and Material Command (DAMD17-01-1-0729, DAMD17-02-1-0666, DAMD17-02-1-0669, W81XWH-07-0449, W81XWH-10-1-02802); the US Public Health Service (PSA-042205); The National Health and Medical Research Council of Australia (199600 and 400281); the German Federal Ministry of Education and Research of Germany Programme of Clinical Biomedical Research (01GB 9401); the State of Baden-Wurttemberg through Medical Faculty of the University of Ulm (P.685); the Minnesota Ovarian Cancer Alliance; the Mayo Foundation; the Fred C. and Katherine B. Andersen Foundation; the Lon V. Smith Foundation (LVS-39420); the Oak Foundation; the OHSU Foundation; the Mermaid I project; the Rudolf-Bartling Foundation; the UK National Institute for Health Research Biomedical Research Centres at the University of Cambridge, Imperial College London, University College Hospital "Womens Health Theme" and the Royal Marsden Hospital; WorkSafeBC 14.
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