A cis-eQTL genetic variant of the cancer–testis gene CCDC116 is associated with risk of multiple cancers

Recent studies have found that cancer–testis (CT) genes, which are expressed predominantly in germ and cancer cells, may be candidate cancer drivers. Because of their crucial roles, genetic variants in these genes may contribute to the development of cancer. Here, we systematically evaluated associations of common variants in CT genes and their promoters for the risk of lung cancer in our initial GWAS (2331 cases and 3077 controls), followed by in silico replication using additional 10,512 lung cancer cases and 9562 controls. We found a significant association between rs3747093 located in the CCDC116 promoter and lung cancer risk (OR = 0.91, Pmeta = 7.81 × 10−6). Although CCDC116 was expressed at lower levels in somatic tissues compared to the testis, the protective allele A of rs3747093 was associated with decreased CCDC116 expression in many normal tissues, including the lung (P = 8.1 × 10−13). We subsequently genotyped this variant in another four commonly diagnosed cancers (gastric, esophageal, colorectal, and breast cancers), as we found expression quantitative trait locus (eQTL) signals for rs3747093 and CCDC116 in their corresponding normal tissues. Interestingly, we observed consistent associations between rs3747093 and multiple cancers (gastric cancer: OR = 0.85, P = 2.21 × 10−4; esophageal cancer: OR = 0.91, P = 2.57 × 10−2; colorectal cancer: OR = 0.80, P = 1.85 × 10−6; and breast cancer: OR = 0.87, P = 1.55 × 10−3). Taken together, the A allele of rs3747093 showed significant protective effects on cancer risk (OR = 0.88, Ppool = 6.52 × 10−13) in an Asian population. Moreover, our findings suggest that low abundance expression of CT genes in normal tissues may also contribute to tumorigenesis, providing a new mechanism of CT genes in the development of cancer.

[1]  Tariq Ahmad,et al.  Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci , 2010, Nature Genetics.

[2]  Joseph K. Pickrell Joint analysis of functional genomic data and genome-wide association studies of 18 human traits , 2013, bioRxiv.

[3]  Jedd D. Wolchok,et al.  Immunologic correlates of the abscopal effect in a patient with melanoma. , 2012, The New England journal of medicine.

[4]  P. Sham,et al.  Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians. , 2013, American journal of human genetics.

[5]  John T. Powers,et al.  Multiple mechanisms disrupt the let-7 microRNA family in neuroblastoma , 2016, Nature.

[6]  P. Chomez,et al.  A gene encoding an antigen recognized by cytolytic T lymphocytes on a human melanoma. , 1991, Science.

[7]  Lloyd J. Old,et al.  Cancer/testis antigens, gametogenesis and cancer , 2005, Nature Reviews Cancer.

[8]  Victor V Lobanenkov,et al.  BORIS/CTCFL-mediated transcriptional regulation of the hTERT telomerase gene in testicular and ovarian tumor cells , 2010, Nucleic acids research.

[9]  Henrik Gronberg,et al.  A genome-wide search for loci interacting with known prostate cancer risk-associated genetic variants. , 2012, Carcinogenesis.

[10]  T. Stearns,et al.  Proteomic analysis of mammalian sperm cells identifies new components of the centrosome , 2014, Journal of Cell Science.

[11]  C. Carlson,et al.  Genome-Wide Diet-Gene Interaction Analyses for Risk of Colorectal Cancer , 2014, PLoS genetics.

[12]  P. Deloukas,et al.  Multiple common variants for celiac disease influencing immune gene expression , 2010, Nature Genetics.

[13]  D. Clayton,et al.  Genome-wide association studies: theoretical and practical concerns , 2005, Nature Reviews Genetics.

[14]  B. Ouyang,et al.  A Novel Testis-Specific Gene, Ccdc136, Is Required for Acrosome Formation and Fertilization in Mice , 2016, Reproductive Sciences.

[15]  R. Kesterson,et al.  Coiled-coil domain containing 42 (Ccdc42) is necessary for proper sperm development and male fertility in the mouse. , 2016, Developmental biology.

[16]  P. Gaffney,et al.  A functional haplotype of UBE2L3 confers risk for systemic lupus erythematosus , 2012, Genes and Immunity.

[17]  Ying Wang,et al.  A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. , 2009, American journal of human genetics.

[18]  R. Stallings,et al.  LIN28B induces neuroblastoma and enhances MYCN levels via let-7 suppression , 2012, Nature Genetics.

[19]  Ming Chen,et al.  CCDC62/ERAP75 functions as a coactivator to enhance estrogen receptor beta-mediated transactivation and target gene expression in prostate cancer cells. , 2009, Carcinogenesis.

[20]  Robert M. Plenge,et al.  Meta-Analysis of Genome-Wide Association Studies in Celiac Disease and Rheumatoid Arthritis Identifies Fourteen Non-HLA Shared Loci , 2011, PLoS genetics.

[21]  M. Thun,et al.  The American Cancer Society Cancer Prevention Study II Nutrition Cohort , 2002, Cancer.

[22]  K. Taylor,et al.  Genome-Wide Association , 2007, Diabetes.

[23]  Annette Lee,et al.  Differential Genetic Associations for Systemic Lupus Erythematosus Based on Anti–dsDNA Autoantibody Production , 2011, PLoS genetics.

[24]  F. Collins,et al.  Potential etiologic and functional implications of genome-wide association loci for human diseases and traits , 2009, Proceedings of the National Academy of Sciences.

[25]  Hongbing Shen,et al.  Systematic identification of genes with a cancer-testis expression pattern in 19 cancer types , 2016, Nature Communications.

[26]  David C. Wilson,et al.  Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease , 2012, Nature.

[27]  Hongtae Kim,et al.  Factors forming the BRCA1-A complex orchestrate BRCA1 recruitment to the sites of DNA damage. , 2016, Acta biochimica et biophysica Sinica.

[28]  Meta-Analysis of Genome-Wide Association Studies in Celiac Disease and Rheumatoid Arthritis Identifies Fourteen Non-HLA Shared Loci , 2011, PLoS genetics.

[29]  A. Jemal,et al.  Global cancer statistics , 2011, CA: a cancer journal for clinicians.

[30]  Oliver Hofmann,et al.  Genome-wide analysis of cancer/testis gene expression , 2008, Proceedings of the National Academy of Sciences.

[31]  P. Gönczy Centrosomes and cancer: revisiting a long-standing relationship , 2015, Nature Reviews Cancer.

[32]  E. Pukkala,et al.  Increased risk of cancer in patients with systemic lupus erythematosus. , 1992, Annals of the rheumatic diseases.

[33]  Jun S. Liu,et al.  Genetics of rheumatoid arthritis contributes to biology and drug discovery , 2013 .

[34]  M. Karin,et al.  Immunity, Inflammation, and Cancer , 2010, Cell.

[35]  A. Jemal,et al.  Global Cancer Statistics , 2011 .

[36]  J. Rioux,et al.  Genetic association analyses implicate aberrant regulation of innate and adaptive immunity genes in the pathogenesis of systemic lupus erythematosus , 2015, Nature Genetics.

[37]  P. Bruggen,et al.  Tumor antigens recognized by T lymphocytes. , 1994, Annual review of immunology.

[38]  J J Gómez-Reino Carnota,et al.  [Genetics of rheumatoid arthritis]. , 2000, Medicina clinica.

[39]  Ying Wang,et al.  Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus , 2009, Nature Genetics.

[40]  John T. Powers,et al.  Lin28b is sufficient to drive liver cancer and necessary for its maintenance in murine models. , 2014, Cancer cell.

[41]  A. Jemal,et al.  Global cancer statistics, 2012 , 2015, CA: a cancer journal for clinicians.

[42]  K. Lange,et al.  Prioritizing GWAS results: A review of statistical methods and recommendations for their application. , 2010, American journal of human genetics.

[43]  Robert N Hoover,et al.  Methods for etiologic and early marker investigations in the PLCO trial. , 2005, Mutation research.

[44]  S. Wacholder,et al.  Environment And Genetics in Lung cancer Etiology (EAGLE) study: An integrative population-based case-control study of lung cancer , 2008, BMC public health.

[45]  T. Spector,et al.  UBE2L3 Polymorphism Amplifies NF-κB Activation and Promotes Plasma Cell Development, Linking Linear Ubiquitination to Multiple Autoimmune Diseases , 2015, American journal of human genetics.

[46]  A. Ashworth,et al.  Genomic Complexity Profiling Reveals That HORMAD1 Overexpression Contributes to Homologous Recombination Deficiency in Triple-Negative Breast Cancers. , 2015, Cancer discovery.

[47]  J. Malm,et al.  Cyclin A1 and P450 Aromatase Promote Metastatic Homing and Growth of Stem-like Prostate Cancer Cells in the Bone Marrow. , 2016, Cancer research.

[48]  Carmen Rodriguez,et al.  The American Cancer Society Cancer Prevention Study II Nutrition Cohort , 2002, Cancer.

[49]  C. Lupp Host–microbe interactions , 2007, Nature.

[50]  Wen Tan,et al.  A genome-wide association study identifies two new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese , 2011, Nature Genetics.

[51]  P. Visscher,et al.  Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets , 2016, Nature Genetics.

[52]  John T. Powers,et al.  Lin28 Enhances Tumorigenesis and is Associated With Advanced Human Malignancies , 2009, Nature Genetics.

[53]  B. Qian,et al.  Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia , 2012, Nature Genetics.