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Genome-wide association study identifies the GLDC/IL33 locus associated with survival of osteosarcoma patients

  1. Author:
    Koster, Roelof [ORCID]
    Panagiotou, Orestis A
    Wheeler, William A
    Karlins, Eric
    Gastier-Foster, Julie M
    Caminada de Toledo, Silvia Regina
    Petrilli, Antonio S
    Flanagan, Adrienne M
    Tirabosco, Roberto
    Andrulis, Irene L
    Wunder, Jay S
    Gokgoz, Nalan
    Patiño-Garcia, Ana
    Lecanda, Fernando
    Serra, Massimo
    Hattinger, Claudia
    Picci, Piero
    Scotlandi, Katia
    Thomas, David M
    Ballinger, Mandy L
    Gorlick, Richard
    Barkauskas, Donald A
    Spector, Logan G
    Tucker, Margaret
    Hicks, Belynda
    Yeager, Meredith
    Hoover, Robert N
    Wacholder, Sholom
    Chanock, Stephen J
    Savage, Sharon A
    Mirabello, Lisa
  2. Author Address

    Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA., Information Management Services (IMS), Inc. Rockville, MD, USA., Cancer Genomics Research Laboratory, Leidos Biomedical Research, Frederick National Laboratory for Cancer Research, Frederick, MD, USA., Nationwide Children 39;s Hospital, and The Ohio State University Department of Pathology and Pediatrics, Columbus, OH, USA., Laboratorio de Gen 233;tica, Pediatric Oncology Institute, GRAACC/UNIFESP, S 227;o Paulo, Brazil., UCL Cancer Institute, Huntley Street, London, UK., Royal National Orthopaedic Hospital NHS Trust, Stanmore, Middlesex, UK., Litwin Centre for Cancer Genetics, Samuel Lunenfeld Research Institute, Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada., Department of Pediatrics, University Clinic of Navarra, Universidad de Navarra, Pamplona, Spain., Laboratory of Experimental Oncology, Orthopaedic Rizzoli Institute, Bologna, Italy., Department of Pediatrics, University of Minnesota Minneapolis, MN, 55455, USA., The Kinghorn Cancer Centre, Garvan Institute of Medical Research, Darlinghurst, NSW, Australia., Albert Einstein College of Medicine, The Children 39;s Hospital at Montefiore, New York, NY, USA., Keck School of Medicine, University of Southern California, Los Angeles, California, USA.,
    1. Year: 2018
    2. Date: Apr 15
    3. Epub Date: 2017 12 06
  1. Journal: International journal of cancer
    1. 142
    2. 8
    3. Pages: 1594-1601
  2. Type of Article: Article
  3. ISSN: 0020-7136
  1. Abstract:

    Survival rates for osteosarcoma, the most common primary bone cancer, have changed little over the past three decades and are particularly low for patients with metastatic disease. We conducted a multi-institutional genome-wide association study (GWAS) to identify germline genetic variants associated with overall survival in 632 patients with osteosarcoma including 523 patients of European ancestry and 109 from Brazil. We conducted a time-to-event analysis and estimated hazard ratios (HR) and 95% confidence intervals (CI) using Cox proportional hazards models, with and without adjustment for metastatic disease. The results were combined across the European and Brazilian case sets using a random-effects meta-analysis. The strongest association after meta-analysis, was for rs3765555 at 9p24.1, which was inversely associated with overall survival (HR=1.76; 95% CI 1.41-2.18, P=4.84 × 10-7 ). After imputation across this region, the combined analysis identified two SNPs that reached genome-wide significance. The strongest single association was with rs55933544 (HR=1.9; 95% CI 1.5-2.4; P=1.3 × 10-8 ), which localizes to the GLDC gene, adjacent to the IL33 gene and was consistent across both the European and Brazilian case sets. Using publicly available data, the risk allele was associated with lower expression of IL33 and low expression of IL33 was associated with poor survival in an independent set of patients with osteosarcoma. In conclusion, we have identified the GLDC/IL33 locus on chromosome 9p24.1 as associated with overall survival in patients with osteosarcoma. Further studies are needed to confirm this association and shed light on the biological underpinnings of this susceptibility locus. This article is protected by copyright. All rights reserved. © 2017 UICC.

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External Sources

  1. DOI: 10.1002/ijc.31195
  2. PMID: 29210060
  3. WOS: 000425184800011

Library Notes

  1. Fiscal Year: FY2017-2018
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