Evaluation of glycomic profiling as a diagnostic biomarker for epithelial ovarian cancer
Autor: | Kyoungmi Kim, Lauren M. Dimapasoc, Gary S. Leiserowitz, Uyen Thao Nguyen, Cynthia C. Williams, Sureyya Ozcan, Suzanne Miyamoto, Carol Stroble, Carlito B. Lebrilla, Sandra L. Taylor, L. Renee Ruhaak |
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Přispěvatelé: | OpenMETU |
Rok vydání: | 2014 |
Předmět: |
Serum
Oncology Identification Glycosylation endocrine system diseases Epidemiology Mass-spectrometry N-glycans Carcinoma Ovarian Epithelial Bioinformatics Medical and Health Sciences Cohort Studies Neoplasms Ovarian Epithelial Disease Neoplasms Glandular and Epithelial Glycan biomarkers Biomarker discovery Glycomics Cancer Ovarian Neoplasms screening and diagnosis Tumor biology Glycobiology Glandular and Epithelial Middle Aged female genital diseases and pregnancy complications Ovarian Cancer Detection Female 4.2 Evaluation of markers and technologies endocrine system Glycan medicine.medical_specialty Annotation Gynecologic oncology Discovery Article Rare Diseases Clinical Research Internal medicine Carcinoma medicine Biomarkers Tumor Humans Prevention Case-control study medicine.disease 4.1 Discovery and preclinical testing of markers and technologies carbohydrates (lipids) Case-Control Studies biology.protein Ovarian cancer Biomarkers |
Zdroj: | Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, vol 23, iss 4 |
ISSN: | 1538-7755 |
Popis: | Background: Prior studies suggested that glycans were differentially expressed in patients with ovarian cancer and controls. We hypothesized that glycan-based biomarkers might serve as a diagnostic test for ovarian cancer and evaluated the ability of glycans to distinguish ovarian cancer cases from matched controls. Methods: Serum samples were obtained from the tissue-banking repository of the Gynecologic Oncology Group, and included healthy female controls (n = 100), women diagnosed with low malignant potential (LMP) tumors (n = 52), and epithelial ovarian cancers (EOC) cases (n = 147). Cases and controls were matched on age at enrollment within ±5 years. Serum samples were analyzed by glycomics analysis to detect abundance differences in glycan expression levels. A two-stage procedure was carried out for biomarker discovery and validation. Candidate classifiers of glycans that separated cases from controls were developed using a training set in the discovery phase and the classification performance of the candidate classifiers was assessed using independent test samples that were not used in discovery. Results: The patterns of glycans showed discriminatory power for distinguishing EOC and LMP cases from controls. Candidate glycan-based biomarkers developed on a training set (sensitivity, 86% and specificity, 95.8% for distinguishing EOC from controls through leave-one-out cross-validation) confirmed their potential use as a detection test using an independent test set (sensitivity, 70% and specificity, 86.5%). Conclusion: Formal investigations of glycan biomarkers that distinguish cases and controls show great promise for an ovarian cancer diagnostic test. Further validation of a glycan-based test for detection of ovarian cancer is warranted. Impact: An emerging diagnostic test based on the knowledge gained from understanding the glycobiology should lead to an assay that improves sensitivity and specificity and allows for early detection of ovarian cancer. Cancer Epidemiol Biomarkers Prev; 23(4); 611–21. ©2014 AACR. |
Databáze: | OpenAIRE |
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