4.5 Article

SOX2 Autoantibodies As Noninvasive Serum Biomarker for Breast Carcinoma

Journal

CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
Volume 21, Issue 11, Pages 2043-2047

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1055-9965.EPI-12-0498

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Funding

  1. National High Technology Research and Development Program of China (863 Program) [2011AA02A116]
  2. Peking Union Medical College Innovation Fund for Graduates [2010-1002-002]

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Background: A clear association has been established between antibodies to the transcription factor sex-determining region Y (SRY)-box 2 (S0X2) and small cell lung cancer. In light of the pathologic role of SOX2 and its aberrant expression in breast cancer, we measured serum SOX2 autoantibodies (SOX2-Abs) in breast cancer patients. Methods: The presence of SOX2-Abs was determined by an indirect enzyme-linked immunosorbent assay (ELISA) in sera from 282 patients with breast cancer, 78 patients with benign breast disease, and 194 healthy women. Results: SOX2-Abs were more prevalent in patients with breast cancer (18.4%) compared with healthy women (2.6%, P < 0.0001), and patients with benign breast disease (6.4%, P = 0.011). The concentrations of circulating SOX2-Abs were found to discriminate between breast cancer patients and healthy controls (P < 0.001) and between breast cancer patients and those with benign breast disease (P < 0.001). In addition, measurement of SOX2-Abs was more effective than assays of serum tissue polypeptide-specific antigen, carcinoembryonic antigen, carbohydrate antigen (CA) 125, and CA 15-3 in distinguishing between malignant and benign breast disease. In breast cancer patients, the prevalence of SOX2-Abs was associated with a higher tumor grade (P = 0.021) and positive nodal status (P = 0.021). Conclusion: The presence of SOX2-Abs in breast cancer may be of clinical value. Impact: This study provides the first evidence for the presence of circulating SOX2-Abs in breast cancer and shows their potential clinical application. Cancer Epidemiol Biomarkers Prev; 21(11); 2043-7. (C)2012 AACR.

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