| Literature DB >> 26137272 |
Cairen Chen1, Yile Huang1, Cong Zhang2, Tong Liu3, H E Zheng1, Shuli Wan1, Shilong Sun2, Qingyong Meng1, Yubing Chen4, Jun Wei5.
Abstract
Overexpression of the p16 protein has been reported in breast cancer and may trigger the secretion of antibodies against itself. Circulating anti-p16 antibodies that were detected with a recombinant protein have been reported in breast cancer. The present study was designed to determine whether the levels of circulating IgG antibody to p16 protein-derived linear antigens are altered in breast cancer. An enzyme-linked immunosorbent assay (ELISA) was developed in-house to determine circulating IgG against peptide antigens derived from the p16 protein in 152 female breast cancer patients and 160 healthy female subjects. The Student's T-test revealed that breast cancer patients exhibited significantly higher levels of anti-p16 IgG antibody compared to control subjects (T=2.02, P=0.045). In addition, ductal cancer appeared to be the main type contributing to the increased levels of circulating anti-p16 antibodies (T=2.08, P=0.038). Of all four stages of breast cancer, stage I was associated with the highest levels of IgG antibody (T=2.02, P=0.045) and receiver operating characteristic (ROC) analysis demonstrated that the area under the ROC curve was 0.74 (95% confidence interval: 0.65-083) and that the sensitivity against a specificity of 90% was 30.3%. Therefore, the levels of circulating IgG antibody to the p16 protein may be a potential biomarker for early diagnosis of breast cancer.Entities:
Keywords: autoantibody; biomarker; breast cancer; p16 protein; tumor immunity
Year: 2015 PMID: 26137272 PMCID: PMC4471576 DOI: 10.3892/mco.2015.485
Source DB: PubMed Journal: Mol Clin Oncol ISSN: 2049-9450