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Published in: Tumor Biology 3/2013

01-06-2013 | Research Article

Circulating autoantibody to FOXP3 may be a potential biomarker for esophageal squamous cell carcinoma

Authors: Leiguang Ye, Songlei Guan, Cong Zhang, Kuang-Hui Lee, Shilong Sun, Jun Wei, Baogang Liu

Published in: Tumor Biology | Issue 3/2013

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Abstract

The present study was undertaken to develop a relatively quantitative enzyme-linked immunosorbent assay (ELISA) in-house using human leukocyte antigen class II-restricted epitopes in order to test circulating autoantibodies to human forkhead/winged helix transcription factor (FOXP3) as a biomarker for esophageal cancer. A total of 97 patients with esophageal squamous cell carcinoma (ESCC) and 227 healthy subjects were recruited for this study, and their plasma samples were collected for antibody analysis with the ELISA approach. Student’s t test showed that the anti-FOXP3 IgG antibody levels were significantly higher in the patient group than the control group (t = 6.23, P < 0.0001). Based on a cutoff value determined by the mean + 3SD of control IgG levels, the positive rate was 5.15 % in patients with ESCC as compared to 0.88 % in control subjects (X 2 = 6.53, P = 0.019, OR = 5.85, 95 % CI 1.12–30.67), in which patients at stage I had the highest positivity (11.54 %, X 2 = 12.15, P = 0.0005, OR = 13.10, 95 % CI 2.09–82.04). The sensitivity against >95 % specificity was 22.7 % for the IgG assay with an inter-assay deviation of 13.35 %. This work suggests that circulating IgG autoantibody to FOXP3 may be a potential biomarker for early diagnosis of esophageal cancer.
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Metadata
Title
Circulating autoantibody to FOXP3 may be a potential biomarker for esophageal squamous cell carcinoma
Authors
Leiguang Ye
Songlei Guan
Cong Zhang
Kuang-Hui Lee
Shilong Sun
Jun Wei
Baogang Liu
Publication date
01-06-2013
Publisher
Springer Netherlands
Published in
Tumor Biology / Issue 3/2013
Print ISSN: 1010-4283
Electronic ISSN: 1423-0380
DOI
https://doi.org/10.1007/s13277-013-0729-8

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