FOXP3 autoantibody as a potential early prognostic serum biomarker in patients with cervical cancer

Verfasser / Beitragende:
[Shuang Xu, Mingmei Huangfu, Xueli Jia, Xiaowei Song, Baosheng Sun, Kuang-Hui Lee, Linlin Liu, Shilong Sun]
Ort, Verlag, Jahr:
2015
Enthalten in:
International Journal of Clinical Oncology, 20/5(2015-10-01), 982-988
Format:
Artikel (online)
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024 7 0 |a 10.1007/s10147-015-0797-4  |2 doi 
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245 0 0 |a FOXP3 autoantibody as a potential early prognostic serum biomarker in patients with cervical cancer  |h [Elektronische Daten]  |c [Shuang Xu, Mingmei Huangfu, Xueli Jia, Xiaowei Song, Baosheng Sun, Kuang-Hui Lee, Linlin Liu, Shilong Sun] 
520 3 |a Background: Overexpression of tumor-associated antigens has been reported in many types of cancer and may trigger secretion of their autoantibodies. The present work was designed to test whether circulating antibody to FOXP3 protein-derived antigens was altered in early cervical cancer and cervical benign tumors. Methods: A total of 141 patients with cervical cancer, 133 patients with cervical benign tumors and 148 healthy age-matched volunteers were recruited. The level of circulating anti-FOXP3 IgG antibody was tested using an enzyme-linked immunosorbent assay developed in-house with linear peptide antigens derived from FOXP3 protein. The linear peptide antigens were designed according to the computational prediction of HLA-II epitopes. Results: Student's t test showed that anti-FOXP3 IgG in the malignant tumor group and the benign tumor group was significantly higher than in the control group (t=6.127, p<0.001; t=2.704, p=0.007). In addition, patients with stage I cervical cancer (t=2.968, p=0.003) had a significantly higher level of FOXP3 autoantibodies than patients with benign tumors. The sensitivity against >90% specificity was 20.6% with an interassay deviation of 11.7% in the cervical cancer group. Based on a cut-off value determined by the 98th percentile of the control group IgG levels, the anti-FOXP3 IgG positivity was 2.1% in patients with cervical cancer compared to 2.0% in the health controls (chi-squared=0.004, p=0.952, OR=1.051, 95% CI 0.209-5.295). Conclusion: The circulating autoantibody to FOXP3 reflecting the continuous development of the cervical lesion, may be a potential biomarker with early prognostic values for cervical cancer. 
540 |a Japan Society of Clinical Oncology, 2015 
690 7 |a Autoantibody  |2 nationallicence 
690 7 |a Biomarkers  |2 nationallicence 
690 7 |a Cervical cancer  |2 nationallicence 
690 7 |a FOXP3  |2 nationallicence 
690 7 |a Tumor immunity  |2 nationallicence 
700 1 |a Xu  |D Shuang  |u Department of Radiotherapy, Second Hospital of Jilin University, 130041, Changchun, China  |4 aut 
700 1 |a Huangfu  |D Mingmei  |u Department of Radiotherapy, Second Hospital of Jilin University, 130041, Changchun, China  |4 aut 
700 1 |a Jia  |D Xueli  |u Department of Radiotherapy, Second Hospital of Jilin University, 130041, Changchun, China  |4 aut 
700 1 |a Song  |D Xiaowei  |u Ministry of Health Key Laboratory of Radiobiology, Jilin University, 130021, Changchun, China  |4 aut 
700 1 |a Sun  |D Baosheng  |u Department of Radiotherapy, Tumor Hospital of Jilin Province, 130012, Changchun, China  |4 aut 
700 1 |a Lee  |D Kuang-Hui  |u Pei-Ling Guan-Si Hospital, Hsin-Fu Kuansi Township, 30647, Hsinchu County, Taiwan  |4 aut 
700 1 |a Liu  |D Linlin  |u Department of Radiotherapy, Second Hospital of Jilin University, 130041, Changchun, China  |4 aut 
700 1 |a Sun  |D Shilong  |u Ministry of Health Key Laboratory of Radiobiology, Jilin University, 130021, Changchun, China  |4 aut 
773 0 |t International Journal of Clinical Oncology  |d Springer Japan  |g 20/5(2015-10-01), 982-988  |x 1341-9625  |q 20:5<982  |1 2015  |2 20  |o 10147 
856 4 0 |u https://doi.org/10.1007/s10147-015-0797-4  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1007/s10147-015-0797-4  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Xu  |D Shuang  |u Department of Radiotherapy, Second Hospital of Jilin University, 130041, Changchun, China  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Huangfu  |D Mingmei  |u Department of Radiotherapy, Second Hospital of Jilin University, 130041, Changchun, China  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Jia  |D Xueli  |u Department of Radiotherapy, Second Hospital of Jilin University, 130041, Changchun, China  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Song  |D Xiaowei  |u Ministry of Health Key Laboratory of Radiobiology, Jilin University, 130021, Changchun, China  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Sun  |D Baosheng  |u Department of Radiotherapy, Tumor Hospital of Jilin Province, 130012, Changchun, China  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Lee  |D Kuang-Hui  |u Pei-Ling Guan-Si Hospital, Hsin-Fu Kuansi Township, 30647, Hsinchu County, Taiwan  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Liu  |D Linlin  |u Department of Radiotherapy, Second Hospital of Jilin University, 130041, Changchun, China  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Sun  |D Shilong  |u Ministry of Health Key Laboratory of Radiobiology, Jilin University, 130021, Changchun, China  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t International Journal of Clinical Oncology  |d Springer Japan  |g 20/5(2015-10-01), 982-988  |x 1341-9625  |q 20:5<982  |1 2015  |2 20  |o 10147