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Development and application of a fluorescence protein microarray for detecting serum alpha-fetoprotein in patients with hepatocellular carcinoma

OBJECTIVE: To develop a simple, effective, time-saving and low-cost fluorescence protein microarray method for detecting serum alpha-fetoprotein (AFP) in patients with hepatocellular carcinoma (HCC). METHOD: Non-contact piezoelectric print techniques were applied to fluorescence protein microarray t...

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Detalles Bibliográficos
Autores principales: Zhang, Aiying, Yin, Chengzeng, Wang, Zhenshun, Zhang, Yonghong, Zhao, Yuanshun, Li, Ang, Sun, Huanqin, Lin, Dongdong, Li, Ning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536749/
https://www.ncbi.nlm.nih.gov/pubmed/27885040
http://dx.doi.org/10.1177/0300060516672370
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author Zhang, Aiying
Yin, Chengzeng
Wang, Zhenshun
Zhang, Yonghong
Zhao, Yuanshun
Li, Ang
Sun, Huanqin
Lin, Dongdong
Li, Ning
author_facet Zhang, Aiying
Yin, Chengzeng
Wang, Zhenshun
Zhang, Yonghong
Zhao, Yuanshun
Li, Ang
Sun, Huanqin
Lin, Dongdong
Li, Ning
author_sort Zhang, Aiying
collection PubMed
description OBJECTIVE: To develop a simple, effective, time-saving and low-cost fluorescence protein microarray method for detecting serum alpha-fetoprotein (AFP) in patients with hepatocellular carcinoma (HCC). METHOD: Non-contact piezoelectric print techniques were applied to fluorescence protein microarray to reduce the cost of prey antibody. Serum samples from patients with HCC and healthy control subjects were collected and evaluated for the presence of AFP using a novel fluorescence protein microarray. To validate the fluorescence protein microarray, serum samples were tested for AFP using an enzyme-linked immunosorbent assay (ELISA). RESULTS: A total of 110 serum samples from patients with HCC (n = 65) and healthy control subjects (n = 45) were analysed. When the AFP cut-off value was set at 20 ng/ml, the fluorescence protein microarray had a sensitivity of 91.67% and a specificity of 93.24% for detecting serum AFP. Serum AFP quantified via fluorescence protein microarray had a similar diagnostic performance compared with ELISA in distinguishing patients with HCC from healthy control subjects (area under receiver operating characteristic curve: 0.906 for fluorescence protein microarray; 0.880 for ELISA). CONCLUSION: A fluorescence protein microarray method was developed for detecting serum AFP in patients with HCC.
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spelling pubmed-55367492017-10-03 Development and application of a fluorescence protein microarray for detecting serum alpha-fetoprotein in patients with hepatocellular carcinoma Zhang, Aiying Yin, Chengzeng Wang, Zhenshun Zhang, Yonghong Zhao, Yuanshun Li, Ang Sun, Huanqin Lin, Dongdong Li, Ning J Int Med Res Research Reports OBJECTIVE: To develop a simple, effective, time-saving and low-cost fluorescence protein microarray method for detecting serum alpha-fetoprotein (AFP) in patients with hepatocellular carcinoma (HCC). METHOD: Non-contact piezoelectric print techniques were applied to fluorescence protein microarray to reduce the cost of prey antibody. Serum samples from patients with HCC and healthy control subjects were collected and evaluated for the presence of AFP using a novel fluorescence protein microarray. To validate the fluorescence protein microarray, serum samples were tested for AFP using an enzyme-linked immunosorbent assay (ELISA). RESULTS: A total of 110 serum samples from patients with HCC (n = 65) and healthy control subjects (n = 45) were analysed. When the AFP cut-off value was set at 20 ng/ml, the fluorescence protein microarray had a sensitivity of 91.67% and a specificity of 93.24% for detecting serum AFP. Serum AFP quantified via fluorescence protein microarray had a similar diagnostic performance compared with ELISA in distinguishing patients with HCC from healthy control subjects (area under receiver operating characteristic curve: 0.906 for fluorescence protein microarray; 0.880 for ELISA). CONCLUSION: A fluorescence protein microarray method was developed for detecting serum AFP in patients with HCC. SAGE Publications 2016-11-24 2016-12 /pmc/articles/PMC5536749/ /pubmed/27885040 http://dx.doi.org/10.1177/0300060516672370 Text en © The Author(s) 2016 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Research Reports
Zhang, Aiying
Yin, Chengzeng
Wang, Zhenshun
Zhang, Yonghong
Zhao, Yuanshun
Li, Ang
Sun, Huanqin
Lin, Dongdong
Li, Ning
Development and application of a fluorescence protein microarray for detecting serum alpha-fetoprotein in patients with hepatocellular carcinoma
title Development and application of a fluorescence protein microarray for detecting serum alpha-fetoprotein in patients with hepatocellular carcinoma
title_full Development and application of a fluorescence protein microarray for detecting serum alpha-fetoprotein in patients with hepatocellular carcinoma
title_fullStr Development and application of a fluorescence protein microarray for detecting serum alpha-fetoprotein in patients with hepatocellular carcinoma
title_full_unstemmed Development and application of a fluorescence protein microarray for detecting serum alpha-fetoprotein in patients with hepatocellular carcinoma
title_short Development and application of a fluorescence protein microarray for detecting serum alpha-fetoprotein in patients with hepatocellular carcinoma
title_sort development and application of a fluorescence protein microarray for detecting serum alpha-fetoprotein in patients with hepatocellular carcinoma
topic Research Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536749/
https://www.ncbi.nlm.nih.gov/pubmed/27885040
http://dx.doi.org/10.1177/0300060516672370
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