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Identification of serum proteins AHSG, FGA and APOA-I as diagnostic biomarkers for gastric cancer

BACKGROUND: The development of clinically accessible biomarkers is critical for the early diagnosis of gastric cancer (GC) in patients. High-throughput proteomics techniques could not only effectively generate a serum peptide profile but also provide a new approach to identify potentially diagnostic...

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Autores principales: Shi, Feiyu, Wu, Hong, Qu, Kai, Sun, Qi, Li, Fanni, Shi, Chengxin, Li, Yaguang, Xiong, Xiaofan, Qin, Qian, Yu, Tianyu, Jin, Xin, Cheng, Liang, Wei, Qingxia, Li, Yingchao, She, Junjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5925839/
https://www.ncbi.nlm.nih.gov/pubmed/29719494
http://dx.doi.org/10.1186/s12014-018-9194-0
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author Shi, Feiyu
Wu, Hong
Qu, Kai
Sun, Qi
Li, Fanni
Shi, Chengxin
Li, Yaguang
Xiong, Xiaofan
Qin, Qian
Yu, Tianyu
Jin, Xin
Cheng, Liang
Wei, Qingxia
Li, Yingchao
She, Junjun
author_facet Shi, Feiyu
Wu, Hong
Qu, Kai
Sun, Qi
Li, Fanni
Shi, Chengxin
Li, Yaguang
Xiong, Xiaofan
Qin, Qian
Yu, Tianyu
Jin, Xin
Cheng, Liang
Wei, Qingxia
Li, Yingchao
She, Junjun
author_sort Shi, Feiyu
collection PubMed
description BACKGROUND: The development of clinically accessible biomarkers is critical for the early diagnosis of gastric cancer (GC) in patients. High-throughput proteomics techniques could not only effectively generate a serum peptide profile but also provide a new approach to identify potentially diagnostic and prognostic biomarkers for cancer patients. METHODS: In this study, we aim to identify potentially discriminating serum biomarkers for GC. In the discovery cohort, we screened potential biomarkers using magnetic-bead-based purification and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry in 64 samples from 32 GC patients that were taken both pre- and post-operatively and 30 healthy volunteers that served as controls. In the validation cohort, the expression patterns and diagnostic values of serum FGA, AHSG and APOA-I were further confirmed by ELISA in 42 paired GC patients (pre- and post-operative samples from 16 patients with pathologic stage I/II and 26 with stage III/IV), 30 colorectal cancer patients, 30 hepatocellular carcinoma patients, and 28 healthy volunteers. RESULTS: ClinProTools software was used and annotated 107 peptides, 12 of which were differentially expressed among three groups (P < 0.0001, fold > 1.5). These 12 peptide peaks were further identified as FGA, AHSG, APOA-I, HBB, TXNRD1, GSPT2 and CAKP5. ELISA data suggested that the serum levels of FGA, AHSG and APOA-I in GC patients were significantly different compared with healthy controls and had favorable diagnostic values for GC patients. Moreover, we found that the serum levels of these three proteins were associated with TNM stages and could reflect tumor burden. CONCLUSION: Our findings suggested that FGA, AHSG and APOA-I might be potential serum biomarkers for GC diagnosis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12014-018-9194-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-59258392018-05-01 Identification of serum proteins AHSG, FGA and APOA-I as diagnostic biomarkers for gastric cancer Shi, Feiyu Wu, Hong Qu, Kai Sun, Qi Li, Fanni Shi, Chengxin Li, Yaguang Xiong, Xiaofan Qin, Qian Yu, Tianyu Jin, Xin Cheng, Liang Wei, Qingxia Li, Yingchao She, Junjun Clin Proteomics Research BACKGROUND: The development of clinically accessible biomarkers is critical for the early diagnosis of gastric cancer (GC) in patients. High-throughput proteomics techniques could not only effectively generate a serum peptide profile but also provide a new approach to identify potentially diagnostic and prognostic biomarkers for cancer patients. METHODS: In this study, we aim to identify potentially discriminating serum biomarkers for GC. In the discovery cohort, we screened potential biomarkers using magnetic-bead-based purification and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry in 64 samples from 32 GC patients that were taken both pre- and post-operatively and 30 healthy volunteers that served as controls. In the validation cohort, the expression patterns and diagnostic values of serum FGA, AHSG and APOA-I were further confirmed by ELISA in 42 paired GC patients (pre- and post-operative samples from 16 patients with pathologic stage I/II and 26 with stage III/IV), 30 colorectal cancer patients, 30 hepatocellular carcinoma patients, and 28 healthy volunteers. RESULTS: ClinProTools software was used and annotated 107 peptides, 12 of which were differentially expressed among three groups (P < 0.0001, fold > 1.5). These 12 peptide peaks were further identified as FGA, AHSG, APOA-I, HBB, TXNRD1, GSPT2 and CAKP5. ELISA data suggested that the serum levels of FGA, AHSG and APOA-I in GC patients were significantly different compared with healthy controls and had favorable diagnostic values for GC patients. Moreover, we found that the serum levels of these three proteins were associated with TNM stages and could reflect tumor burden. CONCLUSION: Our findings suggested that FGA, AHSG and APOA-I might be potential serum biomarkers for GC diagnosis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12014-018-9194-0) contains supplementary material, which is available to authorized users. BioMed Central 2018-04-30 /pmc/articles/PMC5925839/ /pubmed/29719494 http://dx.doi.org/10.1186/s12014-018-9194-0 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Shi, Feiyu
Wu, Hong
Qu, Kai
Sun, Qi
Li, Fanni
Shi, Chengxin
Li, Yaguang
Xiong, Xiaofan
Qin, Qian
Yu, Tianyu
Jin, Xin
Cheng, Liang
Wei, Qingxia
Li, Yingchao
She, Junjun
Identification of serum proteins AHSG, FGA and APOA-I as diagnostic biomarkers for gastric cancer
title Identification of serum proteins AHSG, FGA and APOA-I as diagnostic biomarkers for gastric cancer
title_full Identification of serum proteins AHSG, FGA and APOA-I as diagnostic biomarkers for gastric cancer
title_fullStr Identification of serum proteins AHSG, FGA and APOA-I as diagnostic biomarkers for gastric cancer
title_full_unstemmed Identification of serum proteins AHSG, FGA and APOA-I as diagnostic biomarkers for gastric cancer
title_short Identification of serum proteins AHSG, FGA and APOA-I as diagnostic biomarkers for gastric cancer
title_sort identification of serum proteins ahsg, fga and apoa-i as diagnostic biomarkers for gastric cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5925839/
https://www.ncbi.nlm.nih.gov/pubmed/29719494
http://dx.doi.org/10.1186/s12014-018-9194-0
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