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Elevated serum eotaxin and IP‐10 levels as potential biomarkers for the detection of esophageal squamous cell carcinoma

BACKGROUND AND AIMS: Esophageal squamous cell cancer (ESCC) is one of the leading malignant cancers with a high incidence and mortality. Exploring novel serum biomarkers will help improve the management and monitoring of ESCC. METHODS: In the present study, we first used a ProcartaPlex Array to scre...

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Autores principales: Chang, Chen, Wang, Min‐Jie, Bi, Xiao‐Feng, Fan, Zhi‐Yuan, Feng, Dan, Cai, Hong‐Qing, Zhang, Yu, Xu, Xin, Cai, Yan, Qi, Jun, Wei, Wen‐Qiang, Hao, Jia‐Jie, Wang, Ming‐Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8418505/
https://www.ncbi.nlm.nih.gov/pubmed/34288108
http://dx.doi.org/10.1002/jcla.23904
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author Chang, Chen
Wang, Min‐Jie
Bi, Xiao‐Feng
Fan, Zhi‐Yuan
Feng, Dan
Cai, Hong‐Qing
Zhang, Yu
Xu, Xin
Cai, Yan
Qi, Jun
Wei, Wen‐Qiang
Hao, Jia‐Jie
Wang, Ming‐Rong
author_facet Chang, Chen
Wang, Min‐Jie
Bi, Xiao‐Feng
Fan, Zhi‐Yuan
Feng, Dan
Cai, Hong‐Qing
Zhang, Yu
Xu, Xin
Cai, Yan
Qi, Jun
Wei, Wen‐Qiang
Hao, Jia‐Jie
Wang, Ming‐Rong
author_sort Chang, Chen
collection PubMed
description BACKGROUND AND AIMS: Esophageal squamous cell cancer (ESCC) is one of the leading malignant cancers with a high incidence and mortality. Exploring novel serum biomarkers will help improve the management and monitoring of ESCC. METHODS: In the present study, we first used a ProcartaPlex Array to screen for serum proteins that were increased in 40 ESCC patients compared with matched normal controls; we found that eight proteins (IL‐2, IL‐5, IP‐10, IL‐8, eotaxin, TNF‐α, HGF, and MIP‐1b) had higher serum levels in ESCC patients than in normal controls. We further verified the clinical relevance of the candidate biomarkers with a larger sample of sera. RESULTS: In the 174 tested ESCC patients and 189 normal controls, the serum levels of eotaxin and IP‐10 were significantly higher in patients than in normal controls (p = 0.0038, 0.0031). In particular, these two proteins were also elevated in the sera of patients with early‐stage (0‐IIA) ESCC (p = 0.0041, 0.0412). When combining CEA and CYFRA21‐1 (in use clinically) with eotaxin or IP‐10, the effectiveness of detecting ESCC was superior to that of CEA and/or CYFRA21‐1 alone. Moreover, the serum level of eotaxin dropped significantly after surgical resection of primary tumors compared with that in preoperative ESCC samples (p < 0.001). CONCLUSIONS: The data suggest that serum eotaxin and IP‐10 might be potential biomarkers for the detection of ESCC.
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spelling pubmed-84185052021-09-08 Elevated serum eotaxin and IP‐10 levels as potential biomarkers for the detection of esophageal squamous cell carcinoma Chang, Chen Wang, Min‐Jie Bi, Xiao‐Feng Fan, Zhi‐Yuan Feng, Dan Cai, Hong‐Qing Zhang, Yu Xu, Xin Cai, Yan Qi, Jun Wei, Wen‐Qiang Hao, Jia‐Jie Wang, Ming‐Rong J Clin Lab Anal Research Articles BACKGROUND AND AIMS: Esophageal squamous cell cancer (ESCC) is one of the leading malignant cancers with a high incidence and mortality. Exploring novel serum biomarkers will help improve the management and monitoring of ESCC. METHODS: In the present study, we first used a ProcartaPlex Array to screen for serum proteins that were increased in 40 ESCC patients compared with matched normal controls; we found that eight proteins (IL‐2, IL‐5, IP‐10, IL‐8, eotaxin, TNF‐α, HGF, and MIP‐1b) had higher serum levels in ESCC patients than in normal controls. We further verified the clinical relevance of the candidate biomarkers with a larger sample of sera. RESULTS: In the 174 tested ESCC patients and 189 normal controls, the serum levels of eotaxin and IP‐10 were significantly higher in patients than in normal controls (p = 0.0038, 0.0031). In particular, these two proteins were also elevated in the sera of patients with early‐stage (0‐IIA) ESCC (p = 0.0041, 0.0412). When combining CEA and CYFRA21‐1 (in use clinically) with eotaxin or IP‐10, the effectiveness of detecting ESCC was superior to that of CEA and/or CYFRA21‐1 alone. Moreover, the serum level of eotaxin dropped significantly after surgical resection of primary tumors compared with that in preoperative ESCC samples (p < 0.001). CONCLUSIONS: The data suggest that serum eotaxin and IP‐10 might be potential biomarkers for the detection of ESCC. John Wiley and Sons Inc. 2021-07-21 /pmc/articles/PMC8418505/ /pubmed/34288108 http://dx.doi.org/10.1002/jcla.23904 Text en © 2021 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Chang, Chen
Wang, Min‐Jie
Bi, Xiao‐Feng
Fan, Zhi‐Yuan
Feng, Dan
Cai, Hong‐Qing
Zhang, Yu
Xu, Xin
Cai, Yan
Qi, Jun
Wei, Wen‐Qiang
Hao, Jia‐Jie
Wang, Ming‐Rong
Elevated serum eotaxin and IP‐10 levels as potential biomarkers for the detection of esophageal squamous cell carcinoma
title Elevated serum eotaxin and IP‐10 levels as potential biomarkers for the detection of esophageal squamous cell carcinoma
title_full Elevated serum eotaxin and IP‐10 levels as potential biomarkers for the detection of esophageal squamous cell carcinoma
title_fullStr Elevated serum eotaxin and IP‐10 levels as potential biomarkers for the detection of esophageal squamous cell carcinoma
title_full_unstemmed Elevated serum eotaxin and IP‐10 levels as potential biomarkers for the detection of esophageal squamous cell carcinoma
title_short Elevated serum eotaxin and IP‐10 levels as potential biomarkers for the detection of esophageal squamous cell carcinoma
title_sort elevated serum eotaxin and ip‐10 levels as potential biomarkers for the detection of esophageal squamous cell carcinoma
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8418505/
https://www.ncbi.nlm.nih.gov/pubmed/34288108
http://dx.doi.org/10.1002/jcla.23904
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