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Evaluation of serum MUC5AC in combination with CA19-9 for the diagnosis of pancreatic cancer
BACKGROUND: Pancreatic cancer (PC) is a highly aggressive tumor with a poor prognosis that lacks specific diagnostic markers. Mucin 5AC (MUC5AC) is a member of the mucin family, a heterogeneous group of high molecular weight, heavily glycosylated proteins that could be either membrane-bound or secre...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006398/ https://www.ncbi.nlm.nih.gov/pubmed/32028958 http://dx.doi.org/10.1186/s12957-020-1809-z |
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author | Zhang, Jiayu Wang, Yue Zhao, Tiancheng Li, Yezhou Tian, Leilei Zhao, Jinming Zhang, Jingxin |
author_facet | Zhang, Jiayu Wang, Yue Zhao, Tiancheng Li, Yezhou Tian, Leilei Zhao, Jinming Zhang, Jingxin |
author_sort | Zhang, Jiayu |
collection | PubMed |
description | BACKGROUND: Pancreatic cancer (PC) is a highly aggressive tumor with a poor prognosis that lacks specific diagnostic markers. Mucin 5AC (MUC5AC) is a member of the mucin family, a heterogeneous group of high molecular weight, heavily glycosylated proteins that could be either membrane-bound or secreted. This multi-central study is to evaluate the performance of serum MUC5AC in combination with carbohydrate antigen 19-9 (CA19-9) for the diagnosis of PC in Asian. METHODS: Sixty-one patients with PC (comprised of early pancreatic cancer [n = 30] and late pancreatic cancer [n = 31] patients), 29 benign control, 35 choledocholithiasis, 25 chronic pancreatitis, and 34 healthy controls, were recruited from two hospitals. Serum levels of MUC5AC were evaluated by commercial ELISA kits. CA19-9 was measured by chemiluminescence immunoassay. The cutoff value of MUC5AC was determined based on optimal sensitivity and specificity. RESULTS: Serum MUC5AC in patients with PC (210.1 [100.5–423.8] ng/mL) presented higher levels than those in controls. The combined biomarker panel (MUC5AC and CA19-9) presented better performance and improved specificity to differentiate PC from controls (AUC 0.894; 95% CI (0.844–0.943), sensitivity 0.738, specificity 0.886) than CA19-9 (p = 0.043) or MUC5AC alone (p = 0.010); however, the latter two had no difference (p = 0.824). CONCLUSIONS: Serum MUC5AC is a potential biomarker for PC. The combination with CA19-9 presents improved specificity and better performance. |
format | Online Article Text |
id | pubmed-7006398 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-70063982020-02-13 Evaluation of serum MUC5AC in combination with CA19-9 for the diagnosis of pancreatic cancer Zhang, Jiayu Wang, Yue Zhao, Tiancheng Li, Yezhou Tian, Leilei Zhao, Jinming Zhang, Jingxin World J Surg Oncol Research BACKGROUND: Pancreatic cancer (PC) is a highly aggressive tumor with a poor prognosis that lacks specific diagnostic markers. Mucin 5AC (MUC5AC) is a member of the mucin family, a heterogeneous group of high molecular weight, heavily glycosylated proteins that could be either membrane-bound or secreted. This multi-central study is to evaluate the performance of serum MUC5AC in combination with carbohydrate antigen 19-9 (CA19-9) for the diagnosis of PC in Asian. METHODS: Sixty-one patients with PC (comprised of early pancreatic cancer [n = 30] and late pancreatic cancer [n = 31] patients), 29 benign control, 35 choledocholithiasis, 25 chronic pancreatitis, and 34 healthy controls, were recruited from two hospitals. Serum levels of MUC5AC were evaluated by commercial ELISA kits. CA19-9 was measured by chemiluminescence immunoassay. The cutoff value of MUC5AC was determined based on optimal sensitivity and specificity. RESULTS: Serum MUC5AC in patients with PC (210.1 [100.5–423.8] ng/mL) presented higher levels than those in controls. The combined biomarker panel (MUC5AC and CA19-9) presented better performance and improved specificity to differentiate PC from controls (AUC 0.894; 95% CI (0.844–0.943), sensitivity 0.738, specificity 0.886) than CA19-9 (p = 0.043) or MUC5AC alone (p = 0.010); however, the latter two had no difference (p = 0.824). CONCLUSIONS: Serum MUC5AC is a potential biomarker for PC. The combination with CA19-9 presents improved specificity and better performance. BioMed Central 2020-02-07 /pmc/articles/PMC7006398/ /pubmed/32028958 http://dx.doi.org/10.1186/s12957-020-1809-z Text en © The Author(s). 2020 Open Access This 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 Zhang, Jiayu Wang, Yue Zhao, Tiancheng Li, Yezhou Tian, Leilei Zhao, Jinming Zhang, Jingxin Evaluation of serum MUC5AC in combination with CA19-9 for the diagnosis of pancreatic cancer |
title | Evaluation of serum MUC5AC in combination with CA19-9 for the diagnosis of pancreatic cancer |
title_full | Evaluation of serum MUC5AC in combination with CA19-9 for the diagnosis of pancreatic cancer |
title_fullStr | Evaluation of serum MUC5AC in combination with CA19-9 for the diagnosis of pancreatic cancer |
title_full_unstemmed | Evaluation of serum MUC5AC in combination with CA19-9 for the diagnosis of pancreatic cancer |
title_short | Evaluation of serum MUC5AC in combination with CA19-9 for the diagnosis of pancreatic cancer |
title_sort | evaluation of serum muc5ac in combination with ca19-9 for the diagnosis of pancreatic cancer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006398/ https://www.ncbi.nlm.nih.gov/pubmed/32028958 http://dx.doi.org/10.1186/s12957-020-1809-z |
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