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Correlation study between serum neuro-specific enolase and gastric and colorectal cancers
This study investigated the diagnostic value of preoperative serum neuro-specific enolase (NSE) in gastric cancer (GC) and colorectal cancer (CRC), and the diagnostic viability of combined serum NSE, carcinoembryonic antigen (CEA), cancer antigen (CA)19-9, and CA242. Patients with GC and CRC, and a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7440092/ https://www.ncbi.nlm.nih.gov/pubmed/32311993 http://dx.doi.org/10.1097/MD.0000000000019796 |
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author | Luo, Hai Shen, Kexin Sun, Hongyan Li, Ruiqi Wang, Zeming Xie, Zhongshi |
author_facet | Luo, Hai Shen, Kexin Sun, Hongyan Li, Ruiqi Wang, Zeming Xie, Zhongshi |
author_sort | Luo, Hai |
collection | PubMed |
description | This study investigated the diagnostic value of preoperative serum neuro-specific enolase (NSE) in gastric cancer (GC) and colorectal cancer (CRC), and the diagnostic viability of combined serum NSE, carcinoembryonic antigen (CEA), cancer antigen (CA)19-9, and CA242. Patients with GC and CRC, and a healthy control group (n = 666 and 266, respectively) were compared with regard to NSE, CEA, CA19-9, and CA242 serum levels. NSE was analyzed for associations with clinicopathological parameters. To estimate the diagnostic potential of NSE, a receiver operating characteristic curve was constructed and the area under the curve (AUCs) was calculated for different patient subgroups. The median serum NSE level of the tumor group (20.925 ng/mL) was significantly higher than that of the control (15.190 ng/mL). Serum NSE was associated with pathological tumor-node-metastasis staging, lymph node metastasis, distant metastasis, vascular invasion, and nerve infiltration. The area under the receiver operating characteristic curve (AUC) for NSE in GC and CRC (0.769) was higher than for the other 3 markers (0.571–0.680). The AUC of the combined markers was higher than for any of the markers individually (0.778–0.810). The AUC for NSE alone suggests it may be an independent tumor marker, and useful for diagnosis of GC and CRC. However, the AUC for combined NSE, CEA, CA19-9, and CA242 was higher and thus potentially more diagnostic value. |
format | Online Article Text |
id | pubmed-7440092 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-74400922020-09-04 Correlation study between serum neuro-specific enolase and gastric and colorectal cancers Luo, Hai Shen, Kexin Sun, Hongyan Li, Ruiqi Wang, Zeming Xie, Zhongshi Medicine (Baltimore) 5700 This study investigated the diagnostic value of preoperative serum neuro-specific enolase (NSE) in gastric cancer (GC) and colorectal cancer (CRC), and the diagnostic viability of combined serum NSE, carcinoembryonic antigen (CEA), cancer antigen (CA)19-9, and CA242. Patients with GC and CRC, and a healthy control group (n = 666 and 266, respectively) were compared with regard to NSE, CEA, CA19-9, and CA242 serum levels. NSE was analyzed for associations with clinicopathological parameters. To estimate the diagnostic potential of NSE, a receiver operating characteristic curve was constructed and the area under the curve (AUCs) was calculated for different patient subgroups. The median serum NSE level of the tumor group (20.925 ng/mL) was significantly higher than that of the control (15.190 ng/mL). Serum NSE was associated with pathological tumor-node-metastasis staging, lymph node metastasis, distant metastasis, vascular invasion, and nerve infiltration. The area under the receiver operating characteristic curve (AUC) for NSE in GC and CRC (0.769) was higher than for the other 3 markers (0.571–0.680). The AUC of the combined markers was higher than for any of the markers individually (0.778–0.810). The AUC for NSE alone suggests it may be an independent tumor marker, and useful for diagnosis of GC and CRC. However, the AUC for combined NSE, CEA, CA19-9, and CA242 was higher and thus potentially more diagnostic value. Wolters Kluwer Health 2020-04-17 /pmc/articles/PMC7440092/ /pubmed/32311993 http://dx.doi.org/10.1097/MD.0000000000019796 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | 5700 Luo, Hai Shen, Kexin Sun, Hongyan Li, Ruiqi Wang, Zeming Xie, Zhongshi Correlation study between serum neuro-specific enolase and gastric and colorectal cancers |
title | Correlation study between serum neuro-specific enolase and gastric and colorectal cancers |
title_full | Correlation study between serum neuro-specific enolase and gastric and colorectal cancers |
title_fullStr | Correlation study between serum neuro-specific enolase and gastric and colorectal cancers |
title_full_unstemmed | Correlation study between serum neuro-specific enolase and gastric and colorectal cancers |
title_short | Correlation study between serum neuro-specific enolase and gastric and colorectal cancers |
title_sort | correlation study between serum neuro-specific enolase and gastric and colorectal cancers |
topic | 5700 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7440092/ https://www.ncbi.nlm.nih.gov/pubmed/32311993 http://dx.doi.org/10.1097/MD.0000000000019796 |
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