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Serum biomarker panels for the diagnosis of gastric cancer

Gastric cancer is a leading cause of mortality due to neoplastic disease. Although early detection of gastric cancers can decrease the mortality rate, it remains a diagnostic challenge because of the lack of effective biomarkers. In this study, fifteen gastric cancer patients and ten healthy subject...

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Autores principales: Wu, Dan, Zhang, Pinglu, Ma, Ji, Xu, Jinbo, Yang, Li, Xu, Weidan, Que, Haifeng, Chen, Meifen, Xu, Hongtao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488129/
https://www.ncbi.nlm.nih.gov/pubmed/30873760
http://dx.doi.org/10.1002/cam4.2055
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author Wu, Dan
Zhang, Pinglu
Ma, Ji
Xu, Jinbo
Yang, Li
Xu, Weidan
Que, Haifeng
Chen, Meifen
Xu, Hongtao
author_facet Wu, Dan
Zhang, Pinglu
Ma, Ji
Xu, Jinbo
Yang, Li
Xu, Weidan
Que, Haifeng
Chen, Meifen
Xu, Hongtao
author_sort Wu, Dan
collection PubMed
description Gastric cancer is a leading cause of mortality due to neoplastic disease. Although early detection of gastric cancers can decrease the mortality rate, it remains a diagnostic challenge because of the lack of effective biomarkers. In this study, fifteen gastric cancer patients and ten healthy subjects were recruited to assess novel serum biomarkers for gastric cancer using antibody microarray technology. ELISA was utilized to validate the antibody array results. As a result, compared to the controls, eleven cytokines were found to be significantly increased in gastric cancer, including interferon gamma receptor 1 (IFNGR1), neurogenic locus notch homolog protein 3 (Notch‐3), tumor necrosis factor receptor superfamily member 19L (TNFRSF19L), growth hormone receptor (GHR), signaling lymphocytic activation molecule family 8 (SLAMF8), folate receptor beta (FR‐beta), integrin alpha 5, galectin‐8, erythropoietin‐producing hepatocellular A1 (EphA1), epiregulin, and fibroblast growth factor 12 (FGF‐12) with P < 0.05. ELISA validation supported the results of the antibody array. More importantly, most of these eleven cytokines, including IFNGR1, TNFRSF19L, GHR, SLAMF8, FR‐beta, and integrin alpha 5 were discovered to be elevated in gastric cancer serum samples for the first time in this study, suggesting that these proteins may serve as novel biomarkers for the early diagnosis and prognosis determination of gastric cancer.
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spelling pubmed-64881292019-05-23 Serum biomarker panels for the diagnosis of gastric cancer Wu, Dan Zhang, Pinglu Ma, Ji Xu, Jinbo Yang, Li Xu, Weidan Que, Haifeng Chen, Meifen Xu, Hongtao Cancer Med Clinical Cancer Research Gastric cancer is a leading cause of mortality due to neoplastic disease. Although early detection of gastric cancers can decrease the mortality rate, it remains a diagnostic challenge because of the lack of effective biomarkers. In this study, fifteen gastric cancer patients and ten healthy subjects were recruited to assess novel serum biomarkers for gastric cancer using antibody microarray technology. ELISA was utilized to validate the antibody array results. As a result, compared to the controls, eleven cytokines were found to be significantly increased in gastric cancer, including interferon gamma receptor 1 (IFNGR1), neurogenic locus notch homolog protein 3 (Notch‐3), tumor necrosis factor receptor superfamily member 19L (TNFRSF19L), growth hormone receptor (GHR), signaling lymphocytic activation molecule family 8 (SLAMF8), folate receptor beta (FR‐beta), integrin alpha 5, galectin‐8, erythropoietin‐producing hepatocellular A1 (EphA1), epiregulin, and fibroblast growth factor 12 (FGF‐12) with P < 0.05. ELISA validation supported the results of the antibody array. More importantly, most of these eleven cytokines, including IFNGR1, TNFRSF19L, GHR, SLAMF8, FR‐beta, and integrin alpha 5 were discovered to be elevated in gastric cancer serum samples for the first time in this study, suggesting that these proteins may serve as novel biomarkers for the early diagnosis and prognosis determination of gastric cancer. John Wiley and Sons Inc. 2019-03-14 /pmc/articles/PMC6488129/ /pubmed/30873760 http://dx.doi.org/10.1002/cam4.2055 Text en © 2019 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Wu, Dan
Zhang, Pinglu
Ma, Ji
Xu, Jinbo
Yang, Li
Xu, Weidan
Que, Haifeng
Chen, Meifen
Xu, Hongtao
Serum biomarker panels for the diagnosis of gastric cancer
title Serum biomarker panels for the diagnosis of gastric cancer
title_full Serum biomarker panels for the diagnosis of gastric cancer
title_fullStr Serum biomarker panels for the diagnosis of gastric cancer
title_full_unstemmed Serum biomarker panels for the diagnosis of gastric cancer
title_short Serum biomarker panels for the diagnosis of gastric cancer
title_sort serum biomarker panels for the diagnosis of gastric cancer
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488129/
https://www.ncbi.nlm.nih.gov/pubmed/30873760
http://dx.doi.org/10.1002/cam4.2055
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