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Mining novel biomarkers for prognosis of gastric cancer with serum proteomics

BACKGROUND: Although gastric caner (GC) remains the second cause of cancer-related death, useful biomarkers for prognosis are still unavailable. We present here the attempt of mining novel biomarkers for GC prognosis by using serum proteomics. METHODS: Sera from 43 GC patients and 41 controls with g...

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Autores principales: Qiu, Fu-Ming, Yu, Jie-Kai, Chen, Yi-Ding, Jin, Qi-Feng, Sui, Mei-Hua, Huang, Jian
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2753349/
https://www.ncbi.nlm.nih.gov/pubmed/19740432
http://dx.doi.org/10.1186/1756-9966-28-126
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author Qiu, Fu-Ming
Yu, Jie-Kai
Chen, Yi-Ding
Jin, Qi-Feng
Sui, Mei-Hua
Huang, Jian
author_facet Qiu, Fu-Ming
Yu, Jie-Kai
Chen, Yi-Ding
Jin, Qi-Feng
Sui, Mei-Hua
Huang, Jian
author_sort Qiu, Fu-Ming
collection PubMed
description BACKGROUND: Although gastric caner (GC) remains the second cause of cancer-related death, useful biomarkers for prognosis are still unavailable. We present here the attempt of mining novel biomarkers for GC prognosis by using serum proteomics. METHODS: Sera from 43 GC patients and 41 controls with gastritis as Group 1 and 11 GC patients as Group 2 was successively detected by Surface Enhanced Laser Desorption/ionization Time of Flight Mass Spectrometry (SELDI-TOF-MS) with Q10 chip. Peaks were acquired by Ciphergen ProteinChip Software 3.2.0 and analyzed by Zhejiang University-ProteinChip Data Analysis System (ZJU-PDAS). CEA level were evaluated by chemiluminescence immunoassay. RESULTS: After median follow-up periods of 33 months, Group 1 with 4 GC patients lost was divided into 20 good-prognosis GC patients (overall survival more than 24 months) and 19 poor-prognosis GC patients (no more than 24 months). The established prognosis pattern consisted of 5 novel prognosis biomarkers with 84.2% sensitivity and 85.0% specificity, which were significantly higher than those of carcinoembryonic antigen (CEA) and TNM stage. We also tested prognosis pattern blindly in Group 2 with 66.7% sensitivity and 80.0% specificity. Moreover, we found that 4474-Da peak elevated significantly in GC and was associated with advanced stage (III+IV) and short survival (p < 0.03). CONCLUSION: We have identified a number of novel biomarkers for prognosis prediction of GC by using SELDI-TOF-MS combined with sophisticated bioinformatics. Particularly, elevated expression of 4474-Da peak showed very promising to be developed into a novel biomarker associated with biologically aggressive features of GC.
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spelling pubmed-27533492009-09-29 Mining novel biomarkers for prognosis of gastric cancer with serum proteomics Qiu, Fu-Ming Yu, Jie-Kai Chen, Yi-Ding Jin, Qi-Feng Sui, Mei-Hua Huang, Jian J Exp Clin Cancer Res Research BACKGROUND: Although gastric caner (GC) remains the second cause of cancer-related death, useful biomarkers for prognosis are still unavailable. We present here the attempt of mining novel biomarkers for GC prognosis by using serum proteomics. METHODS: Sera from 43 GC patients and 41 controls with gastritis as Group 1 and 11 GC patients as Group 2 was successively detected by Surface Enhanced Laser Desorption/ionization Time of Flight Mass Spectrometry (SELDI-TOF-MS) with Q10 chip. Peaks were acquired by Ciphergen ProteinChip Software 3.2.0 and analyzed by Zhejiang University-ProteinChip Data Analysis System (ZJU-PDAS). CEA level were evaluated by chemiluminescence immunoassay. RESULTS: After median follow-up periods of 33 months, Group 1 with 4 GC patients lost was divided into 20 good-prognosis GC patients (overall survival more than 24 months) and 19 poor-prognosis GC patients (no more than 24 months). The established prognosis pattern consisted of 5 novel prognosis biomarkers with 84.2% sensitivity and 85.0% specificity, which were significantly higher than those of carcinoembryonic antigen (CEA) and TNM stage. We also tested prognosis pattern blindly in Group 2 with 66.7% sensitivity and 80.0% specificity. Moreover, we found that 4474-Da peak elevated significantly in GC and was associated with advanced stage (III+IV) and short survival (p < 0.03). CONCLUSION: We have identified a number of novel biomarkers for prognosis prediction of GC by using SELDI-TOF-MS combined with sophisticated bioinformatics. Particularly, elevated expression of 4474-Da peak showed very promising to be developed into a novel biomarker associated with biologically aggressive features of GC. BioMed Central 2009-09-09 /pmc/articles/PMC2753349/ /pubmed/19740432 http://dx.doi.org/10.1186/1756-9966-28-126 Text en Copyright © 2009 Qiu et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Qiu, Fu-Ming
Yu, Jie-Kai
Chen, Yi-Ding
Jin, Qi-Feng
Sui, Mei-Hua
Huang, Jian
Mining novel biomarkers for prognosis of gastric cancer with serum proteomics
title Mining novel biomarkers for prognosis of gastric cancer with serum proteomics
title_full Mining novel biomarkers for prognosis of gastric cancer with serum proteomics
title_fullStr Mining novel biomarkers for prognosis of gastric cancer with serum proteomics
title_full_unstemmed Mining novel biomarkers for prognosis of gastric cancer with serum proteomics
title_short Mining novel biomarkers for prognosis of gastric cancer with serum proteomics
title_sort mining novel biomarkers for prognosis of gastric cancer with serum proteomics
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2753349/
https://www.ncbi.nlm.nih.gov/pubmed/19740432
http://dx.doi.org/10.1186/1756-9966-28-126
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