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Application of serum SELDI proteomic patterns in diagnosis of lung cancer

BACKGROUND: Currently, no satisfactory biomarkers are available to screen for lung cancer. Surface-Enhanced Laser Desorption/ionization Time-of- Flight Mass Spectrometry ProteinChip system (SELDI-TOF-MS) is one of the currently used techniques to identify biomarkers for cancers. The aim of this stud...

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Autores principales: Yang, Shuan-ying, Xiao, Xue-yuan, Zhang, Wang-gang, Zhang, Li-juan, Zhang, Wei, Zhou, Bin, Chen, Guoan, He, Da-cheng
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1183195/
https://www.ncbi.nlm.nih.gov/pubmed/16029516
http://dx.doi.org/10.1186/1471-2407-5-83
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author Yang, Shuan-ying
Xiao, Xue-yuan
Zhang, Wang-gang
Zhang, Li-juan
Zhang, Wei
Zhou, Bin
Chen, Guoan
He, Da-cheng
author_facet Yang, Shuan-ying
Xiao, Xue-yuan
Zhang, Wang-gang
Zhang, Li-juan
Zhang, Wei
Zhou, Bin
Chen, Guoan
He, Da-cheng
author_sort Yang, Shuan-ying
collection PubMed
description BACKGROUND: Currently, no satisfactory biomarkers are available to screen for lung cancer. Surface-Enhanced Laser Desorption/ionization Time-of- Flight Mass Spectrometry ProteinChip system (SELDI-TOF-MS) is one of the currently used techniques to identify biomarkers for cancers. The aim of this study is to explore the application of serum SELDI proteomic patterns to distinguish lung cancer patients from healthy individuals. METHODS: A total of 208 serum samples, including 158 lung cancer patients and 50 healthy individuals, were randomly divided into a training set (including 11 sera from patients with stages I/II lung cancer, 63 from patients with stages III/IV lung cancer and 20 from healthy controls) and a blinded test set (including 43 sera from patients with stages I/II lung cancer, 41 from patients with stages III/IV lung cancer and 30 from healthy controls). All samples were analyzed by SELDI technology. The spectra were generated on weak cation exchange (WCX2) chips, and protein peaks clustering and classification analyses were made using Ciphergen Biomarker Wizard and Biomarker Pattern software, respectively. We additionally determined Cyfra21-1 and NSE in the 208 serum samples included in this study using an electrochemiluminescent immunoassay. RESULTS: Five protein peaks at 11493, 6429, 8245, 5335 and 2538 Da were automatically chosen as a biomarker pattern in the training set. When the SELDI marker pattern was tested with the blinded test set, it yielded a sensitivity of 86.9%, a specificity of 80.0% and a positive predictive value of 92.4%. The sensitivities provided by Cyfra21-1 and NSE used individually or in combination were significantly lower than that of the SELDI marker pattern (P < 0.005 or 0.05, respectively). Based on the results of the test set, we found that the SELDI marker pattern showed a sensitivity of 91.4% in the detection of non-small cell lung cancers (NSCLC), which was significantly higher than that in the detection of small cell lung cancers (P < 0.05); The pattern also had a sensitivity of 79.1% in the detection of lung cancers in stages I/II. CONCLUSION: These results suggest that serum SELDI protein profiling can distinguish lung cancer patients, especially NSCLC patients, from normal subjects with relatively high sensitivity and specificity, and the SELDI-TOF-MS is a potential tool for the screening of lung cancer.
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spelling pubmed-11831952005-08-06 Application of serum SELDI proteomic patterns in diagnosis of lung cancer Yang, Shuan-ying Xiao, Xue-yuan Zhang, Wang-gang Zhang, Li-juan Zhang, Wei Zhou, Bin Chen, Guoan He, Da-cheng BMC Cancer Research Article BACKGROUND: Currently, no satisfactory biomarkers are available to screen for lung cancer. Surface-Enhanced Laser Desorption/ionization Time-of- Flight Mass Spectrometry ProteinChip system (SELDI-TOF-MS) is one of the currently used techniques to identify biomarkers for cancers. The aim of this study is to explore the application of serum SELDI proteomic patterns to distinguish lung cancer patients from healthy individuals. METHODS: A total of 208 serum samples, including 158 lung cancer patients and 50 healthy individuals, were randomly divided into a training set (including 11 sera from patients with stages I/II lung cancer, 63 from patients with stages III/IV lung cancer and 20 from healthy controls) and a blinded test set (including 43 sera from patients with stages I/II lung cancer, 41 from patients with stages III/IV lung cancer and 30 from healthy controls). All samples were analyzed by SELDI technology. The spectra were generated on weak cation exchange (WCX2) chips, and protein peaks clustering and classification analyses were made using Ciphergen Biomarker Wizard and Biomarker Pattern software, respectively. We additionally determined Cyfra21-1 and NSE in the 208 serum samples included in this study using an electrochemiluminescent immunoassay. RESULTS: Five protein peaks at 11493, 6429, 8245, 5335 and 2538 Da were automatically chosen as a biomarker pattern in the training set. When the SELDI marker pattern was tested with the blinded test set, it yielded a sensitivity of 86.9%, a specificity of 80.0% and a positive predictive value of 92.4%. The sensitivities provided by Cyfra21-1 and NSE used individually or in combination were significantly lower than that of the SELDI marker pattern (P < 0.005 or 0.05, respectively). Based on the results of the test set, we found that the SELDI marker pattern showed a sensitivity of 91.4% in the detection of non-small cell lung cancers (NSCLC), which was significantly higher than that in the detection of small cell lung cancers (P < 0.05); The pattern also had a sensitivity of 79.1% in the detection of lung cancers in stages I/II. CONCLUSION: These results suggest that serum SELDI protein profiling can distinguish lung cancer patients, especially NSCLC patients, from normal subjects with relatively high sensitivity and specificity, and the SELDI-TOF-MS is a potential tool for the screening of lung cancer. BioMed Central 2005-07-20 /pmc/articles/PMC1183195/ /pubmed/16029516 http://dx.doi.org/10.1186/1471-2407-5-83 Text en Copyright © 2005 Yang et al; licensee BioMed Central Ltd.
spellingShingle Research Article
Yang, Shuan-ying
Xiao, Xue-yuan
Zhang, Wang-gang
Zhang, Li-juan
Zhang, Wei
Zhou, Bin
Chen, Guoan
He, Da-cheng
Application of serum SELDI proteomic patterns in diagnosis of lung cancer
title Application of serum SELDI proteomic patterns in diagnosis of lung cancer
title_full Application of serum SELDI proteomic patterns in diagnosis of lung cancer
title_fullStr Application of serum SELDI proteomic patterns in diagnosis of lung cancer
title_full_unstemmed Application of serum SELDI proteomic patterns in diagnosis of lung cancer
title_short Application of serum SELDI proteomic patterns in diagnosis of lung cancer
title_sort application of serum seldi proteomic patterns in diagnosis of lung cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1183195/
https://www.ncbi.nlm.nih.gov/pubmed/16029516
http://dx.doi.org/10.1186/1471-2407-5-83
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