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Proteomic analysis of non-small cell lung cancer tissue interstitial fluids
BACKGROUND: Non-small cell lung cancer (NSCLC) accounts for more than 80% of all lung cancers, and reliable biomarkers are desirable. The present investigation assesses our ability to identify tumor relevant proteins from NSCLC tissue interstitial fluid (TIF). METHODS: Paired TIF was collected from...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751644/ https://www.ncbi.nlm.nih.gov/pubmed/23914992 http://dx.doi.org/10.1186/1477-7819-11-173 |
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author | Li, Shaomin Wang, Rui Zhang, Mingxin Wang, Lina Cheng, Shaoli |
author_facet | Li, Shaomin Wang, Rui Zhang, Mingxin Wang, Lina Cheng, Shaoli |
author_sort | Li, Shaomin |
collection | PubMed |
description | BACKGROUND: Non-small cell lung cancer (NSCLC) accounts for more than 80% of all lung cancers, and reliable biomarkers are desirable. The present investigation assesses our ability to identify tumor relevant proteins from NSCLC tissue interstitial fluid (TIF). METHODS: Paired TIF was collected from three NSCLC patients at the time of surgery, and resolved by two-dimensional gel electrophoresis and in-gel digestion for proteomic analysis. Differentially expressed spots were extracted from the two-dimensional gel and characterized by high-performance liquid chromatography-tandem mass spectrometry. Then, ELISA was used to verify the expression of peroxiredoxin 1 (PRDX1) in TIF of patients with NSCLC and benign lung disease. Finally, the relationship between expression of PRDX1 and clinicopathological features was determined. RESULTS: Comparative proteomic analysis showed 24 protein spots were differentially expressed with significant changes, including 11 upregulated proteins and 13 downregulated proteins. Of these, PRDX1 was selected for validation in TIF by Western blot and expression of PRDX1 was confirmed to be upregulated in tumor TIF. It was also demonstrated that PRDX1 was significantly elevated in 40 NSCLC patients with a mean level of 36.0 ng/mL compared to 6.26 ng/mL from 20 patients with benign lung disease. A significant correlation was found between the high level of PRDX1 expression and lymph node metastasis and tumor differentiation. CONCLUSIONS: PRDX1 might be correlated with lymph node metastasis and differentiation, and its elevated expression in TIF may be an adverse biomarker for patients with NSCLC. PRDX1 may be attributed to the malignant transformation of NSCLC, and attention should be paid to a possible target for therapy. |
format | Online Article Text |
id | pubmed-3751644 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-37516442013-08-24 Proteomic analysis of non-small cell lung cancer tissue interstitial fluids Li, Shaomin Wang, Rui Zhang, Mingxin Wang, Lina Cheng, Shaoli World J Surg Oncol Research BACKGROUND: Non-small cell lung cancer (NSCLC) accounts for more than 80% of all lung cancers, and reliable biomarkers are desirable. The present investigation assesses our ability to identify tumor relevant proteins from NSCLC tissue interstitial fluid (TIF). METHODS: Paired TIF was collected from three NSCLC patients at the time of surgery, and resolved by two-dimensional gel electrophoresis and in-gel digestion for proteomic analysis. Differentially expressed spots were extracted from the two-dimensional gel and characterized by high-performance liquid chromatography-tandem mass spectrometry. Then, ELISA was used to verify the expression of peroxiredoxin 1 (PRDX1) in TIF of patients with NSCLC and benign lung disease. Finally, the relationship between expression of PRDX1 and clinicopathological features was determined. RESULTS: Comparative proteomic analysis showed 24 protein spots were differentially expressed with significant changes, including 11 upregulated proteins and 13 downregulated proteins. Of these, PRDX1 was selected for validation in TIF by Western blot and expression of PRDX1 was confirmed to be upregulated in tumor TIF. It was also demonstrated that PRDX1 was significantly elevated in 40 NSCLC patients with a mean level of 36.0 ng/mL compared to 6.26 ng/mL from 20 patients with benign lung disease. A significant correlation was found between the high level of PRDX1 expression and lymph node metastasis and tumor differentiation. CONCLUSIONS: PRDX1 might be correlated with lymph node metastasis and differentiation, and its elevated expression in TIF may be an adverse biomarker for patients with NSCLC. PRDX1 may be attributed to the malignant transformation of NSCLC, and attention should be paid to a possible target for therapy. BioMed Central 2013-08-05 /pmc/articles/PMC3751644/ /pubmed/23914992 http://dx.doi.org/10.1186/1477-7819-11-173 Text en Copyright ©2013 Li 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 Li, Shaomin Wang, Rui Zhang, Mingxin Wang, Lina Cheng, Shaoli Proteomic analysis of non-small cell lung cancer tissue interstitial fluids |
title | Proteomic analysis of non-small cell lung cancer tissue interstitial fluids |
title_full | Proteomic analysis of non-small cell lung cancer tissue interstitial fluids |
title_fullStr | Proteomic analysis of non-small cell lung cancer tissue interstitial fluids |
title_full_unstemmed | Proteomic analysis of non-small cell lung cancer tissue interstitial fluids |
title_short | Proteomic analysis of non-small cell lung cancer tissue interstitial fluids |
title_sort | proteomic analysis of non-small cell lung cancer tissue interstitial fluids |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751644/ https://www.ncbi.nlm.nih.gov/pubmed/23914992 http://dx.doi.org/10.1186/1477-7819-11-173 |
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