Cargando…

Identification of biomarkers for lymph node metastasis in early-stage cervical cancer by tissue-based proteomics

BACKGROUND: Pelvic lymph node metastasis (PLNM) is the key to determining the treatment and prognosis of early-stage cervical cancer (CC, I–IIst). The aim of this study was to identify biomarkers for PLNM of CC, I–IIst. METHODS: Two-dimensional fluorescence difference gel electrophoresis and matrix-...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, W, Jia, H-L, Huang, J-M, Liang, Y-C, Tan, H, Geng, H-Z, Guo, L-Y, Yao, S-Z
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974096/
https://www.ncbi.nlm.nih.gov/pubmed/24569473
http://dx.doi.org/10.1038/bjc.2014.92
_version_ 1782479431072219136
author Wang, W
Jia, H-L
Huang, J-M
Liang, Y-C
Tan, H
Geng, H-Z
Guo, L-Y
Yao, S-Z
author_facet Wang, W
Jia, H-L
Huang, J-M
Liang, Y-C
Tan, H
Geng, H-Z
Guo, L-Y
Yao, S-Z
author_sort Wang, W
collection PubMed
description BACKGROUND: Pelvic lymph node metastasis (PLNM) is the key to determining the treatment and prognosis of early-stage cervical cancer (CC, I–IIst). The aim of this study was to identify biomarkers for PLNM of CC, I–IIst. METHODS: Two-dimensional fluorescence difference gel electrophoresis and matrix-assisted laser desorption/ionisation-time-of-flight mass spectrometry (MALDI-TOF/TOF MS) were used to identify differentially expressed proteins in primary CC, I–IIst tissue with (n=8) and without (n=10) PLNM. The expression levels of three differential proteins (FABP5, HspB1, and MnSOD) were validated using western blotting and immunohistochemistry. An independent cohort of 105 CC, I–IIst patients was analysed to assess the correlation of FABP5, HspB1, and MnSOD with clinicopathologic factors and clinical outcomes. RESULTS: Forty-one differential proteins were identified. Upregulation of FABP5, HspB1, and MnSOD in CC, I–IIst with PLNM was confirmed and was significantly correlated with PLNM. FABP5, HspB1, and MnSOD were significant predictors of PLNM in univariate analysis. FABP5, HspB1, and lymphovascular space invasion (LVSI) were independent predictors of PLNM in multivariate analysis. Survival curves indicated that CC, I–IIst patients with FABP5, HspB1, and MnSOD upregulation had poor prognosis. CONCLUSIONS: FABP5, HspB1, and MnSOD may be potential biomarkers for PLNM of CC, I–IIst and may have important roles in the pathogenesis of PLNM.
format Online
Article
Text
id pubmed-3974096
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-39740962015-04-01 Identification of biomarkers for lymph node metastasis in early-stage cervical cancer by tissue-based proteomics Wang, W Jia, H-L Huang, J-M Liang, Y-C Tan, H Geng, H-Z Guo, L-Y Yao, S-Z Br J Cancer Molecular Diagnostics BACKGROUND: Pelvic lymph node metastasis (PLNM) is the key to determining the treatment and prognosis of early-stage cervical cancer (CC, I–IIst). The aim of this study was to identify biomarkers for PLNM of CC, I–IIst. METHODS: Two-dimensional fluorescence difference gel electrophoresis and matrix-assisted laser desorption/ionisation-time-of-flight mass spectrometry (MALDI-TOF/TOF MS) were used to identify differentially expressed proteins in primary CC, I–IIst tissue with (n=8) and without (n=10) PLNM. The expression levels of three differential proteins (FABP5, HspB1, and MnSOD) were validated using western blotting and immunohistochemistry. An independent cohort of 105 CC, I–IIst patients was analysed to assess the correlation of FABP5, HspB1, and MnSOD with clinicopathologic factors and clinical outcomes. RESULTS: Forty-one differential proteins were identified. Upregulation of FABP5, HspB1, and MnSOD in CC, I–IIst with PLNM was confirmed and was significantly correlated with PLNM. FABP5, HspB1, and MnSOD were significant predictors of PLNM in univariate analysis. FABP5, HspB1, and lymphovascular space invasion (LVSI) were independent predictors of PLNM in multivariate analysis. Survival curves indicated that CC, I–IIst patients with FABP5, HspB1, and MnSOD upregulation had poor prognosis. CONCLUSIONS: FABP5, HspB1, and MnSOD may be potential biomarkers for PLNM of CC, I–IIst and may have important roles in the pathogenesis of PLNM. Nature Publishing Group 2014-04-01 2014-02-25 /pmc/articles/PMC3974096/ /pubmed/24569473 http://dx.doi.org/10.1038/bjc.2014.92 Text en Copyright © 2014 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Molecular Diagnostics
Wang, W
Jia, H-L
Huang, J-M
Liang, Y-C
Tan, H
Geng, H-Z
Guo, L-Y
Yao, S-Z
Identification of biomarkers for lymph node metastasis in early-stage cervical cancer by tissue-based proteomics
title Identification of biomarkers for lymph node metastasis in early-stage cervical cancer by tissue-based proteomics
title_full Identification of biomarkers for lymph node metastasis in early-stage cervical cancer by tissue-based proteomics
title_fullStr Identification of biomarkers for lymph node metastasis in early-stage cervical cancer by tissue-based proteomics
title_full_unstemmed Identification of biomarkers for lymph node metastasis in early-stage cervical cancer by tissue-based proteomics
title_short Identification of biomarkers for lymph node metastasis in early-stage cervical cancer by tissue-based proteomics
title_sort identification of biomarkers for lymph node metastasis in early-stage cervical cancer by tissue-based proteomics
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974096/
https://www.ncbi.nlm.nih.gov/pubmed/24569473
http://dx.doi.org/10.1038/bjc.2014.92
work_keys_str_mv AT wangw identificationofbiomarkersforlymphnodemetastasisinearlystagecervicalcancerbytissuebasedproteomics
AT jiahl identificationofbiomarkersforlymphnodemetastasisinearlystagecervicalcancerbytissuebasedproteomics
AT huangjm identificationofbiomarkersforlymphnodemetastasisinearlystagecervicalcancerbytissuebasedproteomics
AT liangyc identificationofbiomarkersforlymphnodemetastasisinearlystagecervicalcancerbytissuebasedproteomics
AT tanh identificationofbiomarkersforlymphnodemetastasisinearlystagecervicalcancerbytissuebasedproteomics
AT genghz identificationofbiomarkersforlymphnodemetastasisinearlystagecervicalcancerbytissuebasedproteomics
AT guoly identificationofbiomarkersforlymphnodemetastasisinearlystagecervicalcancerbytissuebasedproteomics
AT yaosz identificationofbiomarkersforlymphnodemetastasisinearlystagecervicalcancerbytissuebasedproteomics