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The matrix metalloproteinase and insulin-like growth factor system in oral cancer – a prospective clinical study
AIM: The absence of reliable single serum biomarkers for oral premalignant lesion (OPL) and oral squamous cell carcinoma (OSCC) limits early diagnosis, monitoring of advanced disease, and prediction of prognosis. METHODS: In this prospective study, serum levels of matrix metalloproteinase (MMP)-2, M...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5661464/ https://www.ncbi.nlm.nih.gov/pubmed/29123408 http://dx.doi.org/10.2147/OTT.S149231 |
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author | Schiegnitz, Eik Kämmerer, Peer W Schön, Holger Gülle, Christoph Berres, Manfred Sagheb, Keyvan Al-Nawas, Bilal |
author_facet | Schiegnitz, Eik Kämmerer, Peer W Schön, Holger Gülle, Christoph Berres, Manfred Sagheb, Keyvan Al-Nawas, Bilal |
author_sort | Schiegnitz, Eik |
collection | PubMed |
description | AIM: The absence of reliable single serum biomarkers for oral premalignant lesion (OPL) and oral squamous cell carcinoma (OSCC) limits early diagnosis, monitoring of advanced disease, and prediction of prognosis. METHODS: In this prospective study, serum levels of matrix metalloproteinase (MMP)-2, MMP-3, MMP-13, insulin-like growth factor (IGF)-1, and IGF-binding protein (IGFBP)-3 were measured in 81 untreated OSCC patients, 49 healthy subjects, and 75 individuals with OPLs, and correlated with clinicopathological parameters. RESULTS: Serum levels of MMP-3 were significantly higher in OSCC patients compared to healthy subjects (p=0.004). Mean IGF-1 and IGFBP-3 levels in OSCC patients were significantly lower in healthy subjects (p=0.001 and p<0.001). OSCC patients with an IGF-1 serum value <130 ng/mL (median) showed a significantly lower survival rate compared to ≥130 ng/mL (p=0.049). Combined use of IGF-1 (<130 ng/mL) and IGFBP-3 (<3.1 μg/mL) resulted in a significantly lower 12-month cumulative survival compared to the complementary set (78.5% vs 93.8%; p=0.031). There was a significantly positive correlation between IGF-1 and IGFBP-3 serum values (r(s) =0.625, p<0.001). CONCLUSION: This study shows that IGF-1 and IGFBP-3 have a vital role in the pathogenesis of OSCC and indicates for the first time that IGF-1 and IGFBP-3 in combination may be applied as potential tools for prognosis of OSCC. |
format | Online Article Text |
id | pubmed-5661464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-56614642017-11-09 The matrix metalloproteinase and insulin-like growth factor system in oral cancer – a prospective clinical study Schiegnitz, Eik Kämmerer, Peer W Schön, Holger Gülle, Christoph Berres, Manfred Sagheb, Keyvan Al-Nawas, Bilal Onco Targets Ther Original Research AIM: The absence of reliable single serum biomarkers for oral premalignant lesion (OPL) and oral squamous cell carcinoma (OSCC) limits early diagnosis, monitoring of advanced disease, and prediction of prognosis. METHODS: In this prospective study, serum levels of matrix metalloproteinase (MMP)-2, MMP-3, MMP-13, insulin-like growth factor (IGF)-1, and IGF-binding protein (IGFBP)-3 were measured in 81 untreated OSCC patients, 49 healthy subjects, and 75 individuals with OPLs, and correlated with clinicopathological parameters. RESULTS: Serum levels of MMP-3 were significantly higher in OSCC patients compared to healthy subjects (p=0.004). Mean IGF-1 and IGFBP-3 levels in OSCC patients were significantly lower in healthy subjects (p=0.001 and p<0.001). OSCC patients with an IGF-1 serum value <130 ng/mL (median) showed a significantly lower survival rate compared to ≥130 ng/mL (p=0.049). Combined use of IGF-1 (<130 ng/mL) and IGFBP-3 (<3.1 μg/mL) resulted in a significantly lower 12-month cumulative survival compared to the complementary set (78.5% vs 93.8%; p=0.031). There was a significantly positive correlation between IGF-1 and IGFBP-3 serum values (r(s) =0.625, p<0.001). CONCLUSION: This study shows that IGF-1 and IGFBP-3 have a vital role in the pathogenesis of OSCC and indicates for the first time that IGF-1 and IGFBP-3 in combination may be applied as potential tools for prognosis of OSCC. Dove Medical Press 2017-10-24 /pmc/articles/PMC5661464/ /pubmed/29123408 http://dx.doi.org/10.2147/OTT.S149231 Text en © 2017 Schiegnitz et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Schiegnitz, Eik Kämmerer, Peer W Schön, Holger Gülle, Christoph Berres, Manfred Sagheb, Keyvan Al-Nawas, Bilal The matrix metalloproteinase and insulin-like growth factor system in oral cancer – a prospective clinical study |
title | The matrix metalloproteinase and insulin-like growth factor system in oral cancer – a prospective clinical study |
title_full | The matrix metalloproteinase and insulin-like growth factor system in oral cancer – a prospective clinical study |
title_fullStr | The matrix metalloproteinase and insulin-like growth factor system in oral cancer – a prospective clinical study |
title_full_unstemmed | The matrix metalloproteinase and insulin-like growth factor system in oral cancer – a prospective clinical study |
title_short | The matrix metalloproteinase and insulin-like growth factor system in oral cancer – a prospective clinical study |
title_sort | matrix metalloproteinase and insulin-like growth factor system in oral cancer – a prospective clinical study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5661464/ https://www.ncbi.nlm.nih.gov/pubmed/29123408 http://dx.doi.org/10.2147/OTT.S149231 |
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