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CD147 expression correlates with lymph node metastasis in T1-T2 squamous cell carcinoma of the tongue

Cervical lymph node metastasis causes a poor prognosis in cases of stage T1-T2 squamous cell carcinoma (SCC) of the tongue. Recent studies have reported that cluster of differentiation (CD)147, also known as extracellular matrix metalloproteinase inducer, contributes to tumor progression. The presen...

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Autores principales: Suzuki, Shinsuke, Honda, Kohei, Nanjo, Hiroshi, Iikawa, Nobuko, Tsuji, Tadahiro, Kawasaki, Yohei, Yamazaki, Kazuharu, Sato, Teruyuki, Saito, Hidekazu, Shiina, Kazuhiro, Ishikawa, Kazuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5649530/
https://www.ncbi.nlm.nih.gov/pubmed/29085466
http://dx.doi.org/10.3892/ol.2017.6808
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author Suzuki, Shinsuke
Honda, Kohei
Nanjo, Hiroshi
Iikawa, Nobuko
Tsuji, Tadahiro
Kawasaki, Yohei
Yamazaki, Kazuharu
Sato, Teruyuki
Saito, Hidekazu
Shiina, Kazuhiro
Ishikawa, Kazuo
author_facet Suzuki, Shinsuke
Honda, Kohei
Nanjo, Hiroshi
Iikawa, Nobuko
Tsuji, Tadahiro
Kawasaki, Yohei
Yamazaki, Kazuharu
Sato, Teruyuki
Saito, Hidekazu
Shiina, Kazuhiro
Ishikawa, Kazuo
author_sort Suzuki, Shinsuke
collection PubMed
description Cervical lymph node metastasis causes a poor prognosis in cases of stage T1-T2 squamous cell carcinoma (SCC) of the tongue. Recent studies have reported that cluster of differentiation (CD)147, also known as extracellular matrix metalloproteinase inducer, contributes to tumor progression. The present study evaluated the role of CD147 in the tumorigenesis of SCC of the tongue in vitro, as well as the association between CD147 expression and cervical lymph node metastasis in clinical samples of SCC of the tongue. Tongue SCC cell lines were used to evaluate in vitro tumorigenesis. In addition, 41 patients with clinical stage T1-T2 tongue SCC were assessed with a histopathological analysis. Univariate and multivariate analysis were performed to investigate the risk of cervical lymph node metastasis associated with histopathological findings. In the in vitro study, cell invasiveness was upregulated by S100 calcium-binding protein A9 (S100A9) stimulation and downregulated following CD147-blocking antibody treatment. The univariate and multivariate analyses identified CD147 expression in the invasive tumor front as an independent risk factor for metastasis. It was concluded that CD147 induces tongue carcinoma cell invasion through its interaction with S100A9. Thus, an evaluation of the extent of CD147 expression in cancer cell nests at the invasive tumor front may help in predicting cervical lymph node metastasis in patients with clinical N0 T1-T2 tongue SCC.
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spelling pubmed-56495302017-10-30 CD147 expression correlates with lymph node metastasis in T1-T2 squamous cell carcinoma of the tongue Suzuki, Shinsuke Honda, Kohei Nanjo, Hiroshi Iikawa, Nobuko Tsuji, Tadahiro Kawasaki, Yohei Yamazaki, Kazuharu Sato, Teruyuki Saito, Hidekazu Shiina, Kazuhiro Ishikawa, Kazuo Oncol Lett Articles Cervical lymph node metastasis causes a poor prognosis in cases of stage T1-T2 squamous cell carcinoma (SCC) of the tongue. Recent studies have reported that cluster of differentiation (CD)147, also known as extracellular matrix metalloproteinase inducer, contributes to tumor progression. The present study evaluated the role of CD147 in the tumorigenesis of SCC of the tongue in vitro, as well as the association between CD147 expression and cervical lymph node metastasis in clinical samples of SCC of the tongue. Tongue SCC cell lines were used to evaluate in vitro tumorigenesis. In addition, 41 patients with clinical stage T1-T2 tongue SCC were assessed with a histopathological analysis. Univariate and multivariate analysis were performed to investigate the risk of cervical lymph node metastasis associated with histopathological findings. In the in vitro study, cell invasiveness was upregulated by S100 calcium-binding protein A9 (S100A9) stimulation and downregulated following CD147-blocking antibody treatment. The univariate and multivariate analyses identified CD147 expression in the invasive tumor front as an independent risk factor for metastasis. It was concluded that CD147 induces tongue carcinoma cell invasion through its interaction with S100A9. Thus, an evaluation of the extent of CD147 expression in cancer cell nests at the invasive tumor front may help in predicting cervical lymph node metastasis in patients with clinical N0 T1-T2 tongue SCC. D.A. Spandidos 2017-10 2017-08-24 /pmc/articles/PMC5649530/ /pubmed/29085466 http://dx.doi.org/10.3892/ol.2017.6808 Text en Copyright: © Suzuki et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Suzuki, Shinsuke
Honda, Kohei
Nanjo, Hiroshi
Iikawa, Nobuko
Tsuji, Tadahiro
Kawasaki, Yohei
Yamazaki, Kazuharu
Sato, Teruyuki
Saito, Hidekazu
Shiina, Kazuhiro
Ishikawa, Kazuo
CD147 expression correlates with lymph node metastasis in T1-T2 squamous cell carcinoma of the tongue
title CD147 expression correlates with lymph node metastasis in T1-T2 squamous cell carcinoma of the tongue
title_full CD147 expression correlates with lymph node metastasis in T1-T2 squamous cell carcinoma of the tongue
title_fullStr CD147 expression correlates with lymph node metastasis in T1-T2 squamous cell carcinoma of the tongue
title_full_unstemmed CD147 expression correlates with lymph node metastasis in T1-T2 squamous cell carcinoma of the tongue
title_short CD147 expression correlates with lymph node metastasis in T1-T2 squamous cell carcinoma of the tongue
title_sort cd147 expression correlates with lymph node metastasis in t1-t2 squamous cell carcinoma of the tongue
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5649530/
https://www.ncbi.nlm.nih.gov/pubmed/29085466
http://dx.doi.org/10.3892/ol.2017.6808
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