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Expression of the extracellular sulfatase SULF2 is associated with squamous cell carcinoma of the head and neck

Sulfatase 2 (SULF2), an extracellular sulfatase that alters sulfation on heparan sulfate proteoglycans, is involved in the tumorigenesis and progression of several carcinomas. SULF2 expression has not been evaluated in squamous cell carcinoma of the head and neck (HNSCC). Here we report results of I...

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Autores principales: Flowers, Sarah A., Zhou, Xin, Wu, Jing, Wang, Yiwen, Makambi, Kepher, Kallakury, Bhaskar V., Singer, Mark S., Rosen, Steven D., Davidson, Bruce, Goldman, Radoslav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5190016/
https://www.ncbi.nlm.nih.gov/pubmed/27223083
http://dx.doi.org/10.18632/oncotarget.9506
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author Flowers, Sarah A.
Zhou, Xin
Wu, Jing
Wang, Yiwen
Makambi, Kepher
Kallakury, Bhaskar V.
Singer, Mark S.
Rosen, Steven D.
Davidson, Bruce
Goldman, Radoslav
author_facet Flowers, Sarah A.
Zhou, Xin
Wu, Jing
Wang, Yiwen
Makambi, Kepher
Kallakury, Bhaskar V.
Singer, Mark S.
Rosen, Steven D.
Davidson, Bruce
Goldman, Radoslav
author_sort Flowers, Sarah A.
collection PubMed
description Sulfatase 2 (SULF2), an extracellular sulfatase that alters sulfation on heparan sulfate proteoglycans, is involved in the tumorigenesis and progression of several carcinomas. SULF2 expression has not been evaluated in squamous cell carcinoma of the head and neck (HNSCC). Here we report results of IHC of SULF2 expression in HNSCC tissue. SULF2 was detected in 57% of tumors (n = 40) with a significant increase in intensity and number of stained cells compared to adjacent cancer-free tissue (p-value < 0.01), increasing with cancer stage when comparing stages 1 and 2 to stages 3 and 4 (p-value 0.01). SULF2 was not detected in epithelial cells of cancer-free controls, and expression was independent of patient demographics, tumor location and etiological factors, smoking and HPV infection by p16 IHC analysis. Sandwich ELISA was performed on serum of HNSCC patients (n = 28) and controls (n = 35), and although SULF2 was detectable, no change was observed in HNSCC. Saliva, collected by mouthwash, from HNSCC patients (n = 8) and controls (n = 8) was also tested by ELISA in a preliminary investigation and an increase in SULF2 was observed in HNSCC (p-value 0.041). Overall, this study shows that SULF2 is increased in HNSCC independent of tissue location (oral cavity, oropharynx, larynx and hypopharynx), patient demographics and etiology. Although no change in SULF2 was detected in HNSCC serum, its detection in saliva makes it worthy of further investigation as a potential HNSCC biomarker.
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spelling pubmed-51900162017-01-05 Expression of the extracellular sulfatase SULF2 is associated with squamous cell carcinoma of the head and neck Flowers, Sarah A. Zhou, Xin Wu, Jing Wang, Yiwen Makambi, Kepher Kallakury, Bhaskar V. Singer, Mark S. Rosen, Steven D. Davidson, Bruce Goldman, Radoslav Oncotarget Research Paper Sulfatase 2 (SULF2), an extracellular sulfatase that alters sulfation on heparan sulfate proteoglycans, is involved in the tumorigenesis and progression of several carcinomas. SULF2 expression has not been evaluated in squamous cell carcinoma of the head and neck (HNSCC). Here we report results of IHC of SULF2 expression in HNSCC tissue. SULF2 was detected in 57% of tumors (n = 40) with a significant increase in intensity and number of stained cells compared to adjacent cancer-free tissue (p-value < 0.01), increasing with cancer stage when comparing stages 1 and 2 to stages 3 and 4 (p-value 0.01). SULF2 was not detected in epithelial cells of cancer-free controls, and expression was independent of patient demographics, tumor location and etiological factors, smoking and HPV infection by p16 IHC analysis. Sandwich ELISA was performed on serum of HNSCC patients (n = 28) and controls (n = 35), and although SULF2 was detectable, no change was observed in HNSCC. Saliva, collected by mouthwash, from HNSCC patients (n = 8) and controls (n = 8) was also tested by ELISA in a preliminary investigation and an increase in SULF2 was observed in HNSCC (p-value 0.041). Overall, this study shows that SULF2 is increased in HNSCC independent of tissue location (oral cavity, oropharynx, larynx and hypopharynx), patient demographics and etiology. Although no change in SULF2 was detected in HNSCC serum, its detection in saliva makes it worthy of further investigation as a potential HNSCC biomarker. Impact Journals LLC 2016-05-20 /pmc/articles/PMC5190016/ /pubmed/27223083 http://dx.doi.org/10.18632/oncotarget.9506 Text en Copyright: © 2016 Flowers et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Flowers, Sarah A.
Zhou, Xin
Wu, Jing
Wang, Yiwen
Makambi, Kepher
Kallakury, Bhaskar V.
Singer, Mark S.
Rosen, Steven D.
Davidson, Bruce
Goldman, Radoslav
Expression of the extracellular sulfatase SULF2 is associated with squamous cell carcinoma of the head and neck
title Expression of the extracellular sulfatase SULF2 is associated with squamous cell carcinoma of the head and neck
title_full Expression of the extracellular sulfatase SULF2 is associated with squamous cell carcinoma of the head and neck
title_fullStr Expression of the extracellular sulfatase SULF2 is associated with squamous cell carcinoma of the head and neck
title_full_unstemmed Expression of the extracellular sulfatase SULF2 is associated with squamous cell carcinoma of the head and neck
title_short Expression of the extracellular sulfatase SULF2 is associated with squamous cell carcinoma of the head and neck
title_sort expression of the extracellular sulfatase sulf2 is associated with squamous cell carcinoma of the head and neck
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5190016/
https://www.ncbi.nlm.nih.gov/pubmed/27223083
http://dx.doi.org/10.18632/oncotarget.9506
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