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The overexpression of salivary cytokeratins as potential diagnostic biomarkers in head and neck squamous cell carcinomas

BACKGROUND: Cytokeratin (CK) intermediate filaments are demonstrated to have enormous potential in regulating cellular motility and cancer progression. There are more than 20 divergent CKs that have been identified, of which CK 8, 17, 18 and 19 are reported to be elevated in the tumour biopsies of h...

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Autores principales: Tang, Kai Dun, Kenny, Liz, Perry, Chris, Frazer, Ian, Punyadeera, Chamindie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5641129/
https://www.ncbi.nlm.nih.gov/pubmed/29069786
http://dx.doi.org/10.18632/oncotarget.19731
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author Tang, Kai Dun
Kenny, Liz
Perry, Chris
Frazer, Ian
Punyadeera, Chamindie
author_facet Tang, Kai Dun
Kenny, Liz
Perry, Chris
Frazer, Ian
Punyadeera, Chamindie
author_sort Tang, Kai Dun
collection PubMed
description BACKGROUND: Cytokeratin (CK) intermediate filaments are demonstrated to have enormous potential in regulating cellular motility and cancer progression. There are more than 20 divergent CKs that have been identified, of which CK 8, 17, 18 and 19 are reported to be elevated in the tumour biopsies of head and neck cancer squamous cell carcinoma (HNSCC) patients. However, CK expression profiles in the saliva of HNSCC patients have not been investigated. We aim to investigate the mRNA expression profiles of CKs in saliva collected from healthy controls, HPV-negative and -positive HNSCC patients. METHODS: Oral rinse samples were collected from 42 cancer-free healthy controls (age-matched) and patients who have been diagnosed with HPV-negative (n = 20) and -positive (n = 48) HNSCC. RESULTS: Here, we report that the mRNA expression profiles of CKs differed in saliva collected from healthy controls and HNSCC patients. The mRNA expression levels of CK 8 and 18 were significantly elevated in saliva collected from HPV-negative HNSCC patients; whilst, CK 17 and 19 were expressed at a higher mRNA level in saliva collected from HPV-positive HNSCC patients compared to healthy controls. Importantly, receiver operating characteristic (ROC) analysis showed salivary CK 8 and 18 to have superior sensitivity and specificity in discriminating the HPV-negative HNSCC patients from healthy controls (80% and 86%) as well as between HPV-negative and -positive HNSCC patients (75% and 81%). CONCLUSION: In summary, we have demonstrated that an aberrant expression of salivary CKs may serve as a potential non-invasive diagnostic biomarker in HNSCC.
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spelling pubmed-56411292017-10-24 The overexpression of salivary cytokeratins as potential diagnostic biomarkers in head and neck squamous cell carcinomas Tang, Kai Dun Kenny, Liz Perry, Chris Frazer, Ian Punyadeera, Chamindie Oncotarget Research Paper BACKGROUND: Cytokeratin (CK) intermediate filaments are demonstrated to have enormous potential in regulating cellular motility and cancer progression. There are more than 20 divergent CKs that have been identified, of which CK 8, 17, 18 and 19 are reported to be elevated in the tumour biopsies of head and neck cancer squamous cell carcinoma (HNSCC) patients. However, CK expression profiles in the saliva of HNSCC patients have not been investigated. We aim to investigate the mRNA expression profiles of CKs in saliva collected from healthy controls, HPV-negative and -positive HNSCC patients. METHODS: Oral rinse samples were collected from 42 cancer-free healthy controls (age-matched) and patients who have been diagnosed with HPV-negative (n = 20) and -positive (n = 48) HNSCC. RESULTS: Here, we report that the mRNA expression profiles of CKs differed in saliva collected from healthy controls and HNSCC patients. The mRNA expression levels of CK 8 and 18 were significantly elevated in saliva collected from HPV-negative HNSCC patients; whilst, CK 17 and 19 were expressed at a higher mRNA level in saliva collected from HPV-positive HNSCC patients compared to healthy controls. Importantly, receiver operating characteristic (ROC) analysis showed salivary CK 8 and 18 to have superior sensitivity and specificity in discriminating the HPV-negative HNSCC patients from healthy controls (80% and 86%) as well as between HPV-negative and -positive HNSCC patients (75% and 81%). CONCLUSION: In summary, we have demonstrated that an aberrant expression of salivary CKs may serve as a potential non-invasive diagnostic biomarker in HNSCC. Impact Journals LLC 2017-07-31 /pmc/articles/PMC5641129/ /pubmed/29069786 http://dx.doi.org/10.18632/oncotarget.19731 Text en Copyright: © 2017 Tang et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Tang, Kai Dun
Kenny, Liz
Perry, Chris
Frazer, Ian
Punyadeera, Chamindie
The overexpression of salivary cytokeratins as potential diagnostic biomarkers in head and neck squamous cell carcinomas
title The overexpression of salivary cytokeratins as potential diagnostic biomarkers in head and neck squamous cell carcinomas
title_full The overexpression of salivary cytokeratins as potential diagnostic biomarkers in head and neck squamous cell carcinomas
title_fullStr The overexpression of salivary cytokeratins as potential diagnostic biomarkers in head and neck squamous cell carcinomas
title_full_unstemmed The overexpression of salivary cytokeratins as potential diagnostic biomarkers in head and neck squamous cell carcinomas
title_short The overexpression of salivary cytokeratins as potential diagnostic biomarkers in head and neck squamous cell carcinomas
title_sort overexpression of salivary cytokeratins as potential diagnostic biomarkers in head and neck squamous cell carcinomas
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5641129/
https://www.ncbi.nlm.nih.gov/pubmed/29069786
http://dx.doi.org/10.18632/oncotarget.19731
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