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microRNA evaluation of unknown primary lesions in the head and neck

Unknown primary malignancy in the head and neck is not an infrequent diagnosis for patients with metastatic cervical lymph nodes. Although linked with a relatively good prognosis following radiation treatment, widespread radiation is coupled with significant morbidity. Altered microRNA (miRNA) expre...

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Autores principales: Barker, Emma V, Cervigne, Nilva K, Reis, Patricia P, Goswami, Rashmi S, Xu, Wei, Weinreb, Ilan, Irish, Jonathan C, Kamel-Reid, Suzanne
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2806863/
https://www.ncbi.nlm.nih.gov/pubmed/20028561
http://dx.doi.org/10.1186/1476-4598-8-127
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author Barker, Emma V
Cervigne, Nilva K
Reis, Patricia P
Goswami, Rashmi S
Xu, Wei
Weinreb, Ilan
Irish, Jonathan C
Kamel-Reid, Suzanne
author_facet Barker, Emma V
Cervigne, Nilva K
Reis, Patricia P
Goswami, Rashmi S
Xu, Wei
Weinreb, Ilan
Irish, Jonathan C
Kamel-Reid, Suzanne
author_sort Barker, Emma V
collection PubMed
description Unknown primary malignancy in the head and neck is not an infrequent diagnosis for patients with metastatic cervical lymph nodes. Although linked with a relatively good prognosis following radiation treatment, widespread radiation is coupled with significant morbidity. Altered microRNA (miRNA) expression has been associated with both cancer progression and metastasis. We sought to determine whether miRNA expression analysis could be used as a diagnostic tool to discover the primary site of malignancy, within the head and neck. We used quantitative real-time PCR to identify miRNA expression profiles of squamous cell carcinoma of the tonsil, base of tongue and post-nasal space, as well as their corresponding metastatic lymph nodes, from 6 patients. Our results revealed that each cancer maintained its expression profile between the primary site and the nodal metastasis (r = 0.82, p < 0.0001). In addition, each anatomical sub-site maintained a distinct miRNA profile between individual patients (r = 0.79, p < 0.0001). Finally, between sub-sites, the miRNA profiles were distinct (p < 0.0001). As proof of principle, our study provides an indication that miRNA expression analysis may be useful to compare the primary lesion and local metastatic disease. This may be clinically relevant to predict the primary site of origin of metastatic disease, when the primary site remains obscure.
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spelling pubmed-28068632010-01-15 microRNA evaluation of unknown primary lesions in the head and neck Barker, Emma V Cervigne, Nilva K Reis, Patricia P Goswami, Rashmi S Xu, Wei Weinreb, Ilan Irish, Jonathan C Kamel-Reid, Suzanne Mol Cancer Short communication Unknown primary malignancy in the head and neck is not an infrequent diagnosis for patients with metastatic cervical lymph nodes. Although linked with a relatively good prognosis following radiation treatment, widespread radiation is coupled with significant morbidity. Altered microRNA (miRNA) expression has been associated with both cancer progression and metastasis. We sought to determine whether miRNA expression analysis could be used as a diagnostic tool to discover the primary site of malignancy, within the head and neck. We used quantitative real-time PCR to identify miRNA expression profiles of squamous cell carcinoma of the tonsil, base of tongue and post-nasal space, as well as their corresponding metastatic lymph nodes, from 6 patients. Our results revealed that each cancer maintained its expression profile between the primary site and the nodal metastasis (r = 0.82, p < 0.0001). In addition, each anatomical sub-site maintained a distinct miRNA profile between individual patients (r = 0.79, p < 0.0001). Finally, between sub-sites, the miRNA profiles were distinct (p < 0.0001). As proof of principle, our study provides an indication that miRNA expression analysis may be useful to compare the primary lesion and local metastatic disease. This may be clinically relevant to predict the primary site of origin of metastatic disease, when the primary site remains obscure. BioMed Central 2009-12-23 /pmc/articles/PMC2806863/ /pubmed/20028561 http://dx.doi.org/10.1186/1476-4598-8-127 Text en Copyright ©2009 Barker et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short communication
Barker, Emma V
Cervigne, Nilva K
Reis, Patricia P
Goswami, Rashmi S
Xu, Wei
Weinreb, Ilan
Irish, Jonathan C
Kamel-Reid, Suzanne
microRNA evaluation of unknown primary lesions in the head and neck
title microRNA evaluation of unknown primary lesions in the head and neck
title_full microRNA evaluation of unknown primary lesions in the head and neck
title_fullStr microRNA evaluation of unknown primary lesions in the head and neck
title_full_unstemmed microRNA evaluation of unknown primary lesions in the head and neck
title_short microRNA evaluation of unknown primary lesions in the head and neck
title_sort microrna evaluation of unknown primary lesions in the head and neck
topic Short communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2806863/
https://www.ncbi.nlm.nih.gov/pubmed/20028561
http://dx.doi.org/10.1186/1476-4598-8-127
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