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Prognostic Impact of MiR-155 in Non-Small Cell Lung Cancer Evaluated by in Situ Hybridization

BACKGROUND: In recent years, microRNAs (miRNAs) have been found to play an essential role in tumor development. In lung tumorigenesis, targets and pathways of miRNAs are being revealed, and further translational research in this field is warranted. MiR-155 is one of the miRNAs most consistently invo...

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Autores principales: Donnem, Tom, Eklo, Katrine, Berg, Thomas, Sorbye, Sveinung W, Lonvik, Kenneth, Al-Saad, Samer, Al-Shibli, Khalid, Andersen, Sigve, Stenvold, Helge, Bremnes, Roy M, Busund, Lill-Tove
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3023703/
https://www.ncbi.nlm.nih.gov/pubmed/21219656
http://dx.doi.org/10.1186/1479-5876-9-6
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author Donnem, Tom
Eklo, Katrine
Berg, Thomas
Sorbye, Sveinung W
Lonvik, Kenneth
Al-Saad, Samer
Al-Shibli, Khalid
Andersen, Sigve
Stenvold, Helge
Bremnes, Roy M
Busund, Lill-Tove
author_facet Donnem, Tom
Eklo, Katrine
Berg, Thomas
Sorbye, Sveinung W
Lonvik, Kenneth
Al-Saad, Samer
Al-Shibli, Khalid
Andersen, Sigve
Stenvold, Helge
Bremnes, Roy M
Busund, Lill-Tove
author_sort Donnem, Tom
collection PubMed
description BACKGROUND: In recent years, microRNAs (miRNAs) have been found to play an essential role in tumor development. In lung tumorigenesis, targets and pathways of miRNAs are being revealed, and further translational research in this field is warranted. MiR-155 is one of the miRNAs most consistently involved in various neoplastic diseases. We aimed to investigate the prognostic impact of the multifunctional miR-155 in non-small cell lung cancer (NSCLC) patients. METHODS: Tumor tissue samples from 335 resected stage I to IIIA NSCLC patients were obtained and tissue microarrays (TMAs) were constructed with four cores from each tumor specimen. In situ hybridization (ISH) was used to evaluate the expression of miR-155. RESULTS: There were 191 squamous cell carcinomas (SCCs), 95 adenocarcinomas (ACs), 31 large cell carcinomas and 18 bronchioalveolar carcinomas. MiR-155 expression did not have a significant prognostic impact in the total cohort (P = 0.43). In ACs, high miR-155 expression tended to a significant negative prognostic effect on survival in univariate analysis (P = 0.086) and was an independent prognostic factor in multivariate analysis (HR 1.87, CI 95% 1.01 - 3.48, P = 0.047). In SCC patients with lymph node metastasis, however, miR-155 had a positive prognostic impact on survival in univariate (P = 0.034) as well as in multivariate (HR 0.45, CI 95% 0.21-0.96, P = 0.039) analysis. CONCLUSIONS: The prognostic impact of miR-155 depends on histological subtype and nodal status in NSCLC.
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spelling pubmed-30237032011-01-20 Prognostic Impact of MiR-155 in Non-Small Cell Lung Cancer Evaluated by in Situ Hybridization Donnem, Tom Eklo, Katrine Berg, Thomas Sorbye, Sveinung W Lonvik, Kenneth Al-Saad, Samer Al-Shibli, Khalid Andersen, Sigve Stenvold, Helge Bremnes, Roy M Busund, Lill-Tove J Transl Med Research BACKGROUND: In recent years, microRNAs (miRNAs) have been found to play an essential role in tumor development. In lung tumorigenesis, targets and pathways of miRNAs are being revealed, and further translational research in this field is warranted. MiR-155 is one of the miRNAs most consistently involved in various neoplastic diseases. We aimed to investigate the prognostic impact of the multifunctional miR-155 in non-small cell lung cancer (NSCLC) patients. METHODS: Tumor tissue samples from 335 resected stage I to IIIA NSCLC patients were obtained and tissue microarrays (TMAs) were constructed with four cores from each tumor specimen. In situ hybridization (ISH) was used to evaluate the expression of miR-155. RESULTS: There were 191 squamous cell carcinomas (SCCs), 95 adenocarcinomas (ACs), 31 large cell carcinomas and 18 bronchioalveolar carcinomas. MiR-155 expression did not have a significant prognostic impact in the total cohort (P = 0.43). In ACs, high miR-155 expression tended to a significant negative prognostic effect on survival in univariate analysis (P = 0.086) and was an independent prognostic factor in multivariate analysis (HR 1.87, CI 95% 1.01 - 3.48, P = 0.047). In SCC patients with lymph node metastasis, however, miR-155 had a positive prognostic impact on survival in univariate (P = 0.034) as well as in multivariate (HR 0.45, CI 95% 0.21-0.96, P = 0.039) analysis. CONCLUSIONS: The prognostic impact of miR-155 depends on histological subtype and nodal status in NSCLC. BioMed Central 2011-01-10 /pmc/articles/PMC3023703/ /pubmed/21219656 http://dx.doi.org/10.1186/1479-5876-9-6 Text en Copyright ©2011 Donnem 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 Research
Donnem, Tom
Eklo, Katrine
Berg, Thomas
Sorbye, Sveinung W
Lonvik, Kenneth
Al-Saad, Samer
Al-Shibli, Khalid
Andersen, Sigve
Stenvold, Helge
Bremnes, Roy M
Busund, Lill-Tove
Prognostic Impact of MiR-155 in Non-Small Cell Lung Cancer Evaluated by in Situ Hybridization
title Prognostic Impact of MiR-155 in Non-Small Cell Lung Cancer Evaluated by in Situ Hybridization
title_full Prognostic Impact of MiR-155 in Non-Small Cell Lung Cancer Evaluated by in Situ Hybridization
title_fullStr Prognostic Impact of MiR-155 in Non-Small Cell Lung Cancer Evaluated by in Situ Hybridization
title_full_unstemmed Prognostic Impact of MiR-155 in Non-Small Cell Lung Cancer Evaluated by in Situ Hybridization
title_short Prognostic Impact of MiR-155 in Non-Small Cell Lung Cancer Evaluated by in Situ Hybridization
title_sort prognostic impact of mir-155 in non-small cell lung cancer evaluated by in situ hybridization
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3023703/
https://www.ncbi.nlm.nih.gov/pubmed/21219656
http://dx.doi.org/10.1186/1479-5876-9-6
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