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Methylation of 14-3-3σ gene and prognostic significance of 14-3-3σ expression in non-small cell lung cancer

Loss of 14-3-3σ expression through DNA methylation has been associated with carcinogenesis and the prognosis for various cancer types. Detection of methylation of the gene in serum may be useful for diagnostic utility. The present study aimed to investigate the correlation between 14-3-3σ methylatio...

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Autores principales: Raungrut, Pritsana, Petjaroen, Pingpond, Geater, Sarayut Lucien, Keeratichananont, Warangkana, Phukaoloun, Monlika, Suwiwat, Supaporn, Thongsuksai, Paramee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662907/
https://www.ncbi.nlm.nih.gov/pubmed/29113161
http://dx.doi.org/10.3892/ol.2017.6881
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author Raungrut, Pritsana
Petjaroen, Pingpond
Geater, Sarayut Lucien
Keeratichananont, Warangkana
Phukaoloun, Monlika
Suwiwat, Supaporn
Thongsuksai, Paramee
author_facet Raungrut, Pritsana
Petjaroen, Pingpond
Geater, Sarayut Lucien
Keeratichananont, Warangkana
Phukaoloun, Monlika
Suwiwat, Supaporn
Thongsuksai, Paramee
author_sort Raungrut, Pritsana
collection PubMed
description Loss of 14-3-3σ expression through DNA methylation has been associated with carcinogenesis and the prognosis for various cancer types. Detection of methylation of the gene in serum may be useful for diagnostic utility. The present study aimed to investigate the correlation between 14-3-3σ methylation level in 36 paired tumor tissues of non-small cell lung cancer (NSCLC) and matched serum using methylation-specific polymerase chain reaction. The prognostic significance of 14-3-3σ expression in 167 NSCLC was also evaluated using immunohistochemistry. Methylation of the 14-3-3σ gene was identified in all samples. The methylation level in the serum (mean 87.7%, range 64.6–100%) was higher compared with tumor (mean 46.7%, range 25.3–56.3%). However, no significant correlation between methylation levels in tissues and serums was observed (Spearman's correlation, −0.036; P=0.837). In the 167 tumor tissues, the majority of the cases (83.8%) exhibited negative expression. Adenocarcinoma is more likely to exhibit negative expression (91.4%) compared with squamous cell carcinoma (70.2%). No significant difference was identified in the overall survival according to 14-3-3σ expression status and 14-3-3σ expression did not demonstrated independent prognostic significance. In conclusion, NSCLC harbors certain levels of 14-3-3σ methylation in the tumor and the sera of patients. The clinical value of serum 14-3-3σ methylation should be further elucidated. Immunohistochemical expression 14-3-3σ protein has limited value on prognostic significance.
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spelling pubmed-56629072017-11-06 Methylation of 14-3-3σ gene and prognostic significance of 14-3-3σ expression in non-small cell lung cancer Raungrut, Pritsana Petjaroen, Pingpond Geater, Sarayut Lucien Keeratichananont, Warangkana Phukaoloun, Monlika Suwiwat, Supaporn Thongsuksai, Paramee Oncol Lett Articles Loss of 14-3-3σ expression through DNA methylation has been associated with carcinogenesis and the prognosis for various cancer types. Detection of methylation of the gene in serum may be useful for diagnostic utility. The present study aimed to investigate the correlation between 14-3-3σ methylation level in 36 paired tumor tissues of non-small cell lung cancer (NSCLC) and matched serum using methylation-specific polymerase chain reaction. The prognostic significance of 14-3-3σ expression in 167 NSCLC was also evaluated using immunohistochemistry. Methylation of the 14-3-3σ gene was identified in all samples. The methylation level in the serum (mean 87.7%, range 64.6–100%) was higher compared with tumor (mean 46.7%, range 25.3–56.3%). However, no significant correlation between methylation levels in tissues and serums was observed (Spearman's correlation, −0.036; P=0.837). In the 167 tumor tissues, the majority of the cases (83.8%) exhibited negative expression. Adenocarcinoma is more likely to exhibit negative expression (91.4%) compared with squamous cell carcinoma (70.2%). No significant difference was identified in the overall survival according to 14-3-3σ expression status and 14-3-3σ expression did not demonstrated independent prognostic significance. In conclusion, NSCLC harbors certain levels of 14-3-3σ methylation in the tumor and the sera of patients. The clinical value of serum 14-3-3σ methylation should be further elucidated. Immunohistochemical expression 14-3-3σ protein has limited value on prognostic significance. D.A. Spandidos 2017-11 2017-09-04 /pmc/articles/PMC5662907/ /pubmed/29113161 http://dx.doi.org/10.3892/ol.2017.6881 Text en Copyright: © Raungrut 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
Raungrut, Pritsana
Petjaroen, Pingpond
Geater, Sarayut Lucien
Keeratichananont, Warangkana
Phukaoloun, Monlika
Suwiwat, Supaporn
Thongsuksai, Paramee
Methylation of 14-3-3σ gene and prognostic significance of 14-3-3σ expression in non-small cell lung cancer
title Methylation of 14-3-3σ gene and prognostic significance of 14-3-3σ expression in non-small cell lung cancer
title_full Methylation of 14-3-3σ gene and prognostic significance of 14-3-3σ expression in non-small cell lung cancer
title_fullStr Methylation of 14-3-3σ gene and prognostic significance of 14-3-3σ expression in non-small cell lung cancer
title_full_unstemmed Methylation of 14-3-3σ gene and prognostic significance of 14-3-3σ expression in non-small cell lung cancer
title_short Methylation of 14-3-3σ gene and prognostic significance of 14-3-3σ expression in non-small cell lung cancer
title_sort methylation of 14-3-3σ gene and prognostic significance of 14-3-3σ expression in non-small cell lung cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662907/
https://www.ncbi.nlm.nih.gov/pubmed/29113161
http://dx.doi.org/10.3892/ol.2017.6881
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