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Effect of trail C1595T variant and gene expression on the pathogenesis of non-small cell lung cancer

It is known that disorders in apoptosis function play an important role in the pathogenesis of many types of cancer, including lung cancer. Tumor necrosis factor related apoptosis inducing ligand (TRAIL), a type II transmembrane protein, is a death ligand capable of inducing apoptosis by activating...

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Autores principales: Koç Erbaşoğlu, Öncü, Horozoğlu, Cem, Ercan, Şeyda, Kara, Hasan Volkan, Turna, Akif, Farooqi, Ammad Ahmad, Yaylım, İlhan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263097/
https://www.ncbi.nlm.nih.gov/pubmed/30481147
http://dx.doi.org/10.1080/19932820.2018.1535746
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author Koç Erbaşoğlu, Öncü
Horozoğlu, Cem
Ercan, Şeyda
Kara, Hasan Volkan
Turna, Akif
Farooqi, Ammad Ahmad
Yaylım, İlhan
author_facet Koç Erbaşoğlu, Öncü
Horozoğlu, Cem
Ercan, Şeyda
Kara, Hasan Volkan
Turna, Akif
Farooqi, Ammad Ahmad
Yaylım, İlhan
author_sort Koç Erbaşoğlu, Öncü
collection PubMed
description It is known that disorders in apoptosis function play an important role in the pathogenesis of many types of cancer, including lung cancer. Tumor necrosis factor related apoptosis inducing ligand (TRAIL), a type II transmembrane protein, is a death ligand capable of inducing apoptosis by activating distinctive death receptor. Our purpose in this study is to investigate the gene polymorphisms in TRAIL molecular pathway and TRAIL gene expression levels in non-small cell lung cancer (NSCLC) patients in terms of pathogenesis and prognosis of the disease. In this study, TRAIL C1595T polymorphism was genotyped using polymerase chain reaction-restriction fragment length polymorphism analysis in 158 patients with NSCLC and 98 healthy individuals. Surgically resected tissues were examined and classified histopathologically. In addition, TRAIL gene expression levels in tumor tissue and tumor surrounding tissue samples of 48 patients with NSCLC were determined using real-time polymerase chain reaction. TRAIL gene expression levels of NSCLC patients were detected significantly 28.8 fold decrease in the tumor tissue group compared to the control group (p=0.026). When patients were compared to tumor stage, expression of TRAIL gene in advanced tumor stage was found to be significantly 7.86 fold higher than early tumor stage [p=0.028]. No significant relationship was found between NSCLC predisposition and prognostic parameters of NSCLC with TRAIL genotypes, but the frequency of TRAIL gene 1595 CT genotype was observed to be lower in the patients compared to the other genotypes, and the difference was found to be very close to statistical significance (p=0.07). It can be suggested that TRAIL may play an important role in the development of NSCLC and may be an effective prognostic factor in tumor progression.: It is known that disorders in apoptosis function play an important role in the pathogenesis of many types of cancer, including lung cancer. Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL), a type II transmembrane protein, is a death ligand capable of inducing apoptosis by activating distinctive death receptor. Our purpose in this study is to investigate the gene polymorphisms in TRAIL molecular pathway and TRAIL gene expression levels in non-small cell lung cancer (NSCLC) patients in terms of pathogenesis and prognosis of the disease.
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spelling pubmed-62630972018-12-03 Effect of trail C1595T variant and gene expression on the pathogenesis of non-small cell lung cancer Koç Erbaşoğlu, Öncü Horozoğlu, Cem Ercan, Şeyda Kara, Hasan Volkan Turna, Akif Farooqi, Ammad Ahmad Yaylım, İlhan Libyan J Med Original Article It is known that disorders in apoptosis function play an important role in the pathogenesis of many types of cancer, including lung cancer. Tumor necrosis factor related apoptosis inducing ligand (TRAIL), a type II transmembrane protein, is a death ligand capable of inducing apoptosis by activating distinctive death receptor. Our purpose in this study is to investigate the gene polymorphisms in TRAIL molecular pathway and TRAIL gene expression levels in non-small cell lung cancer (NSCLC) patients in terms of pathogenesis and prognosis of the disease. In this study, TRAIL C1595T polymorphism was genotyped using polymerase chain reaction-restriction fragment length polymorphism analysis in 158 patients with NSCLC and 98 healthy individuals. Surgically resected tissues were examined and classified histopathologically. In addition, TRAIL gene expression levels in tumor tissue and tumor surrounding tissue samples of 48 patients with NSCLC were determined using real-time polymerase chain reaction. TRAIL gene expression levels of NSCLC patients were detected significantly 28.8 fold decrease in the tumor tissue group compared to the control group (p=0.026). When patients were compared to tumor stage, expression of TRAIL gene in advanced tumor stage was found to be significantly 7.86 fold higher than early tumor stage [p=0.028]. No significant relationship was found between NSCLC predisposition and prognostic parameters of NSCLC with TRAIL genotypes, but the frequency of TRAIL gene 1595 CT genotype was observed to be lower in the patients compared to the other genotypes, and the difference was found to be very close to statistical significance (p=0.07). It can be suggested that TRAIL may play an important role in the development of NSCLC and may be an effective prognostic factor in tumor progression.: It is known that disorders in apoptosis function play an important role in the pathogenesis of many types of cancer, including lung cancer. Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL), a type II transmembrane protein, is a death ligand capable of inducing apoptosis by activating distinctive death receptor. Our purpose in this study is to investigate the gene polymorphisms in TRAIL molecular pathway and TRAIL gene expression levels in non-small cell lung cancer (NSCLC) patients in terms of pathogenesis and prognosis of the disease. Taylor & Francis 2018-11-27 /pmc/articles/PMC6263097/ /pubmed/30481147 http://dx.doi.org/10.1080/19932820.2018.1535746 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Koç Erbaşoğlu, Öncü
Horozoğlu, Cem
Ercan, Şeyda
Kara, Hasan Volkan
Turna, Akif
Farooqi, Ammad Ahmad
Yaylım, İlhan
Effect of trail C1595T variant and gene expression on the pathogenesis of non-small cell lung cancer
title Effect of trail C1595T variant and gene expression on the pathogenesis of non-small cell lung cancer
title_full Effect of trail C1595T variant and gene expression on the pathogenesis of non-small cell lung cancer
title_fullStr Effect of trail C1595T variant and gene expression on the pathogenesis of non-small cell lung cancer
title_full_unstemmed Effect of trail C1595T variant and gene expression on the pathogenesis of non-small cell lung cancer
title_short Effect of trail C1595T variant and gene expression on the pathogenesis of non-small cell lung cancer
title_sort effect of trail c1595t variant and gene expression on the pathogenesis of non-small cell lung cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263097/
https://www.ncbi.nlm.nih.gov/pubmed/30481147
http://dx.doi.org/10.1080/19932820.2018.1535746
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