Evidence map›Paper›PMID 30481147›Full record

ArticleThe Libyan journal of medicine2019

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

Öncü Koç Erbaşoğlu, Cem Horozoğlu, Şeyda Ercan, Hasan Volkan Kara, Akif Turna, Ammad Ahmad Farooqi, İlhan Yaylım

Abstract read
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Article in The Libyan journal of medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

7 authors.

Öncü Koç Erbaşoğlua Department of Molecular Medicine , Institute for Aziz Sancar Experimental Medicine Research, İstanbul University , İstanbul , Turkey.
Cem Horozoğlub Department of Medical Services and Techniques , Vocational School of Health Services, İstanbul Gelişim University , İstanbul , Turkey.
Şeyda Ercana Department of Molecular Medicine , Institute for Aziz Sancar Experimental Medicine Research, İstanbul University , İstanbul , Turkey.
Hasan Volkan Karac Department of Thoracic Surgery , Cerrahpasa Medical School, İstanbul University , İstanbul , Turkey.ORCID http://orcid.org/0000-0001-7702-9731
Akif Turnac Department of Thoracic Surgery , Cerrahpasa Medical School, İstanbul University , İstanbul , Turkey.
Ammad Ahmad Farooqid Department of Molecular Oncology , Institute of Biomedical and Genetic Engineering (IBGE), KRL Hospital , Islamabad , Pakistan.
İlhan Yaylıma Department of Molecular Medicine , Institute for Aziz Sancar Experimental Medicine Research, İstanbul University , İstanbul , Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Gene Expression Regulation, NeoplasticAdultApoptosisCarcinoma, Non-Small-Cell LungFemaleGenotyping TechniquesHumansLung NeoplasmsMaleMiddle AgedPrognosisTNF-Related Apoptosis-Inducing LigandTNF-Related Apoptosis-Inducing LigandApoptosisgene expressionlung cancerpolymorphismReal-Time Polymerase Chain Reaction; TRAIL

Identifiers

PMID30481147
PMCPMC6263097

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.