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Amplification of Chromosome 8 Genes in Lung Cancer

Chromosomal alterations are frequent events in lung carcinogenesis and usually display regions of focal amplification containing several overexpressed oncogenes. Although gains and losses of chromosomal loci have been reported copy number changes of the individual genes have not been analyzed in lun...

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Autores principales: Baykara, Onur, Bakir, Burak, Buyru, Nur, Kaynak, Kamil, Dalay, Nejat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4317763/
https://www.ncbi.nlm.nih.gov/pubmed/25663945
http://dx.doi.org/10.7150/jca.10638
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author Baykara, Onur
Bakir, Burak
Buyru, Nur
Kaynak, Kamil
Dalay, Nejat
author_facet Baykara, Onur
Bakir, Burak
Buyru, Nur
Kaynak, Kamil
Dalay, Nejat
author_sort Baykara, Onur
collection PubMed
description Chromosomal alterations are frequent events in lung carcinogenesis and usually display regions of focal amplification containing several overexpressed oncogenes. Although gains and losses of chromosomal loci have been reported copy number changes of the individual genes have not been analyzed in lung cancer. In this study 22 genes were analyzed by MLPA in tumors and matched normal tissue samples from 82 patients with non-small cell lung cancer. Gene amplifications were observed in 84% of the samples. Chromosome 8 was found to harbor the most frequent copy number alterations. The most frequently amplified genes were ZNF703, PRDM14 and MYC on chromosome 8 and the BIRC5 gene on chromosome 17. The frequency of deletions were much lower and the most frequently deleted gene was ADAM9. Amplification of the ZNF703, PRDM14 and MYC genes were highly correlated suggesting that the genes displaying high copy number changes on chromosome 8 collaborate during lung carcinogenesis.
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spelling pubmed-43177632015-02-06 Amplification of Chromosome 8 Genes in Lung Cancer Baykara, Onur Bakir, Burak Buyru, Nur Kaynak, Kamil Dalay, Nejat J Cancer Research Paper Chromosomal alterations are frequent events in lung carcinogenesis and usually display regions of focal amplification containing several overexpressed oncogenes. Although gains and losses of chromosomal loci have been reported copy number changes of the individual genes have not been analyzed in lung cancer. In this study 22 genes were analyzed by MLPA in tumors and matched normal tissue samples from 82 patients with non-small cell lung cancer. Gene amplifications were observed in 84% of the samples. Chromosome 8 was found to harbor the most frequent copy number alterations. The most frequently amplified genes were ZNF703, PRDM14 and MYC on chromosome 8 and the BIRC5 gene on chromosome 17. The frequency of deletions were much lower and the most frequently deleted gene was ADAM9. Amplification of the ZNF703, PRDM14 and MYC genes were highly correlated suggesting that the genes displaying high copy number changes on chromosome 8 collaborate during lung carcinogenesis. Ivyspring International Publisher 2015-01-20 /pmc/articles/PMC4317763/ /pubmed/25663945 http://dx.doi.org/10.7150/jca.10638 Text en © 2015 Ivyspring International Publisher. Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited. See http://ivyspring.com/terms for terms and conditions.
spellingShingle Research Paper
Baykara, Onur
Bakir, Burak
Buyru, Nur
Kaynak, Kamil
Dalay, Nejat
Amplification of Chromosome 8 Genes in Lung Cancer
title Amplification of Chromosome 8 Genes in Lung Cancer
title_full Amplification of Chromosome 8 Genes in Lung Cancer
title_fullStr Amplification of Chromosome 8 Genes in Lung Cancer
title_full_unstemmed Amplification of Chromosome 8 Genes in Lung Cancer
title_short Amplification of Chromosome 8 Genes in Lung Cancer
title_sort amplification of chromosome 8 genes in lung cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4317763/
https://www.ncbi.nlm.nih.gov/pubmed/25663945
http://dx.doi.org/10.7150/jca.10638
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