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Mutagenesis Advance Access originally published online on July 30, 2009
Mutagenesis 2009 24(6):475-480; doi:10.1093/mutage/gep031
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© The Author 2009. Published by Oxford University Press on behalf of the UK Environmental Mutagen Society. All rights reserved. For permissions, please e-mail: journals.permissions@oxfordjournals.org.

Relationship between TP53 tumour suppressor gene mutations and smoking-related bulky DNA adducts in a lung cancer study population from Hungary

Lívia Anna{dagger}, Reetta Holmila1,{dagger}, Katalin Kovács, Erika Gyorffy, Zoltán Gyori2, Judit Segesdi2, János Minárovits2, Ibolya Soltész3, Szilárd Kostic4,5, Attila Csekeo4, Kirsti Husgafvel-Pursiainen1 and Bernadette Schoket*

Department of Molecular Environmental Epidemiology, National Institute of Environmental Health, Budapest, Hungary 1Department of Biological Mechanisms and Prevention of Work-Related Diseases, Finnish Institute of Occupational Health, Helsinki, Finland 2Microbiological Research Group, National Center of Epidemiology, Budapest, Hungary 3Department of Pathology, Korányi National Institute of Pulmonology, Budapest, Hungary 4Department of Thoracic Surgery, Korányi National Institute of Pulmonology, Budapest, Hungary

Lung cancer rate in Hungary is one of the highest in the world among men and also very high among women, for reasons not clearly understood yet. The aim of the study was to explore characteristics of DNA damage and TP53 gene mutations in lung cancer from Hungary. Tissue samples from 104 lung resections for lung cancer patients, both men and women, operated on for non-small cell lung cancer, specifically, primary squamous cell carcinoma or adenocarcinoma were studied. Of the cases, 37% smoked up to the surgery, 24% stopped smoking within 1 year before the surgery, 26% stopped smoking more than a year before the surgery and 13% never smoked. TP53 mutations were detected by denaturant gradient gel electrophoresis, automated capillary electrophoresis single-strand conformation polymorphism and sequencing. Bulky DNA adduct levels were determined by 32P-post-labelling in non-tumorous lung tissue. In total, 45% (47/104) of the cases carried TP53 mutation. The prevalence of TP53 mutations was statistically significantly associated with duration of smoking, tumour histology and gender. Smokers had approximately twice as high bulky adduct level as the combined group of former- and never-smokers (10.9 ± 6.5 versus 5.5 ± 3.4 adducts/108 nucleotides). The common base change G -> T transversion (8/43; 19%) was detected exclusively in smokers. For the first time, we demonstrate that most carriers of G -> T transversions had also a high level of bulky DNA adducts in their non-tumourous lung tissue. Our study provides evidence for a high burden of molecular alterations occurring concurrently in the lung of lung cancer patients.

* To whom correspondence should be addressed. Department of Molecular Environmental Epidemiology, National Institute of Environmental Health, Gyáli út 2-6, H-1097 Budapest, Hungary. Tel: +36-1-476 1293; Fax: +36-1-215 0148; Email: schoket.bernadette{at}oki.antsz.hu


{dagger} The authors contributed equally to this work.

5 Present address: National Institute of Oncology, Budapest, Hungary

Received on July 7, 2009; accepted on July 9, 2009.


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