Document Detail


Increased risk of non-small cell lung cancer and frequency of somatic TP53 gene mutations in Pro72 carriers of TP53 Arg72Pro polymorphism.
MedLine Citation:
PMID:  16499995     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The aim of this study was to assess whether the TP53 Arg72Pro polymorphism is associated with an increased risk of non-small cell lung cancer (NSCLC). Additionally, in NSCLC patients, we investigated a potential association between this polymorphism and somatic TP53 gene mutations in tumour cells. The study group included 240 NSCLC patients who underwent curative pulmonary resection. The control group (576 healthy subjects) was matched for sex and cigarette smoking. TP53 Arg72Pro polymorphism was determined by denaturing high-performance liquid chromatography. Tumours from 157 NSCLC patients were analysed for mutation in TP53 exons 5-8 by single strand conformation polymorphism, followed by sequencing of samples with different band pattern. Tumours from the remaining 83 patients were subjected to a direct sequencing of TP53 exons 5-8. The proportion of Pro homo/heterozygotes versus Arg homozygotes was significantly higher in NSCLC patients (54%) than in controls (46%, p = 0.034). The crude odds ratio for NSCLC development in Pro72 allele carriers was 1.39 (95% CI: 1.03-1.88). When adjusted for sex, age and smoking status in the multivariate logistic regression model, odds ratio for NSCLC development was 1.28 (95% CI: 0.91-1.80). Somatic TP53 mutations were found in 62 out of 240 NSCLC patients (26%), more frequently in Pro carriers (31%) than in Arg homozygotes (20%, p = 0.06). These results indicate that the TP53 codon 72 Pro allele may increase the risk of NSCLC. Additionally, the correlation between Pro72 and somatic TP53 mutations suggests that Pro72 allele carriers may be predisposed to tumour development along a p53 associated form of NSCLC, a finding that warrants further investigations.
Authors:
Amelia Szymanowska; Ewa Jassem; Rafał Dziadziuszko; Ake Borg; Janusz Limon; Grazyna Kobierska-Gulida; Witold Rzyman; Jacek Jassem
Related Documents :
14989405 - Early and late neurodevelopmental influences in the prodrome to schizophrenia: contribu...
25282705 - A novel mutation of the nicotinic acetylcholine receptor gene chrna4 in a chinese patie...
Publication Detail:
Type:  Comparative Study; Journal Article; Research Support, Non-U.S. Gov't     Date:  2006-02-24
Journal Detail:
Title:  Lung cancer (Amsterdam, Netherlands)     Volume:  52     ISSN:  0169-5002     ISO Abbreviation:  Lung Cancer     Publication Date:  2006 Apr 
Date Detail:
Created Date:  2006-03-08     Completed Date:  2006-09-21     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  8800805     Medline TA:  Lung Cancer     Country:  Ireland    
Other Details:
Languages:  eng     Pagination:  9-14     Citation Subset:  IM    
Affiliation:
Department of Allergology, Medical University of Gdansk, Gdansk, Poland.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Adenocarcinoma / genetics
Arginine / genetics
Carcinoma, Large Cell / genetics
Carcinoma, Non-Small-Cell Lung / genetics*
Carcinoma, Squamous Cell / genetics
Female
Genetic Predisposition to Disease
Genotype
Heterozygote
Humans
Lung Neoplasms / genetics*
Male
Middle Aged
Mutation / genetics*
Polymorphism, Genetic*
Proline / genetics
Risk Factors
Tumor Suppressor Protein p53 / genetics*
Chemical
Reg. No./Substance:
0/Tumor Suppressor Protein p53; 147-85-3/Proline; 74-79-3/Arginine

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Polymorphisms in TGF-beta1 gene and the risk of lung cancer.
Next Document:  Post-chemotherapy gross tumor volume is predictive of survival in patients with stage III non-small ...