Early onset lung cancer, cigarette smoking and the SNP309 of the murine double minute-2 (MDM2) gene
Creators
- Mittelstrass, Kirstin1
- Woelke, Gabi1
- Cebulla, Mathias2
- Degen, Maria3
- Morr, Harald4
- Drings, Peter5
- Groeschel, Andreas6
- Kreymborg, Karsten Grosse7
- Haeußinger, Karl8
- Hoeffken, Gerd9
- Schmidt, Christine9
- Sauter, Wiebke1
- Jilge, Bettina10
- Schmidt, Wilhelm10
- Ko, You-Dschun11
- Taeuscher, Dagmar12
- Chang-Claude, Jenny13
- Wichmann, Heinz-Erich14, 1
- Bickeboeller, Heike15
- Risch, Angela13
- Rosenberger, Albert15
- Illig, Thomas1
- Timofeeva, Maria13
- Klopp, Norman1
- Dienemann, Hendrik5
- Meese, Eckart16
- Sybrecht, Gerhard6
- 1. Helmholtz Center Munich, German Research Center for Environmental Health, Institute of Epidemiology, Munich/Neuherberg (Germany)
- 2. Municipal Hospital "Sankt Georg", Leipzig (Germany)
- 3. Clinic of Pneumology, Waldhof Elgershausen, Greifenstein (Germany)
- 4. Department Internal Medicine-Oncology, Thorax-Clinic Heidelberg GmbH, Heidelberg (Germany)
- 5. Thoraxklinik Heidelberg GmbH, Heidelberg (Germany)
- 6. Institute of Internal Medicine V, Medical School, University of the Saarland (Germany)
- 7. Centre for Internal Medicine, University Hospital Leipzig (Germany)
- 8. Clinic of Pneumology München-Gauting, Munich (Germany)
- 9. Clinic Coswig GmbH, Division Internal Medicine, Coswig (Germany)
- 10. Chemnitz Hospital, Clinic for Internal Medicine, Chemnitz (Germany)
- 11. Department of Oncology, University Hospital of Bonn (Germany)
- 12. Wald-Hospital Gera GmbH, II. Medical Clinic, Gera (Germany)
- 13. German Cancer Research Centre (DKFZ), Heidelberg (Germany)
- 14. Ludwig-Maximilians-University of Munich, Institute of Medical Data Management, Biometrics and Epidemiology (Germany)
- 15. Department of Genetic Epidemiology, Georg-August University of Göttingen, Medical School, Göttingen (Germany)
- 16. Institute of Human Genetics, University of the Saarland (Germany)
Description
The polymorphism SNP309 (rs2279744) in the promoter region of the MDM2 gene has been shown to alter protein expression and may play a role in the susceptibility to lung cancer. The MDM2 protein is a key inhibitor of p53 and several mechanisms of MDM2/p53 interactions are presently known: modulating DNA-repair, cell-cycle control, cell growth and apoptosis. We used 635 Caucasian patients diagnosed with lung cancer before 51 years of age and 1300 healthy gender and age frequency matched population Caucasian controls to investigate the association between the MDM2 SNP309 and the risk of developing early onset lung cancer. Conditional logistic models were applied to assess the genotype-phenotype association, adjusted for smoking. Compared to the GG genotype, the adjusted ORs for the TG and TT genotype were 0.9 (95% CI: 0.7–1.5) and 1.0 (95% CI: 0.7–1.5), respectively. Also no association was found for histological subtypes of lung cancer. The strength of this study is that within young cases the genetic component to develop lung cancer may be greater. Our results indicate that the MDM2 SNP309 is not significantly associated with lung carcinogenesis but point towards gender-specific differences
Availability note (English)
Available from http://dx.doi.org/10.1186/1471-2407-8-113; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2377274Additional details
Identifiers
Publishing Information
- Journal Title
- BMC cancer (Online)
- Journal Volume
- 8
- Journal Page Range
- p. 113
- ISSN
- 1471-2407
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 46091931
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- APOPTOSIS; CARCINOGENESIS; CELL CYCLE; DNA REPAIR; GENES; GENOTYPE; GROWTH; HAZARDS; LUNGS; NEOPLASMS; PATIENTS; PHENOTYPE; PROTEINS
- Descriptors DEC
- BIOLOGICAL RECOVERY; BIOLOGICAL REPAIR; BODY; DISEASES; ORGANIC COMPOUNDS; ORGANS; PATHOGENESIS; REPAIR; RESPIRATORY SYSTEM
Optional Information
- Copyright
- Copyright (c) 2008 Mittelstrass et al
- Notes
- PMCID: PMC2377274; PUBLISHER-ID: 1471-2407-8-113; PMID: 18433484; OAI: oai:pubmedcentral.nih.gov:2377274; licensee BioMed Central Ltd.