O6-alkylguanine-DNA alkyltransferase (MGMT) is a universal DNA repair protein involved in the DNA direct reversal repair pathway that copes with alkylating carcinogens. Reduced MGMT expression as well as enzyme activity may result in an increased susceptibility to cancers. To elucidate the role of s
Genetic variants in the MDM2 promoter and lung cancer risk in a Chinese population
β Scribed by Zhibin Hu; Hongxia Ma; Daru Lu; Ji Qian; Jiannong Zhou; Yijiang Chen; Lin Xu; Xinru Wang; Qingyi Wei; Hongbing Shen
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- French
- Weight
- 72 KB
- Volume
- 118
- Category
- Article
- ISSN
- 0020-7136
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β¦ Synopsis
Abstract
Overexpression of MDM2 may attenuate the P53 stress response pathway through direct blocking of P53 transcriptional activity and mediating P53 degradation. Two promoter polymorphisms (one is a T to G substitution at the intronic P53βresponse promoter, and the other is a 40βbp insertion/deletion polymorphism in the constitutive promoter) were identified, and recently the T/G substitution (SNP309) has been demonstrated to alter the levels of MDM2 gene products. In this molecular epidemiological study with 717 incident lung cancer cases and 1,083 cancerβfree controls, we genotyped these 2 promoter polymorphisms of MDM2 and evaluated their associations with risk of lung cancer. We found that there were no significant associations between MDM2 SNP309 variant genotypes and lung cancer risk (adjusted OR = 1.20, 95% CI = 0.95β1.53 for TG and adjusted OR = 1.12, 95% CI = 0.85β1.48 for GG, respectively). Similarly, we did not find evidence for any association between risk of lung cancer and MDM2 insertion/deletion polymorphism. The findings suggest that these two MDM2 promoter polymorphisms may not play a major role in lung cancer susceptibility in this Chinese population. Β© 2005 WileyβLiss, Inc.
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