Abstract | OBJECTIVE: METHODS: The case control study has included 200 cases of lung cancer and 200 controls. DNA was extracted from blood samples of all subjects. The genotype of both CYP1A1 and GSTM1 were detected with PCR-based restriction fragment length polymorphisms (PCR-RELP). BPDE-DNA adducts were detected with competitive ELISA. RESULTS:
CYP1A1 mutant genotype and GSTM1 null genotype with smoke has increased the risk of lung cancer, with OR being 2.406(1.321-4.382), 2.755(1.470-5.163), respectively. The level of BPDE-DNA adducts in patients was greater than control, and the adduct level in ever smokers was higher than never smokers, the difference was statistically significant (P= 0.0252). GSTM1 null genotype individuals with BPDE-DNA level higher than 5 adducts/10(8) nucleotide have increased risk of lung cancer (OR= 1.988, 95%CI: 1.011-3.912). Compared with never smokers with CYP1A1 wild genotype, smokers with CYP1A1 mutation genotype had an increased risk of forming a higher level of DNA adducts (P= 0.0459). Smokers with GSTM1 null genotype formed more DNA adducts compared with never smokers with GSTM1 functional genotype (OR = 2.432, 95% CI: 1.072-4.517). CONCLUSION:
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Authors | Chun-mei Chen, Yong-tang Jin, He-yun Xu, Chen-ye Zhang, Hu Zhang, Wei-min Zhang, Cong Tan, Xiao-yu Sun |
Journal | Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
(Zhonghua Yi Xue Yi Chuan Xue Za Zhi)
Vol. 29
Issue 1
Pg. 23-7
(Feb 2012)
ISSN: 1003-9406 [Print] China |
PMID | 22311486
(Publication Type: English Abstract, Journal Article)
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Chemical References |
- Carcinogens
- DNA Adducts
- 7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxide
- CYP1A1 protein, human
- Cytochrome P-450 CYP1A1
- Glutathione Transferase
- glutathione S-transferase M1
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Topics |
- 7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxide
- Carcinogens
- Case-Control Studies
- Cytochrome P-450 CYP1A1
(genetics)
- DNA Adducts
(genetics)
- Female
- Genotype
- Glutathione Transferase
(genetics)
- Humans
- Lung Neoplasms
(chemically induced, enzymology, genetics)
- Male
- Middle Aged
- Polymorphism, Genetic
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