CYP1A1 gene polymorphisms and smoking status as modifier factors for lung cancer risk

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• 作者：Atef G. Hussein^a ; Heba F. Pasha^a ; ^{hebapasha@yahoo.com" class="auth_mail} ; Hanan M. El-Shahat^b ; Doaa M. Gad^b ; Mostafa M. Toam^c
• 关键词：CYP ; cytochrome P450 ; SIM ; measures in additive (SI) and multiplicative models ; RERI ; relative excess risk due to interaction ; AP ; attributable proportion of the disease due to interaction ; AD (56.4%) ; adenocarcinoma ; SCC ; squamous cell carcinoma ; PAH ; polycyclic aromatic hydrocarbons ; AHH ; aryl hydrocarbon hydroxylase
• 刊名：Gene
• 出版年：10 May, 2014
• 年：2014
• 卷：541
• 期：1
• 页码：26-30
• 全文大小：248 K

文摘

Objective

Lung cancer remains the most prevalent malignancy worldwide. Susceptibility to lung cancer has been shown to be modulated by inheritance of polymorphic genes. Several metabolic enzymes are currently under investigation for their possible role in lung cancer susceptibility, including members of the cytochrome P450 (CYP) superfamily. The aim of this work was to identify the correlation between CYP1A1 m1 and m2 polymorphisms and lung cancer risk and figure its interactions with smoking as genetic modifiers in the etiology of lung cancer in the Egyptian population.

Materials and methods

One hundred and ten patients with lung cancer and one hundred and ten controls were enrolled in the study. CYP1A1 m1 and m2 polymorphisms were determined using polymerase chain reaction restriction fragment length polymorphism.

Results

Subjects carrying TC and CC genotypes of CYP1A1 m1 and AG and GG genotypes of CYP1A1 m2 were significantly more likely to develop lung cancer especially squamous cell carcinoma. The proportion of lung cancer attributable to the interaction of smoking and CYP1A1 m1 and CYP1A1 m2 polymorphisms was 32% and 52% respectively.

Conclusion

Our results revealed that CYP1A1 m1 and m2 polymorphisms contribute to smoking related lung cancer risk in the Egyptian population.