Genetic polymorphisms in DNA repair genes and risk of lung cancer

Polymorphisms in DNA repair genes may be associated with differences in the repair efficiency of DNA damage and may influence an individual's risk of lung cancer. The frequencies of several amino acid substitutions in XRCC1 ( Arg194Trp, Arg280His and Arg399Gln), XRCC3 (Thr241Met), XPD (Ilel99Met, His a201Tyr, Asp312Asn and Lys751Gln) and XPF (Pro379Ser) genes were studied in 96 non-small-cell lung cancer (NSCLC) cases and in 96 healthy controls mat ched for age, gender and cigarette smoking. The XPD codon 312 Asp/Asp genot ype was found to have almost twice the risk of lung cancer when the Asp/Asn + Asn/Asn combined genotype served as reference [odds ratio (OR) 1.86, 95% confidence interval (CI), 1.02-3.40]. In light cigarette smokers (less tha n the median of 34.5 pack-years), the XPD codon 312 Asp/Asp genotype was mo re frequent among cases than in controls and was associated with an increas ed risk of NSCLC, Compared with the Asn/ Asn carriers, the OR in light smok ers with the Asp/Asn genotype was 1.70 (CI0.35 0.43-6.74) and the OR in tho se with the Asp/Asp genotype was 5.32 (CI0.35-21.02) (P trend = 0.01), The 312 Asp/Asp genotype was not associated with lung cancer risk in never-smok ers or heavy smokers (>34.5 pack-years). The XPD-312Asp and -751Lys polymor phisms were in linkage disequilibrium in the group studied; this finding wa s further supported by pedigree analysis of four families from Utah. The XP D 312Asp amino acid is evolutionarily conserved and is located in the seven -moth helicase domain of the RecQ family of DNA helicases, Our results indi cate that these polymorphisms in the XPD gene should be investigated furthe r for the possible attenuation of DNA repair and apoptotic functions and th at additional molecular epidemiological studies are warranted to extend the se findings.