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- W2023459786 abstract "Abstract Polymorphisms at N ‐acetyl transferase 2 locus ( NAT2 ) lead to slow, intermediate and rapid acetylation properties of the enzyme. Improper acetylation of heterocyclic and aromatic amines, present in tobacco, might cause DNA adduct formation. Generally, DNA repair enzymes remove these adduct to escape malignancy. But, tobacco users carrying susceptible NAT 2 and DNA repair loci might be at risk of oral leukoplakia and cancer. In this study, 389 controls, 224 leukoplakia and 310 cancer patients were genotyped at 5 polymorphic sites on NAT2 and 3 polymorphic sites on each of XRCC1 and XPD loci by PCR‐RFLP method to determine the risk of the diseases. None of the SNPs on these loci independently could modify the risk of the diseases in overall population but variant genotype ( Gln/Gln ) at codon 399 on XRCC1 and major genotype ( Lys/Lys ) at codon 751 on XPD were associated with increased risk of leukoplakia and cancer among slow acetylators, respectively (OR = 4.2, 95% CI = 1.2–15.0; OR = 1.6, 95% CI = 1.1–2.3, respectively). Variant genotype ( Asn/Asn ) at codon 312 on XPD was also associated with increased risk of cancer among rapid and intermediate acetylators (OR = 1.9, 95% CI = 1.2–2.9). Variant C‐G‐A haplotype at XRCC1 was associated with increased risk of leukoplakia (OR = 1.7, 95% CI = 1.2–2.4) but leukoplakia and cancer in mixed tobacco users (OR = 3.1, 95% CI = 1.4–7.1, OR = 2.4, 95% CI = 1.1–5.4, respectively) among slow acetylators. Although none of the 3 loci could modulate the risk of the diseases independently but 2 loci in combination, working in 2 different biochemical pathways, could do so in these patient populations. © 2007 Wiley‐Liss, Inc." @default.
- W2023459786 created "2016-06-24" @default.
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- W2023459786 date "2007-03-23" @default.
- W2023459786 modified "2023-10-13" @default.
- W2023459786 title "Polymorphisms at <i>XPD</i> and <i>XRCC1</i> DNA repair loci and increased risk of oral leukoplakia and cancer among <i>NAT2</i> slow acetylators" @default.
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- W2023459786 doi "https://doi.org/10.1002/ijc.22547" @default.
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