This study demonstrated the association of polymorphisms in (Asp312Asn) rs1799793, (Lys751Gln) rs13181, (Arg399Gln) rs25487 and (Thr241Met) rs861539 polymorphisms with a susceptibility of lung cancer (LC) onset in the Saudi population. The study was performed on 134 LC patients and 270 controls. The data revealed that there was no significant association of LC with subtype squamous cell carcinoma (SCC), small cell lung cancer (SCLC) and adenocarcinoma with the rs1799793 polymorphism. The data showed that the CC genotype for rs13181, the AA genotype for rs25487, and the genotype TT for rs861539 were significantly associated with SCC susceptibility ( < 0.05). Similarly, the CC genotype for rs13181 and the AA genotype for rs25487 were significantly associated with adenocarcinoma susceptibility ( < 0.05). Whereas, the TT genotype for rs861539 was significantly associated with SCLC susceptibility ( = 0.005). In total, significant association of LC susceptibility was found in the following combination models of recessive genotypes: AC heterozygous for rs13181 + AA homozygous for rs25487, CC homozygous for rs13181 + GA heterozygous for rs25487, CC homozygous for rs13181 + AA homozygous for rs25487, CC homozygous for rs13181 + TT homozygous for rs861539, GA heterozygous for rs25487 + CT heterozygous for rs861539, GA heterozygous for rs25487 + TT homozygous for rs861539, AA homozygous for rs25487 + CT heterozygous for rs861539, AA homozygous for rs25487+ TT homozygous for rs861539. These data clearly demonstrated that the combination of recessive genotypes may be associated with susceptibility of LC onset ( < 0.05). In short, the data indicated that DNA repair genes increase LC risk via gene-gene interaction rather than independent variants.
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http://dx.doi.org/10.1080/15257770.2022.2052317 | DOI Listing |
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