Abstract

Objective To investigate the association between genetic polymorphism in exon 26 C3435T and exon 21 G2677T/A of the multidrug resistance 1 (MDR1) gene and the sporadic colorectal adenocarcinoma.Methods A total of 123 patients with colorectal adenocarcinoma and 86 healthy subjects as controls were included.Snapshot SNP typing was used to determine the allele and genotype frequencies of MDR1 C3435T,and G2677T/A.Results There was no significant difference in the distribution of MDR1 C3435T and G2677T/A alleles and genotypes frequencies between control group and case group.When stratified by clinicopathological features such as lesion distribution,differentiation degree and Duke' s stage in the patients with colorectal adenocarcinoma,the statistically significant differences were found in the frequency of C3435T genotype between patients with colon adenocarcinoma (CC 22.2%,CT 63.4%,and TT 14.8 %) and rectal adenocarcinoma (CC 50.7%,CT 31.9%,and TT 17.4%) (P < 0.01).The frequency of 3435T allele was decreased significantly in patiens with rectal adenocarcinoma (33.3%) as compared with colon adenocarcinoma (46.3%,P <0.05).And the frequency of 2677GT genotype was decreased significantly in patients with moderately-differentiated (26.9%) as compared with well-differentiated (46.4%) and poorly-differentiated (47.1%,P < 0.05).Furthermore,the frequency of 2677GT genotype was increased significantly in patients with colon adenocarcinoma (46.3%) as compared with rectal adenocarcinoma (24.6%,P < 0.05),and the frequency of 2677G allele was decreased significantly in patiens with poorly differentiated adenocarcinoma (3.7%) as compared with moderately-differentiated (28.5%) and well-differentiated adenocarcinoma (11.0%,P < 0.05).Conclusion MDR1 C3435T and G2677T/A polymorphisms were found to be not associated with colorectal adenocarcinoma. Key words: Colorectal carcinoma; Multidrug resistance gene; Polymorphism

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