AI Summary & Key Takeaways
AI InsightG-carriers were also more likely to have poorer survival compared to patients with CC genotype (p=0.04).Our results suggest that the Codon 72 polymorphism was not associated with the EC in eastern Turkey.
📌 3 Key Takeaways
Özet
The tumor suppressor TP53 gene plays a key role in the regulation of cell cycle. Polymorphisms in this gene have beenassociated with many cancers including esophageal cancer (EC). Many studies in other populations have demonstrated thatcodon 72 polymorphism of TP53 gene contribute to the prediction of EC risk, especially in Asians. The aim of this studywas to explore the effect of codon 72 polymorphism on the EC risk in eastern Turkey.The codon 72 polymorphism was genotyped by real time polymerase chain reaction (qPCR) with TaqMan SNP geno typingassay in 79 patients and 80 healthy control subjects.No statistically significant difference was observed in distribution of genotype and allele frequencies. HeterozygousArg/Pro (CG) was the most frequent genotype in both patients and controls. Homozygous Arg/Arg (GG) genotypefrequency was higher in patients than controls, but not statistically signific ant (p>0.05). However, tumor location in thelower part of the esophagus was significantly higher in non-C carriers (GG, Arg/Arg) compared to C-carriers (CG/CC)(p=0.01). G-carriers were also more likely to have poorer survival compared to patients with CC genotype (p=0.04).Our results suggest that the Codon 72 polymorphism was not associated with the EC in eastern Turkey. However, GGgenotype (Arg/Arg) may have a role in tumor development at the lower location of the esophagus. Additionally, G carriersmay exist the poorer survival compared to the non-G carriers (CC). Therefore, it is thought that individuals with CCgenotype (Pro/Pro) may have better survival.