TNFAIP8L1 and FLT1 polymorphisms alter the susceptibility to cervical cancer amongst uyghur females in China

Aims: TNFAIP8L1 and FLT1 play critical roles in the occurrence and development of tumors, but no in-depth studies have been carried out in cervical cancer. This study aims to research the correlation between polymorphisms of these two genes and the risk of cervical cancer in the Uygur women. Methods: The study involved 342 cervical cancer patients and 498 healthy women. Five SNPs from the TNFAIP8L1 gene and the FLT1 gene were selected and genotyped. Odds ratio (ORs) and 95% confidence intervals (95% CIs) were calculated by logistic regression analysis to evaluate the correlation between SNPs and cervical cancer risk. Results: The alleles rs9917028-A ( p = 0.032), rs10426502-A ( p = 0.007) and rs1060555-G ( p = 0.026) of TNFAIP8L1 were associated with a decreased risk of cervical cancer. In the multiple genetic models, these three SNPs were also associated with the risk of cervical cancer. The stratified analysis showed that TNFAIP8L1 -rs10426502, -rs1060555 and FLT1 -rs9513111 were associated with a decreased risk of cervical cancer among people older than 43 years. Moreover, the haplotypes AG ( p = 0.007) and GC ( p = 0.026) of linkage disequilibrium (LD) block rs10426502|rs1060555 in TNFAIP8L1 were significantly associated with an increased risk of cervical cancer. Conclusions: Our results suggested that the relationships between TNFAIP8L1 and FLT1 polymorphisms and the risk of cervical cancer among Uyghur females.