已发表论文

中国汉族人群 TNF  启动子多态性与宫颈癌遗传易感性的关系

 

Authors Yang J, Wang Y, Zhang S, Li Y, Li C, Liu W, Liu S, Liang Y, Zhang X, Yan Z, Shi L, Yao Y 

Received 19 November 2021

Accepted for publication 23 December 2021

Published 10 January 2022 Volume 2022:15 Pages 417—427

DOI https://doi.org/10.2147/IJGM.S350263

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Dr Scott Fraser

Background: The tumour necrosis factor-α (TNF-α ) gene plays an important role in the host immune response, which will influence the development and clearance of cancer. Polymorphism of the TNF-α promoter region is considered to influence its transcription and be a risk factor for tumorigenesis. In the current study, we evaluated the role of TNF-α promoter region polymorphisms in susceptibility to cervical intraepithelial neoplasia (CIN) and cervical cancer (CC).
Methods: A total of 2732 subjects, including 1173 healthy controls, 579 patients with CIN and 980 patients with CC in a Chinese Han population, were selected for the current study. Five SNPs in the TNF-α promoter, rs1799964 (− 1031 C>T), rs1800630 (− 863 A>C), rs1799724 (− 857 C>T), rs1800629 (− 308 A>G) and rs361525 (− 238 A>G), were selected and genotyped using TaqMan Assays. The association of these SNPs with CIN and cervical cancer was evaluated among healthy controls, CIN and CC patients.
Results: The frequency distribution of rs1800629 and rs361525 alleles was significantly different between the CC group and the control group (=0.009 and =0.002). The rs1800629 A allele was found to be a protective factor for CC (OR=0.72; 95% CI=0.56– 0.92). The rs361525 A allele was found to be a risk factor for CC (OR=1.69; 95% CI=1.21– 2.38). After pathological subtyping of CC, the allele distribution of rs1800629 and rs361525 were both significantly different between the cervical squamous cell carcinoma and control groups (P=0.002 and P< 0.001). The rs1800629 A allele was protective factor for cervical squamous cell carcinoma (OR=0.66; 95% CI=0.50– 0.86). The rs361525 A allele was a risk factor for cervical squamous cell carcinoma (OR=1.87; 95% CI=1.32– 2.65). Moreover, the genotypic frequency of rs361525 was significantly different between cervical cancer stage I and stage II (P=0.003).
Conclusion: The rs1800629 and rs361525 in the TNF-α promoter are associated with susceptibility to CC in the Chinese Han population.
Keywords: cervical intraepithelial neoplasia, CIN, cervical cancer, CC, promoter, single-nucleotide polymorphism, SNP, tumour necrosis factor-α, TNF-α