Humain genetic lab, Medical school of Tunis, Tunis El Manar University, Tunisia.
Clinical biology lab, Salah Azaiz Institute, Tunisia.
Tunis Med. 2024 Feb 5;102(2):100-106. doi: 10.62438/tunismed.v102i2.4270.
The Toll-like receptor 4 (TLR4), an important member of the host's innate immune response, is coded by a polymorphic gene. This polymorphism could be a predisposing factor for NasoPharyngeal Carcinoma (NPC).
To determine the association between TLR4 gene polymorphisms and the susceptibility to NPC in a cohort of Tunisian affected patients.
Genomic DNAs from 245 unrelated patients affected by undifferentiated carcinoma type (UCNT) and 264 unrelated healthy controls were genotyped for the five single nucleotides polymorphisms (SNPs) of TLR4 locus (4434 A>G (rs1927914),7263 G>C (rs10759932), 6134 A>G(rs4986790), 8851C>T (rs 4986791), 5272 T>C(rs11536889), +8469 T>C (rs11536891)) by Taqman® 5'-nuclease assay.
Among all polymorphisms studied, only the rs4986790 G and rs4986791 T alleles were significantly more prevalent in patients' group than controls (45% vs. 38%; p=0.03; pc=0.06) and increased the risk of the NPC (OR=1.3, 95% CI=1.01-1.69). Also, we found that the frequency of the rs4986790 AA and rs4986791 TT genotypes was significantly higher in controls than in patients (25.7% vs 37%; p=0.006, pc=0.02) and conferred a protector factor in NPC (OR= 0.59, 95% CI= 0.39-0.87). Further, based on the Kaplan-Meier survival curve we observed also the positive effect ofrs1927914 AA genotype on a prognostic of NPC (p=0.006; pc=0.01).
Our study demonstrated that impaired production of TLR4 seems to be a risk factor of NPC development but functional studies are needed to confirm these findings. As to rs1927914 AA appears to be a good biomarker for better survival in a patient with NPC.
Toll 样受体 4(TLR4)是宿主固有免疫反应的重要成员,由多态性基因编码。这种多态性可能是鼻咽癌(NPC)的易感因素。
确定 TLR4 基因多态性与突尼斯患者 NPC 易感性之间的关联。
对 245 名未分化癌型(UCNT)的无关联患者和 264 名无关联健康对照者的基因组 DNA 进行 TLR4 基因座的五个单核苷酸多态性(SNP)(4434A>G(rs1927914)、7263G>C(rs10759932)、6134A>G(rs4986790)、8851C>T(rs4986791)、5272T>C(rs11536889)和 +8469T>C(rs11536891))的 Taqman®5'-核酸酶检测。
在所研究的所有多态性中,只有 rs4986790G 和 rs4986791T 等位基因在患者组中的频率明显高于对照组(45% vs. 38%;p=0.03;pc=0.06),并增加 NPC 的风险(OR=1.3,95%CI=1.01-1.69)。此外,我们发现 rs4986790AA 和 rs4986791TT 基因型在对照组中的频率明显高于患者组(25.7% vs. 37%;p=0.006,pc=0.02),并在 NPC 中发挥保护因子的作用(OR=0.59,95%CI=0.39-0.87)。此外,基于 Kaplan-Meier 生存曲线,我们还观察到 rs1927914AA 基因型对 NPC 预后的积极影响(p=0.006;pc=0.01)。
我们的研究表明,TLR4 产生受损似乎是 NPC 发展的危险因素,但需要功能研究来证实这些发现。至于 rs1927914AA 似乎是 NPC 患者更好生存的良好生物标志物。