Department of Orthodontics, School of Dentistry, Kermanshah University of Medical Sciences, Kermanshah 6713954658, Iran.
Medical Biology Research Centre, Kermanshah University of Medical Sciences, Kermanshah 6714415185, Iran.
Medicina (Kaunas). 2024 Mar 14;60(3):478. doi: 10.3390/medicina60030478.
: Nucleotide Excision Repair (NER), the most extensively researched DNA repair mechanism, is responsible for repairing a variety of DNA damages, and Xeroderma Pigmentosum (XP) genes participate in NER. Herein, we aimed to update the previous results with a meta-analysis evaluating the association of XPA, XPB/ERCC3, XPF/ERCC4, and XPG/ERCC5 polymorphisms with the susceptibility to HNC. : PubMed/Medline, Web of Science, Scopus, and Cochrane Library databases were searched without any restrictions until 18 November 2023 to find relevant studies. The Review Manager 5.3 (RevMan 5.3) software was utilized to compute the effect sizes, which were expressed as the odds ratio (OR) with a 95% confidence interval (CI). : Nineteen articles were involved in the systematic review and meta-analysis that included thirty-nine studies involving ten polymorphisms. The results reported that the CC genotype of polymorphism showed a significantly decreased risk of HNC in the recessive model (OR: 0.89; 95%CI: 0.81, 0.99; -value is 0.03). In addition, the CT genotype (OR: 0.65; 95%CI: 0.48, 0.89; -value is 0.008) of the polymorphism was associated with a decreased risk, and the T allele (OR: 1.28; 95%CI: 1.05, 1.57; -value is 0.02), the TT (OR: 1.74; 95%CI: 1.10, 2.74; -value is 0.02), and the TT + CT (OR: 2.22; 95%CI: 1.04, 4.74; -value is 0.04) genotypes were associated with an increased risk of HNC. : The analysis identified two polymorphisms, and , as being significantly associated with the risk of HNC. The study underscored the influence of various factors, such as the type of cancer, ethnicity, source of control, and sample size on these associations.
核苷酸切除修复(NER)是研究最为广泛的 DNA 修复机制,负责修复多种 DNA 损伤,而着色性干皮病(XP)基因参与 NER。在此,我们旨在通过荟萃分析来更新之前的结果,评估 XPA、XPB/ERCC3、XPF/ERCC4 和 XPG/ERCC5 多态性与头颈部癌症(HNC)易感性的相关性。
我们在 2023 年 11 月 18 日之前,无限制地检索了 PubMed/Medline、Web of Science、Scopus 和 Cochrane Library 数据库,以查找相关研究。使用 Review Manager 5.3(RevMan 5.3)软件计算效应大小,结果表示为比值比(OR)和 95%置信区间(CI)。
该系统评价和荟萃分析共纳入 19 篇文章和 39 项研究,涉及 10 种多态性。结果表明, 多态性的 CC 基因型在隐性模型中显著降低了 HNC 的风险(OR:0.89;95%CI:0.81,0.99;-值为 0.03)。此外, 多态性的 CT 基因型(OR:0.65;95%CI:0.48,0.89;-值为 0.008)与降低风险相关,T 等位基因(OR:1.28;95%CI:1.05,1.57;-值为 0.02)、TT(OR:1.74;95%CI:1.10,2.74;-值为 0.02)和 TT + CT(OR:2.22;95%CI:1.04,4.74;-值为 0.04)基因型与 HNC 风险增加相关。
该分析确定了两个多态性 和 与 HNC 风险显著相关。该研究强调了各种因素(如癌症类型、种族、对照来源和样本量)对这些关联的影响。