Department of Oncology, Krishna Vishwa Vidyapeeth "Deemed to be University", Taluka-Karad, Dist- Satara, Maharashtra) India.
Department of Molecular Biology & Genetics, Krishna Vishwa Vidyapeeth "Deemed to be University", Taluka-Karad, Dist- Satara,Maharashtra, India.
Asian Pac J Cancer Prev. 2024 Jan 1;25(1):191-199. doi: 10.31557/APJCP.2024.25.1.191.
The present study was planned to investigate possible association of single nucleotide polymorphisms (SNPs) of nucleotide excision repair (NER) genes such as XPC, XPD, XPG with acute radiation induced toxicities such as skin reactions and oral mucositis in normal tissue from head and neck cancer (HNC) patients receiving radiotherapy. Methods: Two hundred and fifty HNC patients receiving radiotherapy were enrolled in this study and the acute toxicity reactions and radiation response were recorded. Association of SNPs rs2228001 of XPC, rs238406, rs13181 of XPD and rs17655 of XPG gene with normal tissue reactions in the form of dermatitis and mucositis were studied by PCR-RFLP and direct DNA sequencing.
The results of univariate analysis of SNPs of XPC, XPD and XPG showed that XPC polymorphism at codon 939 of exon 15 (A>C) was not associated with dermatitis (OR=0.30, 95% CI: 0.06-1.39; p=0.125), or oral mucositis (OR=1.14, 95% CI: 0.41-3.20; p=0.793). The XPD codon 156 of exon 6 (C>A) and codon 751 of exon-23 A>C) polymorphism showed no association with radiosensitivity in HNC patients (OR=1.50, 95% CI: 0.60-3.71; p=0.080) for dermatitis, (OR=1.54, 95% CI: 0.66-3.61; p=0.312) for oral mucositis. The 1104 Asp variant genotype or allele of XPG (OR=1.35 95% CI: 0.50-3.64; p=0.541) showed no association with degree of radiotherapy associated dermatitis or mucositis (OR=0.80, 95% CI: 0.32-2.03; p=0.648) in HNC patients. The variant C allele of 2920 A/C genotype of XPC gene at codon 939 of exon 15, found protective with developing skin reactions with grade >1 (OR=0.60, 95% CI: 0.36-0.97; p=0.039) in HNC patients treated with radiotherapy.
The results obtained in this study concluded that the SNPs rs2228001of XPC, rs238406, rs13181 SNPs of XPD and rs17655 SNP of XPG are not associated with normal tissue toxicity in HNC patients treated with radiotherapy. Radiotherapy with high radiation dose was significantly associated with oral mucositis in response to radiotherapy.
本研究旨在探讨核苷酸切除修复(NER)基因如 XPC、XPD、XPG 的单核苷酸多态性(SNPs)与头颈部癌症(HNC)患者接受放疗后正常组织的急性辐射诱导毒性(如皮肤反应和口腔粘膜炎)之间可能存在的关联。方法:本研究纳入了 250 名接受放疗的 HNC 患者,并记录了急性毒性反应和放射反应。通过 PCR-RFLP 和直接 DNA 测序研究 XPC 基因 rs2228001、XPD 基因 rs238406、rs13181 和 XPG 基因 rs17655 与皮肤炎和粘膜炎形式的正常组织反应的 SNP 相关性。结果:XPC、XPD 和 XPG 基因 SNP 的单变量分析结果表明,外显子 15 密码子 939 处的 XPC 多态性(A>C)与皮肤炎(OR=0.30,95%CI:0.06-1.39;p=0.125)或口腔粘膜炎(OR=1.14,95%CI:0.41-3.20;p=0.793)无关。XPD 外显子 6 密码子 156(C>A)和外显子 23 密码子 751(A>C)多态性与 HNC 患者的放射敏感性无关(皮肤炎的 OR=1.50,95%CI:0.60-3.71;p=0.080),(口腔粘膜炎的 OR=1.54,95%CI:0.66-3.61;p=0.312)。XPG 基因 1104 位天冬氨酸变体基因型或等位基因(OR=1.35,95%CI:0.50-3.64;p=0.541)与 HNC 患者放射治疗相关皮肤炎或粘膜炎的严重程度无关(OR=0.80,95%CI:0.32-2.03;p=0.648)。XPC 基因外显子 15 密码子 939 处 2920A/C 基因型的变体 C 等位基因与皮肤反应(OR=0.60,95%CI:0.36-0.97;p=0.039)有关,在接受放疗的 HNC 患者中,这种变体与 >1 级的皮肤反应有关。结论:本研究结果表明,XPC 的 rs2228001、rs238406、rs13181 以及 XPG 的 rs17655 SNP 与接受放疗的 HNC 患者的正常组织毒性无关。高放射剂量的放疗与口腔粘膜炎的放射反应显著相关。