TLR9 和 TLR7 基因多态性对口腔鳞状细胞癌患者预后和生存期的影响。

0 MEDICINE, RESEARCH & EXPERIMENTAL
Miroslav Obrenović, Gordana Šupić, Satoru Miyabe, Irena Mladenović, Ružica Kozomara, Saša Jović, Aleksandra Petković Ćurčin, Debora Štefik, Srboljub Stosić, Biserka Vukomanović Đurđević
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引用次数: 0

摘要

尽管人们在开发新的诊断和治疗方法方面做出了巨大努力,但口腔鳞状细胞癌(OSCC)的复发率仍然很高,五年生存率很低,而且发病率越来越高。Toll样受体(TLRs)在激活后启动并延续免疫机制,它与免疫监视和抗肿瘤免疫反应有关。本研究旨在调查 TLR7 rs3853839 和 TLR9 rs187084 基因的多态性与 OSCC 风险、临床病理特征和存活率之间的关联。通过实时聚合酶链反应(PCR)对 95 例 HPV 阴性 OSCC 患者和 107 例年龄和性别匹配的健康对照者进行了基因分型评估。与主要 TT 基因型(P = 0.020)和 T-等位基因携带者(TT + CT 基因型组合,P = 0.015)相比,淋巴结转移患者的 TLR9 rs187084 CC 变异基因型频率更高。与 TT(P = 0.047)和 T-等位基因携带者(TT + CT,P = 0.037)相比,TLR9 rs187084 变异 CC 基因型患者的晚期 III 期发病率更高。卡普兰-梅耶尔分析显示,与TT基因型(P = 0.010,对数秩检验)和T-等位基因携带者(TT + CT,P = 0.002)相比,TLR9 rs187084变异CC基因型患者的总生存率较低,但这并不是总生存率的独立预测因素。TLR9 rs187084和TLR7 rs3853839多态性均与大量饮酒有关(P = 0.027和P = 0.001)。所研究的基因变异与 OSCC 易感性无关。TLR9 rs187084多态性的变异CC基因型可能是OSCC生存率低和肿瘤进展的标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of TLR9 and TLR7 gene polymorphisms on prognosis and survival of patients with oral squamous cell carcinoma.

Despite significant efforts in developing new diagnostic and therapeutic modalities, oral squamous cell carcinomas (OSCCs) still exhibit a high recurrence rate, a low five-year survival rate, and an increasing prevalence. Toll-like receptors (TLRs), which initiate and perpetuate immune mechanisms upon activation, have been linked to immune surveillance and the antitumor immune response. The aim of this study was to investigate the association between the polymorphisms of the TLR7 rs3853839 and TLR9 rs187084 genes and OSCC risk, clinicopathological features, and survival. Genotyping was assessed by real-time polymerase chain reaction (PCR) in 95 HPV negative OSCC patients and 107 age- and sex-matched healthy controls. Patients with lymph node metastases had higher frequencies of the TLR9 rs187084 CC variant genotype compared to the major TT genotype (P = 0.020) and to T-allele carriers (combined TT + CT genotypes, P = 0.015). A higher prevalence of advanced stage III was observed in patients with the TLR9 rs187084 variant CC genotype compared to TT (P = 0.047) and to T-allele carriers (TT + CT, P = 0.037). Kaplan-Meier analysis revealed a lower overall survival (OS) rate in patients with the TLR9 rs187084 variant CC genotype compared to the TT genotype (P = 0.010, log-rank test) and to T-allele carriers (TT + CT genotypes, P = 0.002), though it was not an independent predictor of OS. Both TLR9 rs187084 and TLR7 rs3853839 polymorphisms were associated with high alcohol consumption (P = 0.027 and P = 0.001, respectively). The investigated genetic variations were not associated with OSCC susceptibility. The variant CC genotype of the TLR9 rs187084 polymorphism might be a marker of poor survival and tumor progression in OSCC.

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