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-308TNF-α 启动子多态性与头颈部鳞状细胞癌患者临床侵袭性的关联。

Association of -308 TNF-α promoter polymorphism with clinical aggressiveness in patients with head and neck squamous cell carcinoma.

机构信息

Health Science Programme, Health Research Laboratory, Department of Dentistry, Universidade Estadual de Montes Claros, 39401-001 Montes Claros, MG, Brazil.

出版信息

Oral Oncol. 2011 Sep;47(9):888-94. doi: 10.1016/j.oraloncology.2011.07.001. Epub 2011 Jul 23.

Abstract

Genetic polymorphisms in the promoter region of the tumour necrosis factor-α (TNF-α) gene are involved in the regulation of the expression levels of its cytokine. Besides, these polymorphisms have been associated with the clinical behaviour of cancer. We investigated the -308 promoter region polymorphisms of the TNF-α gene and its association with the clinicopathological factors of a head and neck squamous cell carcinoma (HNSCC) sample. Furthermore, we analysed the impact of all the variables on the overall survival of patients. A sample of HNSCC (n=89) was evaluated. Clinicopathological factors and overall survival data were gathered. The TNF-α gene was analysed by using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Data analyses were performed by using bivariate and multivariate statistical tests. Significance was set at p<0.05. HNSCC subjects carrying the A allele (GA/AA) exhibited associations with poor performance status (OR=2.82, p=0.039), lesions located on posterior areas (OR=4.02, p=0.002), and large-size tumours (OR=2.91, p=0.015). Subjects carrying only AA genotype exhibited association with poor performance status (OR=6.667, p=0.007). A worse overall survival was noted in subjects with large tumours (OR=4.87, p=0.005) and locoregional metastatic disease (OR=2.50, p=0.018). Our data suggests that the presence of the A allele/AA haplotype in HNSCC individuals might contribute to the higher clinical aggressiveness of malignant disease.

摘要

肿瘤坏死因子-α(TNF-α)基因启动子区域的遗传多态性参与其细胞因子表达水平的调节。此外,这些多态性与癌症的临床行为有关。我们研究了 TNF-α 基因的-308 启动子区域多态性及其与头颈部鳞状细胞癌(HNSCC)样本临床病理因素的关系。此外,我们分析了所有变量对患者总生存的影响。评估了 HNSCC 样本(n=89)。收集了临床病理因素和总生存数据。使用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析 TNF-α 基因。通过双变量和多变量统计检验进行数据分析。显著性设为 p<0.05。携带 A 等位基因(GA/AA)的 HNSCC 患者与较差的一般状况(OR=2.82,p=0.039)、位于后区的病变(OR=4.02,p=0.002)和大肿瘤(OR=2.91,p=0.015)相关。仅携带 AA 基因型的患者与较差的一般状况(OR=6.667,p=0.007)相关。肿瘤较大的患者(OR=4.87,p=0.005)和局部区域转移疾病(OR=2.50,p=0.018)的总生存率较差。我们的数据表明,HNSCC 个体中 A 等位基因/AA 单倍型的存在可能导致恶性疾病的更高临床侵袭性。

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