1 Whole-Genome Research Core Laboratory of Human Diseases, Chang Gung Memorial Hospital, Keelung, Taiwan.
2 Department of Dermatology, Drug Hypersensitivity Clinical and Research Center, Chang Gung Memorial Hospital, Taipei, Linkou and Keelung, Taiwan.
J Dent Res. 2018 Jun;97(6):717-724. doi: 10.1177/0022034517749451. Epub 2018 Jan 3.
Genetic and acquired factors are thought to be interrelated and imperative to estimate the risk and prognosis of oral squamous cell carcinoma (OSCC). HOX transcript antisense intergenic RNA ( HOTAIR) plays crucial roles in gene regulation and is regulated in a variety of cancers. Polymorphisms in HOTAIR have been recently linked to the predisposition to diverse malignancies. In the present study, we aimed to evaluate the influences of HOTAIR gene polymorphisms, combined with environmental triggers, on the susceptibility to oral tumorigenesis. Four single-nucleotide polymorphisms of the HOTAIR gene- rs920778, rs1899663, rs4759314, and rs12427129-were tested in 1,200 control participants and 907 patients with OSCC. We detected a significant association of rs1899663 with the risk of OSCC (adjusted odds ratio, 2.227; 95% confidence interval [95% CI], 1.197 to 4.146; P = 0.012) after adjustment for 3 potential confounders: smoking, betel quid chewing, and alcohol consumption. In further analyses where habitual exposure to each of 3 environmental factors was excluded, we found that, in addition to rs1899663, non-betel quid users who carried the polymorphic allele of rs920778 were more prone to develop OSCC than were those homozygous for wild-type allele (TC: odds ratio [OR], 1.472; 95% CI, 1.069 to 2.029; P = 0.018; TC+CC: OR, 1.448; 95% CI, 1.060 to 1.977; P = 0.020). Moreover, in exploring the relationship between HOTAIR gene polymorphisms and the clinical status of only patients with OSCC who were non-betel quid chewers (excluding the advanced clinical stage), we found that rs920778 and rs4759314 were correlated with the development of large-size tumors (OR, 1.891; 95% CI, 1.027 to 3.484; P = 0.04) and increased lymph node metastasis (OR, 4.140; 95% CI, 1.785 to 9.602; P = 0.001), respectively. Further functional assessments link rs920778 to the regulation of HOTAIR expression and epigenetic status. Our results reveal an interactive effect of HOTAIR gene polymorphisms and betel quid chewing on the development and progression of oral cancer.
遗传和获得性因素被认为是相互关联的,对于评估口腔鳞状细胞癌(OSCC)的风险和预后至关重要。HOX 转录反义基因间 RNA(HOTAIR)在基因调控中发挥着关键作用,并且在多种癌症中受到调控。HOTAIR 的多态性最近与多种恶性肿瘤的易感性有关。在本研究中,我们旨在评估 HOTAIR 基因多态性与环境触发因素共同作用对口腔肿瘤发生易感性的影响。在 1200 名对照参与者和 907 名 OSCC 患者中检测了 HOTAIR 基因的四个单核苷酸多态性-rs920778、rs1899663、rs4759314 和 rs12427129。在调整了 3 个潜在混杂因素(吸烟、嚼槟榔和饮酒)后,我们发现 rs1899663 与 OSCC 风险显著相关(调整后的优势比,2.227;95%置信区间[95%CI],1.197 至 4.146;P=0.012)。在进一步排除了 3 个环境因素的习惯性暴露的分析中,我们发现除了 rs1899663 之外,携带 rs920778 多态性等位基因的非嚼槟榔者比携带野生型等位基因的个体更容易发生 OSCC(TC:比值比[OR],1.472;95%CI,1.069 至 2.029;P=0.018;TC+CC:OR,1.448;95%CI,1.060 至 1.977;P=0.020)。此外,在仅对非嚼槟榔的 OSCC 患者(排除晚期临床阶段)的临床状况进行 HOTAIR 基因多态性与关系的探讨时,我们发现 rs920778 和 rs4759314 与大尺寸肿瘤的发展相关(OR,1.891;95%CI,1.027 至 3.484;P=0.04)和增加的淋巴结转移(OR,4.140;95%CI,1.785 至 9.602;P=0.001)。进一步的功能评估将 rs920778 与 HOTAIR 表达和表观遗传状态的调节联系起来。我们的结果揭示了 HOTAIR 基因多态性和嚼槟榔与口腔癌的发展和进展之间的相互作用。