Department of Stomatology, Suzhou Health College, Suzhou, Jiangsu, China.
Oral Dis. 2010 Apr;16(3):299-304. doi: 10.1111/j.1601-0825.2009.01645.x.
To explore a potential causal contribution of the transcription factor HIF-1alpha and its target gene, RTP801 and VEGF, to the development of oral lichen planus (OLP). Design relevant: Twenty-two adult OLP patients were enrolled in this study. All OLP diagnoses were verified by histopathological characteristics. Normal mucous specimens were collected from 12 controls after various oral surgeries.
RNA was isolated from OLP and control specimens. Microarray was performed using BiostarH-40s gene chip. Expression of HIF-1alpha, VEGF and RTP801 was evaluated using quantitative real-time polymerase chain reaction (qPCR). Unpaired t-test and one-way ANOVA was used for statistical analysis.
Microarray results showed that RTP801 expression was lower in OLP than in controls (779 vs 3090). qPCR further confirmed that expression of RTP801 was similarly lower in OLP than in controls (0.363 vs 1.473, P < 0.001); expression of VEGF was also lower in OLP (0.448 vs 1.74, P = 0.012). In contrast, expression of HIF-1alpha was higher in OLP than in controls (11.12 vs 1.628, P < 0.001).
The oral mucosa of OLP is hypoxic. Genes that are activated by hypoxia, such as RTP801 and VEGF, and their signal cascades may be novel potential therapeutic targets for OLP.
探索转录因子 HIF-1alpha 及其靶基因 RTP801 和 VEGF 是否对口腔扁平苔藓(OLP)的发生有潜在的因果贡献。设计相关:本研究纳入了 22 名成人 OLP 患者。所有 OLP 诊断均通过组织病理学特征证实。12 名接受各种口腔手术后的对照者采集正常黏膜标本。材料和方法:从 OLP 和对照标本中分离 RNA。使用 BiostarH-40s 基因芯片进行微阵列分析。使用定量实时聚合酶链反应(qPCR)评估 HIF-1alpha、VEGF 和 RTP801 的表达。采用非配对 t 检验和单因素方差分析进行统计学分析。结果:微阵列结果显示,与对照组相比,OLP 中 RTP801 的表达较低(779 比 3090)。qPCR 进一步证实,OLP 中 RTP801 的表达也明显低于对照组(0.363 比 1.473,P<0.001);OLP 中 VEGF 的表达也较低(0.448 比 1.74,P=0.012)。相比之下,OLP 中 HIF-1alpha 的表达高于对照组(11.12 比 1.628,P<0.001)。结论:OLP 的口腔黏膜呈缺氧状态。缺氧激活的基因,如 RTP801 和 VEGF 及其信号通路可能是 OLP 的新的潜在治疗靶点。