Cheng Yi-Shing Lisa, Jordan Lee, Rees Terry, Chen Huey-Shys, Oxford Lance, Brinkmann Ole, Wong David
Department of Diagnostic Sciences, Texas A&M University-Baylor College of Dentistry, 3302 Gaston Ave, Dallas, TX, USA,
Clin Oral Investig. 2014 Apr;18(3):985-93. doi: 10.1007/s00784-013-1041-0. Epub 2013 Jul 28.
To gather preliminary data concerning the feasibility of using seven salivary mRNAs-IL-8; IL-1β; dual specificity phosphatase 1 (DUSP1); H3 histone family 3A (H3F3A); ornithin decarboxylase antizyme 1 (OAZ1); S100 calcium-binding protein P (S100P); and spermidine/spermine N1-acetyltransferase 1 (SAT1)-for detecting development of oral squamous cell carcinoma (OSCC) in oral lichen planus (OLP) patients and OSCC patients whose disease was in remission.
Saliva samples were collected from five study groups (25 subjects/group): newly diagnosed OSCC, OSCC-in-remission, disease-active OLP, disease-inactive OLP, and normal controls. The salivary mRNA levels were determined by a pre-amplification RT-qPCR approach with nested gene-specific primers. Mean fold changes between each pair of study groups were analyzed by the Mann-Whitney U test.
Salivary levels of OAZ1, S100P, and DUSP1 mRNAs were significantly higher in newly diagnosed OSCC patients, compared to: (1) normal controls (p = 0.003; p = 0.003; and p < 0.001, respectively); (2) OSCC-in-remission (p < 0.001; p = 0.001; and p < 0.001, respectively); (3) disease-active OLP (p < 0.001; p = 0.016; and p < 0.001, respectively); and (4) disease-inactive OLP (p = 0.043; p < 0.001; and p < 0.001, respectively). No significant differences were found in the levels of salivary IL-8, IL-1β, H3F3A, and SAT1 mRNAs between newly diagnosed OSCC patients and the normal controls (p = 0.093, 0.327, 0.764, and 0.560, respectively).
Salivary OAZ1, S100P, and DUSP1 mRNAs are candidate biomarkers for detecting OSCC development in OSCC patients in remission and in OLP patients.
The results of this study serve as the basis for a further large-scale study which may lead to a non-invasive screening method for early detection of OSCC.
收集关于使用七种唾液mRNA(白细胞介素-8;白细胞介素-1β;双特异性磷酸酶1(DUSP1);H3组蛋白家族3A(H3F3A);鸟氨酸脱羧酶抗酶1(OAZ1);S100钙结合蛋白P(S100P);以及亚精胺/精胺N1-乙酰转移酶1(SAT1))检测口腔扁平苔藓(OLP)患者和疾病缓解期口腔鳞状细胞癌(OSCC)患者口腔鳞状细胞癌发生情况的初步数据。
从五个研究组(每组25名受试者)收集唾液样本:新诊断的OSCC、缓解期OSCC、疾病活动期OLP、疾病非活动期OLP和正常对照。采用带有巢式基因特异性引物的预扩增逆转录定量聚合酶链反应(RT-qPCR)方法测定唾液mRNA水平。通过曼-惠特尼U检验分析每对研究组之间的平均倍数变化。
与以下相比,新诊断的OSCC患者唾液中OAZ1、S100P和DUSP1 mRNA水平显著更高:(1)正常对照(分别为p = 0.003;p = 0.003;p < 0.001);(2)缓解期OSCC(分别为p < 0.001;p = 0.001;p < 0.001);(3)疾病活动期OLP(分别为p < 0.001;p = 0.016;p < 0.001);以及(4)疾病非活动期OLP(分别为p = 0.043;p < 0.001;p < 0.001)。新诊断的OSCC患者与正常对照之间唾液中白细胞介素-8、白细胞介素-1β、H3F3A和SAT1 mRNA水平未发现显著差异(分别为p = 0.093、0.327、0.764和0.560)。
唾液OAZ1、S100P和DUSP1 mRNA是检测缓解期OSCC患者和OLP患者OSCC发生的候选生物标志物。
本研究结果为进一步的大规模研究奠定了基础,该研究可能会产生一种用于早期检测OSCC的非侵入性筛查方法。