Alizadeh Negar, Zahedi Hoda, Koopaie Maryam, Fatahzadeh Mahnaz, Mousavi Reza, Kolahdooz Sajad
Department of Oral Medicine, School of Dentistry, Tehran University of Medical Sciences, North Kargar St, P.O.BOX:14395 -433, Tehran, 14399-55991, Iran.
Division of Oral Medicine, Department of Oral Medicine, Rutgers School of Dental Medicine, 110 Bergen Street, Newark, NJ, 07103, USA.
BMC Pulm Med. 2025 Jan 25;25(1):41. doi: 10.1186/s12890-025-03502-6.
Lung cancer (LC), the primary cause for cancer-related death globally is a diverse illness with various characteristics. Saliva is a readily available biofluid and a rich source of miRNA. It can be collected non-invasively as well as transported and stored easily. The process is also reproducible and cost-effective. The aim of this study was to evaluate the salivary expression of microRNAs let-7a-2, miR-221, and miR-20a in saliva and evaluate their efficacy, using multiple logistic regression (MLR) model, in diagnosis of lung cancer.
Samples of saliva were obtained from 40 lung cancer patients (20 lung adenocarcinoma and 20 lung squamous cell carcinoma) and 20 healthy controls. The levels of let-7a-2, miR-221, and miR-20a expression in saliva were assessed by RT-qPCR. Receiver operating characteristic (ROC) curve was utilized to assess the potential significance of miRNAs in saliva for lung cancer diagnosis with the use of multiple logistic regression (MLR), principal component analysis, and machine learning methods.
Diagnostic odds ratio (DOR) of miR-20a in lung adenocarcinoma diagnosis versus healthy control was higher than miR-221, and DOR of miR-221 was higher than let-7a-2. miR-20a demonstrated a higher DOR for small cell lung carcinoma versus healthy control compared to let-7a-2, which in turn exhibited a higher DOR than miR-221. MLR of miR-221, let-7a-2, miR-20a, and smoking habit using main effects led to accuracy of 0.725 (sensitivity: 0.80, specificity: 0.65) and AUC = 0.795 for differentiation of small-cell lung carcinoma from lung adenocarcinoma. Our results showed that MLR based on salivary miRNAs could diagnose LUAD and SCLC from healthy control using main effects and two-way interactions with the accuracy of 0.90 (sensitivity = 0.95 and specificity = 0.85).
A salivary miRNA-based MLR model is a promising diagnostic tool for lung cancer, offering a non-invasive screening option for high-risk asymptomatic individuals.
肺癌(LC)是全球癌症相关死亡的主要原因,是一种具有多种特征的复杂疾病。唾液是一种易于获取的生物流体,也是miRNA的丰富来源。它可以通过非侵入性方式收集,并且易于运输和储存。该过程具有可重复性且成本效益高。本研究的目的是评估唾液中微小RNA let-7a-2、miR-221和miR-20a的表达,并使用多元逻辑回归(MLR)模型评估它们在肺癌诊断中的效能。
从40例肺癌患者(20例肺腺癌和20例肺鳞状细胞癌)和20例健康对照中获取唾液样本。通过RT-qPCR评估唾液中let-7a-2、miR-221和miR-20a的表达水平。利用受试者操作特征(ROC)曲线,通过多元逻辑回归(MLR)、主成分分析和机器学习方法评估唾液中miRNA对肺癌诊断的潜在意义。
miR-20a在肺腺癌诊断中相对于健康对照的诊断比值比(DOR)高于miR-221,miR-221的DOR高于let-7a-2。与健康对照相比,miR-20a在小细胞肺癌诊断中的DOR高于let-7a-2,而let-7a-2的DOR又高于miR-221。使用主效应的miR-221、let-7a-2、miR-20a和吸烟习惯的MLR对区分小细胞肺癌和肺腺癌的准确率为0.725(敏感性:0.80,特异性:0.65),曲线下面积(AUC)=0.795。我们的结果表明,基于唾液miRNA的MLR使用主效应和双向相互作用可以从健康对照中诊断肺腺癌(LUAD)和小细胞肺癌(SCLC),准确率为0.90(敏感性=0.95,特异性=0.85)。
基于唾液miRNA的MLR模型是一种有前景的肺癌诊断工具,为高危无症状个体提供了一种非侵入性筛查选择。