A prediction model for distinguishing lung squamous cell carcinoma from adenocarcinoma

被引:18
|
作者
Li, Hui [1 ]
Jiang, Zhengran [2 ,3 ]
Leng, Qixin [2 ]
Bai, Fan [1 ]
Wang, Juan [4 ]
Ding, Xiaosong [1 ]
Li, Yuehong [4 ]
Zhang, Xianghong [1 ,4 ]
Fang, HongBin [5 ]
Yfantis, Harris G. [6 ]
Xing, Lingxiao [1 ]
Jiang, Feng [2 ]
机构
[1] Hebei Med Univ, Dept Pathol, Shijiazhuang, Hebei, Peoples R China
[2] Univ Maryland, Sch Med, Dept Pathol, Baltimore, MD 21201 USA
[3] Uniformed Serv Univ Hlth Sci, F Edward Hebert Sch Med, Bethesda, MD 20814 USA
[4] Hebei Med Univ, Hosp 2, Dept Pathol, Shijiazhuang, Hebei, Peoples R China
[5] Georgetown Univ, Med Ctr, Dept Biostat Bioinformat & Biomath, Washington, DC 20007 USA
[6] Baltimore Vet Affairs Med Ctr, Pathol & Lab Med, Baltimore, MD USA
基金
中国国家自然科学基金;
关键词
MiRNA; biomarkers; lung cancer; histology; cytology; IN-SITU HYBRIDIZATION; CANCER DIAGNOSIS; COMPUTED-TOMOGRAPHY; BRONCHOALVEOLAR LAVAGE; MICRORNA BIOMARKERS; PULMONARY NODULES; SPUTUM; SPECIMENS; MARKERS; CLASSIFICATION;
D O I
10.18632/oncotarget.17038
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Accurate classification of squamous cell carcinoma (SCC) from adenocarcinoma (AC) of non-small cell lung cancer (NSCLC) can lead to personalized treatments of lung cancer. We aimed to develop a miRNA-based prediction model for differentiating SCC from AC in surgical resected tissues and bronchoalveolar lavage (BAL) samples. Expression levels of seven histological subtype-associated miRNAs were determined in 128 snap-frozen surgical lung tumor specimens by using reverse transcription-polymerase chain reaction (RT-PCR) to develop an optimal panel of miRNAs for acutely distinguishing SCC from AC. The biomarkers were validated in an independent cohort of 112 FFPE lung tumor tissues, and a cohort of 127 BAL specimens by using droplet digital PCR for differentiating SCC from AC. A prediction model with two miRNAs (miRs-205-5p and 944) was developed that had 0.988 area under the curve (AUC) with 96.55% sensitivity and 96.43% specificity for differentiating SCC from AC in frozen tissues, and 0.997 AUC with 96.43% sensitivity and 96.43% specificity in FFPE specimens. The diagnostic performance of the prediction model was reproducibly validated in BAL specimens for distinguishing SCC from AC with a higher accuracy compared with cytology (95.69 vs. 68.10%; P < 0.05). The prediction model might have a clinical value for accurately discriminating SCC from AC in both surgical lung tumor tissues and liquid cytological specimens.
引用
收藏
页码:50704 / 50714
页数:11
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