Tumor-Derived Exosomal miR-620 as a Diagnostic Biomarker in Non-Small-Cell Lung Cancer

被引:27
|
作者
Tang, Youyong [1 ]
Zhang, Zhijun [2 ]
Song, Xingguo [3 ]
Yu, Miao [4 ]
Niu, Limin [1 ]
Zhao, Yajing [1 ]
Wang, Li [1 ]
Song, Xianrang [1 ]
Xie, Li [1 ]
机构
[1] Shandong First Med Univ & Shandong Acad Med Sci, Shandong Canc Hosp & Inst, Dept Clin Lab, Jinan, Peoples R China
[2] Taian City Cent Hosp, Dept Clin Lab, Tai An, Peoples R China
[3] Shandong First Med Univ & Shandong Acad Med Sci, Shandong Canc Hosp & Inst, Shandong Prov Key Lab Radiat Oncol, Jinan, Peoples R China
[4] Shandong Univ, Shandong Prov Hosp 3, Cheeloo Coll Med, Dept Clin Lab, Jinan, Peoples R China
基金
中国国家自然科学基金;
关键词
CIRCULATING BIOMARKERS; MICRORNAS; RNA; STAGE;
D O I
10.1155/2020/6691211
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. Evidence has suggested the functional role of exosomal miRNAs in cancer diagnosis. This study aimed to determine whether the serum exosomal biomarkers can improve the diagnosis of patients with non-small-cell lung cancer (NSCLC). Materials and Methods. The exosomes were extracted from the serum of NSCLC patients (n = 235) and healthy donors (n = 231) using ultracentrifugation and then were evaluated by using transmission electron microscopy, qNano, and western blotting. The serum exosomal miRNA expression was validated using qPCR. Results. Exosomal miR-620 was significantly reduced in NSCLC and early-stage NSCLC patients (P<0.0001) when compared to that of healthy controls, with an area under the curve (AUC) of 0.728 and 0.707, respectively. Exosomal miR-620 expression showed an association with drinking (P=0.008) and distant metastasis (P=0.037). Additionally, the downregulated exosomal miR-620 showed association with chemotherapeutic effect (P=0.044). Conclusion. These findings suggest the serum exosomal miR-620 as a promising diagnostic and prognostic noninvasive biomarker in NSCLC patients.
引用
收藏
页数:9
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