High diagnostic value of miRNAs for NSCLC: quantitative analysis for both single and combined miRNAs in lung cancer

被引:16
作者
Yi, Minhan [1 ,2 ,3 ]
Liao, Zexi [1 ,4 ]
Deng, Langmei [1 ,5 ]
Xu, Li [1 ,2 ]
Tan, Yun [2 ]
Liu, Kun [2 ]
Chen, Ziliang [6 ]
Zhang, Yuan [1 ,3 ]
机构
[1] Cent South Univ, Xiangya Hosp, Dept Resp Med, Changsha, Hunan, Peoples R China
[2] Cent South Univ, Sch Life Sci, Changsha, Hunan, Peoples R China
[3] Cent South Univ, Xiangya Hosp, Natl Clin Res Ctr Geriatr Disorders, Changsha, Hunan, Peoples R China
[4] Cent South Univ, Xiangya Med Sch, Changsha, Hunan, Peoples R China
[5] Cent South Univ, Xiangya Hosp 3, Dept Emergency, Changsha, Hunan, Peoples R China
[6] Cent South Univ, Sch Comp Sci & Engn, Changsha, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
Lung cancer; microRNA; diagnostic biomarker; early diagnosis; NSCLC; MIR-30A EXPRESSION PROFILES; EXHALED BREATH CONDENSATE; BLOOD MONONUCLEAR-CELLS; PERIPHERAL-BLOOD; NONINVASIVE BIOMARKERS; BRONCHOALVEOLAR LAVAGE; CLINICAL-SIGNIFICANCE; POTENTIAL BIOMARKER; MICRORNA BIOMARKERS; TNM CLASSIFICATION;
D O I
10.1080/07853890.2021.2000634
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background MicroRNAs (miRNAs) are good candidates as biomarkers for Lung cancer (LC). The aim of this article is to figure out the diagnostic value of both single and combined miRNAs in LC. Methods Normative meta-analysis was conducted based on PRISMA. We assessed the diagnostic value by calculating the combined sensitivity (Sen), specificity (Spe), positive likelihood ratio (PLR), negative likelihood ratio (NLR) and diagnostic odds ratio (DOR) and the area under the curve (AUC) of single and combined miRNAs for LC and specific subgroups. Results A total of 80 qualified studies with a total of 8971 patients and 10758 controls were included. In non-small cell lung carcinoma (NSCLC), we involved 20 single-miRNAs and found their Sen, Spe and AUC ranged from 0.52-0.81, 0.66-0.88, and 0.68-0.90, respectively, specially, miR-19 with the maximum Sen, miR-20 and miR-10 with the highest Spe as well as miR-17 with the maximum AUC. Additionally, we detected miR-21 with the maximum Sen of 0.74 [95%CI: 0.62-0.83], miR-146 with the maximum Spe and AUC of 0.93 [95%CI: 0.79-0.98] and 0.89 [95%CI: 0.86-0.92] for early-stage NSCLC. We also identified the diagnostic power of available panel (miR-210, miR-31 and miR-21) for NSCLC with satisfying Sen, Spe and AUC of 0.82 [95%CI: 0.78-0.84], 0.87 [95%CI: 0.84-0.89] and 0.91 [95%CI: 0.88-0.93], and furtherly constructed 2 models for better diagnosis. Conclusions We identified several single miRNAs and combined groups with high diagnostic power for NSCLC through pooled quantitative analysis, which shows that specific miRNAs are good biomarker candidates for NSCLC and further researches needed.
引用
收藏
页码:2178 / 2193
页数:16
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