Combined Plasma MicroRNA and Fecal Occult Blood Tests in Early Detection of Colorectal Cancer

被引:8
作者
Luo, Xiaoya [1 ]
Wu, Yongdong [1 ]
Ji, Ming [1 ]
Zhang, Shutian [1 ]
机构
[1] Capital Med Univ, Beijing Friendship Hosp, Beijing Digest Dis Ctr,Beijing Key Lab Precancero, Dept Gastroenterol,Natl Clin Res Ctr Digest Dis, Beijing, Peoples R China
关键词
microRNA; plasma; fecal occult blood tests (FOBT); colorectal cancer; adenomas; early detection; CIRCULATING MICRORNAS; SERUM MIR-21; BIOMARKERS; DIAGNOSIS; EXPRESSION; PROGNOSIS; MARKERS;
D O I
10.7754/Clin.Lab.2018.180926
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Colorectal cancer (CRC) is one of the most common malignancies and a major cause of cancer-related death worldwide. Fecal occult blood tests (FOBT) are non-invasive colorectal cancer screening tests. In recent years plasma microRNAs (miRNAs) have shown great potential in early non-invasive cancer detection. Methods: FOBT (immunochemical) and a panel of 12 plasma miRNAs were tested in two independent groups: 57 CRC patients and 125 neoplasm free controls, in addition to 58 advanced adenoma patients and 67 neoplasm free controls. miRNA levels were assessed by quantitative real-time polymerase chain reaction (qRT-PCR). Results: Plasma levels of 7 miRNAs (miR-18a, miR-20a, miR-21, miR-92a, miR-133a, miR-143, miR-145) differed significantly between CRC patients and neoplasm free controls. miRNA plasma levels did not differ between advanced adenoma patients and controls. For 7 dysregulated miRNAs in CRC patients, AUCs ranged from 0.585 to 0.632 for CRC detection, in comparison to an AUC of 0.857 for iFOBT. The combination of miR-133a and iFOBT achieved a higher AUC (0.894) than iFOBT alone. At 97.8% specificity, miRNAs showed much lower sensitivities than iFOBT, but the miRNA panel and iFOBT in combination detected CRC with a higher sensitivity than iFOBT alone. Conclusions: The diagnostic performance of miRNAs was poorer than iFOBT. Nevertheless, plasma miRNA profiles offer an innovative non-invasive approach for early CRC detection. The potential advantage of combining plasma miRNA profiles with iFOBT needs to be further studied in a larger cohort of patients.
引用
收藏
页码:733 / 741
页数:9
相关论文
共 39 条
[1]   Bootstrap estimated true and false positive rates and ROC curve [J].
Adler, Werner ;
Lausen, Berthold .
COMPUTATIONAL STATISTICS & DATA ANALYSIS, 2009, 53 (03) :718-729
[2]   STATISTICAL PREDICTOR IDENTIFICATION [J].
AKAIKE, H .
ANNALS OF THE INSTITUTE OF STATISTICAL MATHEMATICS, 1970, 22 (02) :203-&
[3]  
[Anonymous], 2017, R Package Version 1
[4]  
[Anonymous], 2018, ANTI-CANCER DRUG, DOI [DOI 10.3322/caac.20115, DOI 10.1097/CAD.0000000000000617]
[5]   Global patterns and trends in colorectal cancer incidence and mortality [J].
Arnold, Melina ;
Sierra, Monica S. ;
Laversanne, Mathieu ;
Soerjomataram, Isabelle ;
Jemal, Ahmedin ;
Bray, Freddie .
GUT, 2017, 66 (04) :683-691
[6]   microRNA expression profile in stage III colorectal cancer: Circulating miR-18a and miR-29a as promising biomarkers [J].
Brunet Vega, Anna ;
Pericay, Carles ;
Moya, Irene ;
Ferrer, Anna ;
Dotor, Emma ;
Pisa, Aleydis ;
Casalots, Alex ;
Serra-Aracil, Xavier ;
Oliva, Joan-Carles ;
Ruiz, Anna ;
Saigi, Eugeni .
ONCOLOGY REPORTS, 2013, 30 (01) :320-326
[7]   Regulation of cancer metastasis by microRNAs [J].
Chan, Shih-Hsuan ;
Wang, Lu-Hai .
JOURNAL OF BIOMEDICAL SCIENCE, 2015, 22
[8]  
Chen WY, 2015, INT J CLIN EXP PATHO, V8, P7092
[9]   The use of circulating microRNAs as diagnostic biomarkers in colorectal cancer [J].
Clancy, Cillian ;
Joyce, Myles R. ;
Kerin, Michael J. .
CANCER BIOMARKERS, 2015, 15 (02) :103-113
[10]   MiR-17-92 cluster is associated with 13q gain and c-myc expression during colorectal adenoma to adenocarcinoma progression [J].
Diosdado, B. ;
van de Wiel, Ma ;
Droste, J. S. Terhaar Sive ;
Mongera, S. ;
Postma, C. ;
Meijerink, W. J. H. J. ;
Carvalho, B. ;
Meijer, G. A. .
BRITISH JOURNAL OF CANCER, 2009, 101 (04) :707-714