Serum miR-21 and miR-210 as promising non-invasive biomarkers for the diagnosis and prognosis of colorectal cancer

被引:17
作者
Li, Gang [1 ]
Wang, Qi [1 ]
Li, Zhenjun [1 ]
Shen, Yi [1 ]
机构
[1] Zhejiang Univ, Sch Med, Shaoxing Peoples Hosp, Dept Colorectal Surg,Shaoxing Hosp, 568 North Zhongxing Rd, Yuecheng Dist 312000, Shaoxing, Peoples R China
关键词
miR-21; miR-210; Serum; Colorectal cancer; Biomarkers; MICRORNAS; EXPRESSION; MARKER; RNA;
D O I
10.17235/reed.2020.6801/2019
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objective: this study aimed to investigate the expression and clinical significance of miR-21 and miR-210 in serum of patients with colorectal cancer (CRC). Methods: the expression levels of serum miR-21 and miR-210 in 40 CRC patients (CRC group) and 20 healthy patients (control group) were measured by qRT-PCR. Correlation analysis was performed of the relationship between serum miR-21 and miR-210 levels with clinical characteristics, including gender, age, tumor location, tumor size, tumor stage, local invasion and TNM staging. The expression levels of miR-21 and miR-210 in the CRC group were separately measured before and after surgery. ROC analysis was performed to evaluate the diagnostic value of miR-21 and miR-210. Results: serum miR-21 and miR-210 in the CRC group were much higher than those in the control group. Meanwhile, the levels of serum miR-21 and miR-210 were closely related to tumor size (p = 0.028, p = 0.047), lymphatic metastasis (p = 0.038, p = 0.028), TNM staging (p = 0.014, p = 0.047) and tumor stage (p = 0.014, p = 0.017), but independent of gender, age and tumor location. In addition, serum miR-21 and miR-210 in the CRC group (n = 18) after surgery were lower than those before surgery (p < 0.001). ROC curves showed that miR-21 (AUC = 0.863) and miR-210 (AUC 0.818) both had diagnostic efficacy in CRC patients. Conclusion: miR-21 and miR-210 can be used as novel noninvasive biomarkers for CRC diagnosis and prognosis.
引用
收藏
页码:832 / 837
页数:6
相关论文
共 37 条
[1]   Diversifying microRNA sequence and function [J].
Ameres, Stefan L. ;
Zamore, Phillip D. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2013, 14 (08) :475-488
[2]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[3]   Colorectal cancer [J].
Brenner, Hermann ;
Kloor, Matthias ;
Pox, Christian Peter .
LANCET, 2014, 383 (9927) :1490-1502
[4]   Relative and absolute risk of colorectal cancer for individuals with a family history: A meta-analysis [J].
Butterworth, AS ;
Higgins, JPT ;
Pharoah, P .
EUROPEAN JOURNAL OF CANCER, 2006, 42 (02) :216-227
[5]   Secreted microRNAs: a new form of intercellular communication [J].
Chen, Xi ;
Liang, Hongwei ;
Zhang, Junfeng ;
Zen, Ke ;
Zhang, Chen-Yu .
TRENDS IN CELL BIOLOGY, 2012, 22 (03) :125-132
[6]   Detection and characterization of placental MicroRNAs in maternal plasma [J].
Chim, Stephen S. C. ;
Shing, Tristan K. F. ;
Hung, Emily C. W. ;
Leung, Tak-yeung ;
Lau, Tze-kin ;
Chiu, Rossa W. K. ;
Lo, Y. M. Dennis .
CLINICAL CHEMISTRY, 2008, 54 (03) :482-490
[7]   MicroRNAs in body fluids-the mix of hormones and biomarkers [J].
Cortez, Maria Angelica ;
Bueso-Ramos, Carlos ;
Ferdin, Jana ;
Lopez-Berestein, Gabriel ;
Sood, Anil K. ;
Calin, George A. .
NATURE REVIEWS CLINICAL ONCOLOGY, 2011, 8 (08) :467-477
[8]   Predictive and prognostic biomarkers in colorectal cancer: A systematic review of recent advances and challenges [J].
Das, Vishal ;
Kalita, Jatin ;
Pal, Mintu .
BIOMEDICINE & PHARMACOTHERAPY, 2017, 87 :8-19
[9]   Impact of Cellular miRNAs on Circulating miRNA Biomarker Signatures [J].
Duttagupta, Radha ;
Jiang, Rong ;
Gollub, Jeremy ;
Getts, Robert C. ;
Jones, Keith W. .
PLOS ONE, 2011, 6 (06)
[10]  
Fakih MG, 2006, ONCOLOGY-NY, V20, P579