Serum levels of candidate microRNA diagnostic markers differ among the stages of non-small-cell lung cancer

被引:49
作者
Aiso, Toshiko [1 ]
Ohtsuka, Kouki [2 ]
Ueda, Makiko [1 ]
Karita, Shin [3 ,4 ]
Yokoyama, Takuma [5 ]
Takata, Saori
Matsuki, Naoko [6 ]
Kondo, Haruhiko [3 ]
Takizawa, Hajime [5 ]
Okada, Annabelle A. [6 ]
Watanabe, Takashi [2 ]
Ohnishi, Hiroaki [2 ]
机构
[1] Kyorin Univ, Fac Hlth Sci, Dept Med Technol, 5-4-1 Shimorenjaku, Mitaka, Tokyo 1818612, Japan
[2] Kyorin Univ, Dept Lab Med, Sch Med, Tokyo 1818611, Japan
[3] Kyorin Univ, Dept Gen Thorac Surg, Sch Med, Tokyo 1818611, Japan
[4] JR Tokyo Gen Hosp, Dept Thorac Surg, Tokyo 1518528, Japan
[5] Kyorin Univ, Sch Med, Dept Resp Med, Tokyo 1818611, Japan
[6] Kyorin Univ, Sch Med, Dept Ophthalmol, Tokyo 1818611, Japan
关键词
circulating microRNAs; biomarkers; resection; TaqMan; reverse transcription-quantitative polymerase chain reaction; NONINVASIVE BIOMARKERS; CIRCULATING MICRORNAS; POTENTIAL BIOMARKER; PLASMA; IDENTIFICATION; MIR-21; MIRNAS; PANEL; MIR-145; PCR;
D O I
10.3892/ol.2018.9464
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Circulating microRNAs (miRNAs) are promising markers for cancer diagnosis and prognosis. Numerous studies evaluating miRNAs as markers for non-small cell lung cancer (NSCLC) have been conducted in recent years; however, the majority of candidate markers proposed via individual studies were inconsistent and no marker miRNAs for the diagnosis of early stage NSCLC have been established. In the present study, miR-145, miR-20a, miR-21 and miR-223, which were previously reported as candidate diagnostic markers of NSCLC, were re-evaluated. The serum levels of these miRNAs were quantified in 56 patients with stage I-IV NSCLC using the TaqMan microRNA assays and separately compared the levels at each stage with those in 26 control patients. The level of miR-145 was significantly reduced in patients with NSCLC, regardless of clinical stage, and its level increased following tumor resection in patients with stage I-II disease. These results indicate that miR-145 is relevant as a diagnostic marker for stages I-IV NSCLC. Additionally, the levels of miR-20a and miR-21 demonstrated notable differences among patients at different clinical stages. These miRNAs distinguished patients in a number of, but not all, stages of NSCLC from cancer-free control patients. These results indicated that it is essential to analyze miRNA levels at each stage separately in order to evaluate marker miRNAs for NSCLC diagnosis.
引用
收藏
页码:6643 / 6651
页数:9
相关论文
共 48 条
[1]
[Anonymous], CANC GENET
[2]
[Anonymous], AM J CLIN PATHOL
[3]
Armand-Labit Virginie, 2017, BioMolecular Concepts, V8, P61, DOI 10.1515/bmc-2017-0002
[4]
Argonaute2 complexes carry a population of circulating microRNAs independent of vesicles in human plasma [J].
Arroyo, Jason D. ;
Chevillet, John R. ;
Kroh, Evan M. ;
Ruf, Ingrid K. ;
Pritchard, Colin C. ;
Gibson, Donald F. ;
Mitchell, Patrick S. ;
Bennett, Christopher F. ;
Pogosova-Agadjanyan, Era L. ;
Stirewalt, Derek L. ;
Tait, Jonathan F. ;
Tewari, Muneesh .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (12) :5003-5008
[5]
Comparisons of microRNA Patterns in Plasma before and after Tumor Removal Reveal New Biomarkers of Lung Squamous Cell Carcinoma [J].
Aushev, Vasily N. ;
Zborovskaya, Irina B. ;
Laktionov, Konstantin K. ;
Girard, Nicolas ;
Cros, Marie-Pierre ;
Herceg, Zdenko ;
Krutovskikh, Vladimir .
PLOS ONE, 2013, 8 (10)
[6]
A serum circulating miRNA diagnostic test to identify asymptomatic high-risk individuals with early stage lung cancer [J].
Bianchi, Fabrizio ;
Nicassio, Francesco ;
Marzi, Matteo ;
Belloni, Elena ;
Dall'Olio, Valentina ;
Bernard, Loris ;
Pelosi, Giuseppe ;
Maisonneuve, Patrick ;
Veronesi, Giulia ;
Di Fiore, Pier Paolo .
EMBO MOLECULAR MEDICINE, 2011, 3 (08) :495-503
[7]
Identification of ten serum microRNAs from a genome-wide serum microRNA expression profile as novel noninvasive biomarkers for nonsmall cell lung cancer diagnosis [J].
Chen, Xi ;
Hu, Zhibin ;
Wang, Wenjing ;
Ba, Yi ;
Ma, Lijia ;
Zhang, Chunni ;
Wang, Cheng ;
Ren, Zhiji ;
Zhao, Yang ;
Wu, Sijia ;
Zhuang, Rui ;
Zhang, Yixin ;
Hu, Heng ;
Liu, Chazhen ;
Xu, Lin ;
Wang, Jun ;
Shen, Hongbing ;
Zhang, Junfeng ;
Zen, Ke ;
Zhang, Chen-Yu .
INTERNATIONAL JOURNAL OF CANCER, 2012, 130 (07) :1620-1628
[8]
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
[9]
A Differentiation-Based MicroRNA Signature Identifies Leiomyosarcoma as a Mesenchymal Stem Cell-Related Malignancy [J].
Danielson, Laura S. ;
Menendez, Silvia ;
Attolini, Camille Stephan-Otto ;
Guijarro, Maria V. ;
Bisogna, Maria ;
Wei, Jianjun ;
Socci, Nicholas D. ;
Levine, Douglas A. ;
Michor, Franziska ;
Hernando, Eva .
AMERICAN JOURNAL OF PATHOLOGY, 2010, 177 (02) :908-917
[10]
Implications of miR cluster 143/145 as universal anti-oncomiRs and their dysregulation during tumorigenesis [J].
Das, Ani V. ;
Pillai, Radhakrishna M. .
CANCER CELL INTERNATIONAL, 2015, 15