Diagnostic and prognostic value of miR-106a in colorectal cancer

被引:20
作者
Hao, Haibin [1 ]
Liu, Laipeng [1 ]
Zhang, Dong [1 ]
Wang, Chao [1 ]
Xia, Guangfeng [1 ]
Zhong, Fuping [1 ]
Hu, Xiaoyun [1 ]
机构
[1] Nanchang Univ, Dept Gen Surg, Affiliated Hosp 2, Nanchang, Jiangxi, Peoples R China
关键词
miR106a; colorectal cancer; CRC; diagnosis; prognosis; PUBLICATION BIAS; EXPRESSION; MICRORNAS; METAANALYSIS; BIOMARKERS; RESISTANCE; QUALITY; MIRNAS; STAGE;
D O I
10.18632/oncotarget.13766
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We sought to systematically evaluate the diagnostic and prognostic value miR106a in patients with colorectal cancer (CRC). An original study was conducted to explore correlations between tissue miR106a levels and outcomes for 138 patients diagnosed with CRC. To explore the diagnostic performance of miR106a, eligible studies were identified from medical databases from China and abroad. Based on these results, 15 studies (including our original study) were pooled and included in a meta-analyses. The pooled sensitivity, specificity, and diagnostic odds ratios of miR106a were 0.53 (95% confidence interval (CI): 0.49-0.57), 0.85 (95% CI: 0.82-0.88), and 7.22 (95% CI: 3.17-16.44) for diagnosis of CRC, and the area under the curve (AUC) for miR106a when diagnosing CRC was 0.72. Patients with higher expression of tissue miR106a had poor overall survival (pooled hazard ratio (HR): 1.50; 95% CI: 1.02-2.20), but not disease-free survival (pooled HR: 1.03; 95% CI: 0.40-2.65). Overexpression of miR106a may predict superior metastasis-free survival (pooled HR: 0.65; 95% CI: 0.33-1.27), but the effect was not significant in this study (p = 0.21).
引用
收藏
页码:5038 / 5047
页数:10
相关论文
共 43 条
  • [1] MicroRNA expression patterns of tumors in early-onset colorectal cancer patients
    Ak, Secil
    Tunca, Berrin
    Tezcan, Gulcin
    Cecener, Gulsah
    Egeli, Unal
    Yilmazlar, Tuncay
    Ozturk, Ersin
    Yerci, Omer
    [J]. JOURNAL OF SURGICAL RESEARCH, 2014, 191 (01) : 113 - 122
  • [2] [Anonymous], 2001, METANINF: Stata Module to Evaluate Influence of a Single Study in Meta-analysis Estimation
  • [3] Circulating microRNAs: novel biomarkers for early detection of colorectal cancer
    Aravalli, Rajagopal N.
    Steer, Clifford J.
    [J]. TRANSLATIONAL RESEARCH, 2015, 166 (03) : 219 - 224
  • [4] Global patterns and trends in colorectal cancer incidence and mortality
    Arnold, Melina
    Sierra, Monica S.
    Laversanne, Mathieu
    Soerjomataram, Isabelle
    Jemal, Ahmedin
    Bray, Freddie
    [J]. GUT, 2017, 66 (04) : 683 - 691
  • [5] Likelihood ratio and Fagan's nomogram: 2 basic tools for the rational use of clinical laboratory tests
    Aznar-Oroval, E.
    Mancheno-Alvaro, A.
    Garcia-Lozano, T.
    Sanchez-Yepes, M.
    [J]. REVISTA DE CALIDAD ASISTENCIAL, 2013, 28 (06) : 390 - 391
  • [6] miRNA control of tumor cell invasion and metastasis
    Baranwal, Somesh
    Alahari, Suresh K.
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2010, 126 (06) : 1283 - 1290
  • [7] PUBLICATION BIAS - A PROBLEM IN INTERPRETING MEDICAL DATA
    BEGG, CB
    BERLIN, JA
    [J]. JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES A-STATISTICS IN SOCIETY, 1988, 151 : 419 - 463
  • [8] The Prognostic Value of MicroRNAs Varies with Patient Race/Ethnicity and Stage of Colorectal Cancer
    Bovell, Liselle C.
    Shanmugam, Chandrakumar
    Putcha, Balananda-Dhurjati K.
    Katkoori, Venkat R.
    Zhang, Bin
    Bae, Sejong
    Singh, Karan P.
    Grizzle, William E.
    Manne, Upender
    [J]. CLINICAL CANCER RESEARCH, 2013, 19 (14) : 3955 - 3965
  • [9] Brody H, 2015, NATURE, V526, pS1, DOI [10.1038/526S1a, 10.1038/521S1a]
  • [10] Frequent deletions and down-regulation of micro-RNA genes miR15 and miR16 at 13q14 in chronic lymphocytic leukemia
    Calin, GA
    Dumitru, CD
    Shimizu, M
    Bichi, R
    Zupo, S
    Noch, E
    Aldler, H
    Rattan, S
    Keating, M
    Rai, K
    Rassenti, L
    Kipps, T
    Negrini, M
    Bullrich, F
    Croce, CM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (24) : 15524 - 15529