Plasma microRNAs are promising novel biomarkers for early detection of colorectal cancer

被引:770
作者
Huang, Zhaohui [1 ,2 ,3 ,4 ]
Huang, Dan [1 ,2 ,3 ]
Ni, Shujuan [1 ,2 ,3 ]
Peng, Zhilei [1 ,2 ,3 ]
Sheng, Weiqi [1 ,2 ,3 ]
Du, Xiang [1 ,2 ,3 ]
机构
[1] Fudan Univ, Canc Hosp, Dept Pathol, Shanghai 200433, Peoples R China
[2] Fudan Univ, Shanghai Med Sch, Dept Oncol, Shanghai 200433, Peoples R China
[3] Fudan Univ, Inst Biomed Sci, Shanghai 200433, Peoples R China
[4] Suzhou Univ, Affiliated Hosp 4, Wuxi Oncol Inst, Wuxi, Peoples R China
关键词
MicroRNA; colorectal carcinoma; plasma; early diagnosis; REAL-TIME PCR; EXPRESSION PROFILES; MIR-17-92; CLUSTER; LUNG-CANCER; SERUM; COLON; IDENTIFICATION; POLYCISTRON;
D O I
10.1002/ijc.25007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNA (miRNA) opens up a new field for molecular diagnosis of cancer. However, the role of circulating miRNAs in plasma/ serum in cancer diagnosis is not clear. The aim of this study was to investigate whether plasma miRNAs can be used as biomarkers for the early detection of colorectal carcinoma (CRC). We measured the levels of 12 miRNAs (miR-134, 146a, -17-3p, -181d, -191, -221, -222, -223, -25, -29a, -320a and -92a) in plasma samples from patients with advanced colorectal neoplasia (carcinomas and advanced adenomas) and healthy controls using real-time RT-PCR. We found that plasma miR-29a and miR-92a have significant diagnostic value for advanced neoplasia. MiR-29a yielded an AUC (the areas under the ROC curve) of 0.844 and miR-92a yielded an AUC of 0.838 in discriminating CRC from controls. More importantly, these 2 miRNAs also could discriminate advanced adenomas from controls and yielded an AUC of 0.769 for miR-29a and 0.749 for miR-92a. Combined ROC analyses using these 2 miRNAs revealed an elevated AUC of 0.883 with 83.0% sensitivity and 84.7% specificity in discriminating CRC, and AUC of 0.773 with 73.0% sensitivity and 79.7% specificity in discriminating advanced adenomas. Collectively, these data suggest that plasma miR-29a and miR-92a have strong potential as novel noninvasive biomarkers for early detection of CRC.
引用
收藏
页码:118 / 126
页数:9
相关论文
共 35 条
  • [1] MicroRNA regulation of a cancer network: Consequences of the feedback loops involving miR-17-92, E2F, and Myc
    Aguda, Baltazar D.
    Kim, Yangjin
    Piper-Hunter, Melissa G.
    Friedman, Avner
    Marsh, Clay B.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (50) : 19678 - 19683
  • [2] Identification by Real-time PCR of 13 mature microRNAs differentially expressed in colorectal cancer and non-tumoral tissues
    Bandres, E.
    Cubedo, E.
    Agirre, X.
    Malumbres, R.
    Zarate, R.
    Ramirez, N.
    Abajo, A.
    Navarro, A.
    Moreno, I.
    Monzo, M.
    Garcia-Foncillas, J.
    [J]. MOLECULAR CANCER, 2006, 5 (1)
  • [3] MicroRNA deregulation and pathway alterations in nasopharyngeal carcinoma
    Chen, H-C
    Chen, G-H
    Chen, Y-H
    Liao, W-L
    Liu, C-Y
    Chang, K-P
    Chang, Y-S
    Chen, S-J
    [J]. BRITISH JOURNAL OF CANCER, 2009, 100 (06) : 1002 - 1011
  • [4] Characterization of microRNAs in serum: a novel class of biomarkers for diagnosis of cancer and other diseases
    Chen, Xi
    Ba, Yi
    Ma, Lijia
    Cai, Xing
    Yin, Yuan
    Wang, Kehui
    Guo, Jigang
    Zhang, Yujing
    Chen, Jiangning
    Guo, Xing
    Li, Qibin
    Li, Xiaoying
    Wang, Wenjing
    Zhang, Yan
    Wang, Jin
    Jiang, Xueyuan
    Xiang, Yang
    Xu, Chen
    Zheng, Pingping
    Zhang, Juanbin
    Li, Ruiqiang
    Zhang, Hongjie
    Shang, Xiaobin
    Gong, Ting
    Ning, Guang
    Wang, Jun
    Zen, Ke
    Zhang, Junfeng
    Zhang, Chen-Yu
    [J]. CELL RESEARCH, 2008, 18 (10) : 997 - 1006
  • [5] Detection and characterization of placental MicroRNAs in maternal plasma
    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
    [J]. CLINICAL CHEMISTRY, 2008, 54 (03) : 482 - 490
  • [6] Elevated expression of the miR-17-92 polycistron and miR-21 in hepadnavirus-associated hepatocellular carcinoma contributes to the malignant phenotype
    Connolly, Erin
    Melegari, Margherita
    Landgraf, Pablo
    Tchaikovskaya, Tatyana
    Tennant, Bud C.
    Slagle, Betty L.
    Rogler, Leslie E.
    Zavolan, Mihaela
    Tuschl, Thomas
    Rogler, Charles E.
    [J]. AMERICAN JOURNAL OF PATHOLOGY, 2008, 173 (03) : 856 - 864
  • [7] MicroRNA-29 family reverts aberrant methylation in lung cancer by targeting DNA methyltransferases 3A and 3B
    Fabbri, Muller
    Garzon, Ramiro
    Cimmino, Amelia
    Liu, Zhongfa
    Zanesi, Nicola
    Callegari, Elisa
    Liu, Shujun
    Alder, Hansjuerg
    Costinean, Stefan
    Fernandez-Cymering, Cecilia
    Volinia, Stefano
    Guler, Gulnur
    Morrison, Carl D.
    Chan, Kenneth K.
    Marcucci, Guido
    Calin, George A.
    Huebner, Kay
    Croce, Carlo M.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (40) : 15805 - 15810
  • [8] miR-29a suppresses tristetraprolin, which is a regulator of epithelial polarity and metastasis
    Gebeshuber, Christoph A.
    Zatloukal, Kurt
    Martinez, Javier
    [J]. EMBO REPORTS, 2009, 10 (04) : 400 - 405
  • [9] A polycistronic microRNA cluster, miR-17-92, is overexpressed in human lung cancers and enhances cell proliferation
    Hayashita, Y
    Osada, H
    Tatematsu, Y
    Yamada, H
    Yanagisawa, K
    Tomida, S
    Yatabe, Y
    Kawahara, K
    Sekido, Y
    Takahashi, T
    [J]. CANCER RESEARCH, 2005, 65 (21) : 9628 - 9632
  • [10] A microRNA polycistron as a potential human oncogene
    He, L
    Thomson, JM
    Hemann, MT
    Hernando-Monge, E
    Mu, D
    Goodson, S
    Powers, S
    Cordon-Cardo, C
    Lowe, SW
    Hannon, GJ
    Hammond, SM
    [J]. NATURE, 2005, 435 (7043) : 828 - 833