MicroRNAs as novel biological targets for detection and regulation

被引:239
作者
Li, Jinbo [1 ]
Tan, Subee [2 ]
Kooger, Romain [1 ]
Zhang, Chenyu [2 ]
Zhang, Yan [1 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Analyt Chem Life Sci, Nanjing 210093, Jiangsu, Peoples R China
[2] Nanjing Univ, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, Nanjing 210093, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
NUCLEIC-ACID; RNA INTERFERENCE; CANCER; DELIVERY; EXPRESSION; PROBE; AMPLIFICATION; INHIBITION;
D O I
10.1039/c3cs60312a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
MicroRNAs are being considered as a novel type of bio-markers and potential therapeutic targets for various diseases. Diverse chemical tools are being developed for the detection or regulation of microRNAs with bio-medical implications. Chemical probes have been developed for use in combination with in situ signal amplification strategies to realize sensitive detection of microRNAs of low abundance. Regulation of microRNAs aberrantly expressed in tumours represents a new approach to cancer chemotherapy. Synthetic oligonucleotides including antisense oligonucleotides and microRNA mimics have been successfully delivered into cells or tissues to inhibit or enhance the function of specific endogenous microRNAs. Small-molecule modifiers of microRNAs that modify the expression or function of endogenous microRNAs are emerging not only as useful probes to explore microRNA-involved regulatory networks, but also as potential therapeutic reagents. In this tutorial review, we discuss the strategies developed by chemists in recent years for microRNA detection and regulation, with a focus on the potential of these chemical tools in microRNA-related biomedical applications.
引用
收藏
页码:506 / 517
页数:12
相关论文
共 50 条
[1]  
Bader Andreas G., 2012, Frontiers in Genetics, V3, P120, DOI 10.3389/fgene.2012.00120
[2]   The Promise of MicroRNA Replacement Therapy [J].
Bader, Andreas G. ;
Brown, David ;
Winkler, Matthew .
CANCER RESEARCH, 2010, 70 (18) :7027-7030
[3]   In vitro quantification of specific microRNA using molecular beacons [J].
Baker, Meredith B. ;
Bao, Gang ;
Searles, Charles D. .
NUCLEIC ACIDS RESEARCH, 2012, 40 (02) :e13
[4]   MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[5]   The Tuberculosis Drug Streptomycin as a Potential Cancer Therapeutic: Inhibition of miR-21 Function by Directly Targeting Its Precursor [J].
Bose, Debojit ;
Jayaraj, Gopal ;
Suryawanshi, Hemant ;
Agarwala, Prachi ;
Pore, Subrata Kumar ;
Banerjee, Rajkumar ;
Maiti, Souvik .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2012, 51 (04) :1019-1023
[6]   First microRNA mimic enters clinic [J].
Bouchie, Aaron .
NATURE BIOTECHNOLOGY, 2013, 31 (07) :577-577
[7]   Characterization of microRNAs in serum: a novel class of biomarkers for diagnosis of cancer and other diseases [J].
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 .
CELL RESEARCH, 2008, 18 (10) :997-1006
[8]   A universal activator of microRNAs identified from photoreaction products [J].
Chen, Xuejiao ;
Huang, Chengmei ;
Zhang, Wenjie ;
Wu, Yihan ;
Chen, Xi ;
Zhang, Chen-Yu ;
Zhang, Yan .
CHEMICAL COMMUNICATIONS, 2012, 48 (51) :6432-6434
[9]   Highly Sensitive Determination of microRNA Using Target-Primed and Branched Rolling-Circle Amplification [J].
Cheng, Yongqiang ;
Zhang, Xian ;
Li, Zhengping ;
Jiao, Xiaoxia ;
Wang, Yucong ;
Zhang, Yali .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2009, 48 (18) :3268-3272
[10]   Single-stranded microRNA mimics [J].
Chorn, Guillaume ;
Klein-McDowell, Molly ;
Zhao, Lihong ;
Saunders, Matthew A. ;
Flanagan, W. Michael ;
Willingham, Aarron T. ;
Lim, Lee P. .
RNA, 2012, 18 (10) :1796-1804