microRNAs as oncogenes and tumor suppressors

被引:2192
作者
Zhang, Baohong [1 ]
Pan, Xiaoping [1 ]
Cobb, George P. [1 ]
Anderson, Todd A. [1 ]
机构
[1] Texas Tech Univ, Dept Environm Toxicol, Inst Environm & Human Hlth, Lubbock, TX 79409 USA
关键词
microRNA; cancer; oncogene; tumor suppressor; apoptosis; gene regulation; gene therapy;
D O I
10.1016/j.ydbio.2006.08.028
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
microRNAs (miRNAs) are a new class of non-protein-coding, endogenous, small RNAs. They are important regulatory molecules in animals and plants. miRNA regulates gene expression by translational repression, mRNA cleavage, and mRNA decay initiated by miRNA-guided rapid deadenylation. Recent Studies show that some miRNAs regulate cell proliferation and apoptosis processes that are important in cancer formation. By using multiple molecular techniques, which include Northern blot analysis, real-time PCR, miRNA microarray, up- or down-expression of specific miRNAs, it was found that several miRNAs were directly involved in human cancers, including lung, breast, brain, liver, colon cancer, and leukemia. In addition, some miRNAs may function as oncogenes or tumor suppressors. More than 50% of miRNA genes are located in cancer-associated genomic regions or in fragile sites, Suggesting that miRNAs may play a more important role in the pathogenesis of a limited range of human cancers than previously thought. Overexpressed miRNAs in cancers, such as mir-17-92, may function as oncogenes and promote cancer development by negatively regulating tumor suppressor genes and/or genes that control cell differentiation or apoptosis. Underexpressed miRNAs in cancers, such as let-7, function as tumor suppressor genes and may inhibit cancers by regulating oncogenes and/or genes that control cell differentiation or apoptosis. miRNA expression profiles may become useful biomarkers for cancer diagnostics. In addition, miRNA therapy could be a powerful tool for cancer prevention and therapeutics. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 12
页数:12
相关论文
共 124 条
[61]   Computational identification of Drosophila microRNA genes -: art. no. R42 [J].
Lai, EC ;
Tomancak, P ;
Williams, RW ;
Rubin, GM .
GENOME BIOLOGY, 2003, 4 (07)
[62]   Micro RNAs are complementary to 3′ UTR sequence motifs that mediate negative post-transcriptional regulation [J].
Lai, EC .
NATURE GENETICS, 2002, 30 (04) :363-364
[63]   The human DiGeorge syndrome critical region gene 8 and its D-melanogaster homolog are required for miRNA biogenesis [J].
Landthaler, M ;
Yalcin, A ;
Tuschl, T .
CURRENT BIOLOGY, 2004, 14 (23) :2162-2167
[64]   An abundant class of tiny RNAs with probable regulatory roles in Caenorhabditis elegans [J].
Lau, NC ;
Lim, LP ;
Weinstein, EG ;
Bartel, DP .
SCIENCE, 2001, 294 (5543) :858-862
[65]   An extensive class of small RNAs in Caenorhabditis elegans [J].
Lee, RC ;
Ambros, V .
SCIENCE, 2001, 294 (5543) :862-864
[66]   THE C-ELEGANS HETEROCHRONIC GENE LIN-4 ENCODES SMALL RNAS WITH ANTISENSE COMPLEMENTARITY TO LIN-14 [J].
LEE, RC ;
FEINBAUM, RL ;
AMBROS, V .
CELL, 1993, 75 (05) :843-854
[67]   MicroRNA genes are transcribed by RNA polymerase II [J].
Lee, Y ;
Kim, M ;
Han, JJ ;
Yeom, KH ;
Lee, S ;
Baek, SH ;
Kim, VN .
EMBO JOURNAL, 2004, 23 (20) :4051-4060
[68]   MicroRNA maturation: stepwise processing and subcellular localization [J].
Lee, Y ;
Jeon, K ;
Lee, JT ;
Kim, S ;
Kim, VN .
EMBO JOURNAL, 2002, 21 (17) :4663-4670
[69]   Disentangling the MYC web [J].
Levens, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (09) :5757-5759
[70]   Prediction of mammalian microRNA targets [J].
Lewis, BP ;
Shih, IH ;
Jones-Rhoades, MW ;
Bartel, DP ;
Burge, CB .
CELL, 2003, 115 (07) :787-798