Programmed cell death 4 (PDCD4) is an important functional target of the microRNA miR-21 in breast cancer cells

被引:937
作者
Frankel, Lisa B. [1 ]
Christoffersen, Nanna R. [1 ]
Jacobsen, Anders [1 ,2 ]
Lindow, Morten [1 ,2 ]
Krogh, Anders [1 ,2 ]
Lund, Anders H. [1 ,3 ]
机构
[1] Univ Copenhagen, Biotech Res & Innovat Ctr, DK-2200 Copenhagen, Denmark
[2] Univ Copenhagen, Bioinformat Ctr, DK-2200 Copenhagen, Denmark
[3] Univ Copenhagen, Ctr Epigenet, DK-2200 Copenhagen, Denmark
关键词
D O I
10.1074/jbc.M707224200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs are emerging as important regulators of cancer-related processes. The miR-21 microRNA is overexpressed in a wide variety of cancers and has been causally linked to cellular proliferation, apoptosis, and migration. Inhibition of mir-21 in MCF-7 breast cancer cells causes reduced cell growth. Using array expression analysis of MCF-7 cells depleted of miR-21, we have identified mRNA targets of mir-21 and have shown a link between miR-21 and the p53 tumor suppressor protein. We furthermore found that the tumor suppressor protein Programmed Cell Death 4 (PDCD4) is regulated by miR-21 and demonstrated that PDCD4 is a functionally important target for miR-21 in breast cancer cells.
引用
收藏
页码:1026 / 1033
页数:8
相关论文
共 61 条
[31]   The diverse functions of MicroRNAs in animal development and disease [J].
Kloosterman, Wigard P. ;
Plasterk, Ronald H. A. .
DEVELOPMENTAL CELL, 2006, 11 (04) :441-450
[32]   Silencing of microRNAs in vivo with 'antagomirs' [J].
Krützfeldt, J ;
Rajewsky, N ;
Braich, R ;
Rajeev, KG ;
Tuschl, T ;
Manoharan, M ;
Stoffel, M .
NATURE, 2005, 438 (7068) :685-689
[33]   Identification of novel genes coding for small expressed RNAs [J].
Lagos-Quintana, M ;
Rauhut, R ;
Lendeckel, W ;
Tuschl, T .
SCIENCE, 2001, 294 (5543) :853-858
[34]   Programmed cell death protein 4 (pdcd4):: A novel target for antineoplastic therapy? [J].
Lankat-Buttgereit, B ;
Göke, R .
BIOLOGY OF THE CELL, 2003, 95 (08) :515-519
[35]   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
[36]   An extensive class of small RNAs in Caenorhabditis elegans [J].
Lee, RC ;
Ambros, V .
SCIENCE, 2001, 294 (5543) :862-864
[37]   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
[38]   Coordination and communication between the p53 and IGF-1-AKT-TOR signal transduction pathways [J].
Levine, AJ ;
Feng, ZH ;
Mak, TW ;
You, H ;
Jin, SK .
GENES & DEVELOPMENT, 2006, 20 (03) :267-275
[39]   Microarray analysis shows that some microRNAs downregulate large numbers of target mRNAs [J].
Lim, LP ;
Lau, NC ;
Garrett-Engele, P ;
Grimson, A ;
Schelter, JM ;
Castle, J ;
Bartel, DP ;
Linsley, PS ;
Johnson, JM .
NATURE, 2005, 433 (7027) :769-773
[40]   MicroRNA expression profiles classify human cancers [J].
Lu, J ;
Getz, G ;
Miska, EA ;
Alvarez-Saavedra, E ;
Lamb, J ;
Peck, D ;
Sweet-Cordero, A ;
Ebet, BL ;
Mak, RH ;
Ferrando, AA ;
Downing, JR ;
Jacks, T ;
Horvitz, HR ;
Golub, TR .
NATURE, 2005, 435 (7043) :834-838