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

被引:929
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
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