共 33 条
Circular RNA and miR-7 in Cancer
被引:981
作者:

Hansen, Thomas B.
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h-index: 0
机构:
Aarhus Univ, Dept Mol Biol & Genet, DK-8000 Aarhus C, Denmark Aarhus Univ, Dept Mol Biol & Genet, DK-8000 Aarhus C, Denmark

Kjems, Jorgen
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h-index: 0
机构:
Aarhus Univ, Dept Mol Biol & Genet, DK-8000 Aarhus C, Denmark
Aarhus Univ, Interdisciplinary Nanosci Ctr iNANO, DK-8000 Aarhus C, Denmark Aarhus Univ, Dept Mol Biol & Genet, DK-8000 Aarhus C, Denmark

Damgaard, Christian K.
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机构:
Aarhus Univ, Dept Mol Biol & Genet, DK-8000 Aarhus C, Denmark Aarhus Univ, Dept Mol Biol & Genet, DK-8000 Aarhus C, Denmark
机构:
[1] Aarhus Univ, Dept Mol Biol & Genet, DK-8000 Aarhus C, Denmark
[2] Aarhus Univ, Interdisciplinary Nanosci Ctr iNANO, DK-8000 Aarhus C, Denmark
关键词:
NEOPLASTIC CEREBELLAR DEGENERATION;
GROWTH-FACTOR RECEPTOR;
STEM-CELLS;
MICRORNA-7;
EXPRESSION;
PROTEIN;
PATHWAY;
GLIOBLASTOMA;
ROBUSTNESS;
TURNOVER;
D O I:
10.1158/0008-5472.CAN-13-1568
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
MicroRNAs (miRNA) play important roles in fine-tuning gene expression and are often deregulated in cancer. The identification of competing endogenous RNA and circular RNA (circRNA) as important regulators of miRNA activity underscores the increasing complexity of ncRNA-mediated regulatory networks. Particularly, the recently identified circular RNA, ciRS-7, which acts as a designated miR-7 inhibitor/sponge, has conceptually changed the mechanistic understanding of miRNA networks. As miR-7 modulates the expression of several oncogenes, disclosing the regulation of miR-7 activity will likely advance the understanding of various cancer etiologies. Here, we review the current knowledge about the ciRS-7/miR-7 axis in cancer-related pathways and discuss possible models explaining the relevance of coexpressing miR-7 along with a circRNA inhibitor. (C)2013 AACR.
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页码:5609 / 5612
页数:4
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