共 79 条
MicroRNAs and their target gene networks in breast cancer
被引:362
作者:

O'Day, Elizabeth
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机构: Harvard Univ, Childrens Hosp Boston, Program Cellular & Mol Med, Immune Dis Inst,Sch Med, Boston, MA 02115 USA

Lal, Ashish
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h-index: 0
机构:
Harvard Univ, Childrens Hosp Boston, Program Cellular & Mol Med, Immune Dis Inst,Sch Med, Boston, MA 02115 USA Harvard Univ, Childrens Hosp Boston, Program Cellular & Mol Med, Immune Dis Inst,Sch Med, Boston, MA 02115 USA
机构:
[1] Harvard Univ, Childrens Hosp Boston, Program Cellular & Mol Med, Immune Dis Inst,Sch Med, Boston, MA 02115 USA
来源:
BREAST CANCER RESEARCH
|
2010年
/
12卷
/
02期
关键词:
TRANSCRIPTIONAL REPRESSORS ZEB1;
CELL-PROLIFERATION;
E-CADHERIN;
TUMOR-SUPPRESSOR;
MIR-200;
FAMILY;
MESSENGER-RNA;
MESENCHYMAL TRANSITION;
CAENORHABDITIS-ELEGANS;
EPITHELIAL PHENOTYPE;
PROTEIN-SYNTHESIS;
D O I:
10.1186/bcr2484
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
MicroRNAs (miRNAs) are a major class of small endogenous RNA molecules that post-transcriptionally inhibit gene expression. Many miRNAs have been implicated in several human cancers, including breast cancer. Here we describe the association between altered miRNA signatures and breast cancer tumorigenesis and metastasis. The loss of several tumor suppressor miRNAs (miR-206, miR-17-5p, miR-125a, miR-125b, miR-200, let-7, miR-34 and miR-31) and the overexpression of certain oncogenic miRNAs (miR-21, miR-155, miR-10b, miR-373 and miR-520c) have been observed in many breast cancers. The gene networks orchestrated by these miRNAs are still largely unknown, although key targets have been identified that may contribute to the disease phenotype. Here we report how the observed perturbations in miRNA expression profiles may lead to disruption of key pathways involved in breast cancer.
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