Source:http://linkedlifedata.com/resource/pubmed/id/17072344
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
19
|
pubmed:dateCreated |
2007-4-26
|
pubmed:abstractText |
MicroRNAs (miRNAs) are approximately 22 nucleotide non-coding RNA molecules that regulate gene expression post-transcriptionally. Although aberrant expression of miRNAs in various human cancers suggests a role for miRNAs in tumorigenesis, it remains largely unclear as to whether knockdown of a specific miRNA affects tumor growth. In this study, we profiled miRNA expression in matched normal breast tissue and breast tumor tissues by TaqMan real-time polymerase chain reaction miRNA array methods. Consistent with previous findings, we found that miR-21 was highly overexpressed in breast tumors compared to the matched normal breast tissues among 157 human miRNAs analysed. To better evaluate the role of miR-21 in tumorigenesis, we transfected breast cancer MCF-7 cells with anti-miR-21 oligonucleotides and found that anti-miR-21 suppressed both cell growth in vitro and tumor growth in the xenograft mouse model. Furthermore, this anti-miR-21-mediated cell growth inhibition was associated with increased apoptosis and decreased cell proliferation, which could be in part owing to downregulation of the antiapoptotic Bcl-2 in anti-miR-21-treated tumor cells. Together, these results suggest that miR-21 functions as an oncogene and modulates tumorigenesis through regulation of genes such as bcl-2 and thus, it may serve as a novel therapeutic target.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Apr
|
pubmed:issn |
0950-9232
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
26
|
pubmed:volume |
26
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
2799-803
|
pubmed:dateRevised |
2007-12-3
|
pubmed:meshHeading |
pubmed-meshheading:17072344-Animals,
pubmed-meshheading:17072344-Apoptosis,
pubmed-meshheading:17072344-Breast,
pubmed-meshheading:17072344-Breast Neoplasms,
pubmed-meshheading:17072344-Cell Proliferation,
pubmed-meshheading:17072344-Female,
pubmed-meshheading:17072344-Gene Expression Regulation, Neoplastic,
pubmed-meshheading:17072344-Humans,
pubmed-meshheading:17072344-Mice,
pubmed-meshheading:17072344-Mice, Nude,
pubmed-meshheading:17072344-MicroRNAs,
pubmed-meshheading:17072344-Oligonucleotides, Antisense,
pubmed-meshheading:17072344-Proto-Oncogene Proteins c-bcl-2,
pubmed-meshheading:17072344-RNA, Messenger,
pubmed-meshheading:17072344-RNA Processing, Post-Transcriptional,
pubmed-meshheading:17072344-Xenograft Model Antitumor Assays
|
pubmed:year |
2007
|
pubmed:articleTitle |
miR-21-mediated tumor growth.
|
pubmed:affiliation |
Department of Medical Microbiology, Immunology and Cell Biology, Southern Illinois University School of Medicine, Springfield, IL 62794, USA.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, N.I.H., Extramural
|