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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
12
pubmed:dateCreated
2011-2-25
pubmed:abstractText
MicroRNAs (miRNAs) are small noncoding RNAs that post-transcriptionally regulate gene expression. There have been several reports of miRNA deregulation in prostate cancer (PCa) and the biological evidence for an involvement of miRNAs in prostate tumorigenesis is increasing. In this study, we show that miR-34c is downregulated in PCa (p = 0.0005) by performing qRT-PCR on 49 TURPs from PCa patients compared to 25 from patients with benign prostatic hyperplasia. The miR-34c expression was found to inversely correlate to aggressiveness of the tumor, WHO grade, PSA levels and occurrence of metastases. Furthermore, a Kaplan-Meier analysis of patient survival based on miR-34c expression levels divided into low (< 50th percentile) and high (> 50th percentile) expression, significantly divides the patients into high risk and low risk patients (p = 0.0003, log-rank test). The phenotypic effects of miR-34c deregulation were studied in prostate cell lines, where ectopic expression of miR-34c decreased cell growth, due to both a decrease in cellular proliferation rate and an increase in apoptosis. In concordance to this, miR-34c was found to negatively regulate the oncogenes E2F3 and BCL-2, which stimulates proliferation and suppress apoptosis in PCa cells, respectively. Reversely, we could also show that blocking miR-34c in vitro increases cell growth. Further, ectopic expression of miR-34c was found to suppress migration and invasion. Our findings provide new insight into the role of miR-34c in the prostate, exhibiting tumor suppressing effects on proliferation, apoptosis and invasiveness.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
1097-0215
pubmed:author
pubmed:copyrightInfo
Copyright © 2010 UICC.
pubmed:issnType
Electronic
pubmed:day
15
pubmed:volume
127
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2768-76
pubmed:meshHeading
pubmed-meshheading:21351256-Adenocarcinoma, pubmed-meshheading:21351256-Aged, pubmed-meshheading:21351256-Aged, 80 and over, pubmed-meshheading:21351256-Apoptosis, pubmed-meshheading:21351256-Blotting, Western, pubmed-meshheading:21351256-Cell Adhesion, pubmed-meshheading:21351256-Cell Differentiation, pubmed-meshheading:21351256-Cell Movement, pubmed-meshheading:21351256-Cell Proliferation, pubmed-meshheading:21351256-Down-Regulation, pubmed-meshheading:21351256-E2F3 Transcription Factor, pubmed-meshheading:21351256-Gene Expression Regulation, Neoplastic, pubmed-meshheading:21351256-Genes, bcl-2, pubmed-meshheading:21351256-Humans, pubmed-meshheading:21351256-Immunoenzyme Techniques, pubmed-meshheading:21351256-Male, pubmed-meshheading:21351256-MicroRNAs, pubmed-meshheading:21351256-Middle Aged, pubmed-meshheading:21351256-Neoplasm Invasiveness, pubmed-meshheading:21351256-Prognosis, pubmed-meshheading:21351256-Prostatic Hyperplasia, pubmed-meshheading:21351256-Prostatic Neoplasms, pubmed-meshheading:21351256-RNA, Messenger, pubmed-meshheading:21351256-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:21351256-Tumor Cells, Cultured, pubmed-meshheading:21351256-Wound Healing
pubmed:year
2010
pubmed:articleTitle
miR-34c is downregulated in prostate cancer and exerts tumor suppressive functions.
pubmed:affiliation
Department of Laboratory Medicine, Division of Clinical Chemistry, Lund University, Malmö, Sweden.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't