Source:http://linkedlifedata.com/resource/pubmed/id/19137007
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
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pubmed:dateCreated |
2009-3-12
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pubmed:abstractText |
Dysregulated expression of microRNAs (miRNAs) is associated with a variety of diseases, including colorectal cancer. By comparing more than 200 miRNAs in 13 pairs of matched colorectal cancer and normal adjacent tissue samples through qRT-PCR and microarray analysis, we found a widespread disruption of miRNA expression during colorectal tumorigenesis. In particular, among a panel of presumed targets generated by in silico analysis that may interact with these aberrantly expressed miRNAs, KRAS oncogene has been further experimentally validated as the target of miR-143. First, an inverse correlation between KRAS protein and miR-143 in vivo was found. Second, KRAS expression in Lovo cells was significantly abolished by treatment with miR-143 mimic, whereas miR-143 inhibitor increased KRAS protein level. Third, luciferase reporter assay confirmed that miR-143 directly recognize the 3'-untranslated region of KRAS transcripts. Four, Lovo cells treated with miR-143 inhibitor showed a stimulated cell proliferation, whereas miR-143 overexpression had an opposite effect. Finally, inhibition of KRAS expression by miR-143 inhibits constitutive phosphorylation of ERK1/2. Taken together, the present study provides the first evidences that miR-143 is significant in suppressing colorectal cancer cell growth through inhibition of KRAS translation.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1476-5594
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pubmed:author |
pubmed-author:CauDD,
pubmed-author:ChenJJ,
pubmed-author:ChewAA,
pubmed-author:GuyRR,
pubmed-author:PaiP NPN,
pubmed-author:RekYY,
pubmed-author:WandHH,
pubmed-author:WangGG,
pubmed-author:WangJJ,
pubmed-author:XiangYY,
pubmed-author:YangRR,
pubmed-author:YinYY,
pubmed-author:ZenKK,
pubmed-author:ZhangC-YCY,
pubmed-author:ZhangHH,
pubmed-author:ZhangJJ,
pubmed-author:ZhangYY,
pubmed-author:ZinTT
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pubmed:issnType |
Electronic
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pubmed:day |
12
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pubmed:volume |
28
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1385-92
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pubmed:meshHeading |
pubmed-meshheading:19137007-Colorectal Neoplasms,
pubmed-meshheading:19137007-Genes, Tumor Suppressor,
pubmed-meshheading:19137007-Humans,
pubmed-meshheading:19137007-MicroRNAs,
pubmed-meshheading:19137007-Oligonucleotide Array Sequence Analysis,
pubmed-meshheading:19137007-Proto-Oncogene Proteins,
pubmed-meshheading:19137007-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:19137007-ras Proteins
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pubmed:year |
2009
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pubmed:articleTitle |
Role of miR-143 targeting KRAS in colorectal tumorigenesis.
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pubmed:affiliation |
Jiangsu Diabetes Center, State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, Jiangsu, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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