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Cell Proliferation
Article . 2015 . Peer-reviewed
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Cell Proliferation
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miR‐454 is down‐regulated in osteosarcomas and suppresses cell proliferation and invasion by directly targeting c‐Met

Authors: Bin Li; Jianmin Sun; Guangfeng Niu; Li Sun;

miR‐454 is down‐regulated in osteosarcomas and suppresses cell proliferation and invasion by directly targeting c‐Met

Abstract

AbstractObjectivesOsteosarcoma is the most common primary bone malignancy of children and young adults. Increasing evidence has shown that microRNAs (miRNAs) are associated with cancer development, but, little is known concerning the role of miR‐454 in osteosarcoma.Materials and methodsqRT‐PCR was performed to detect expression of miR‐454 in osteosarcoma cell lines and tissues. To understand its role in osteosarcoma, we reintroduced expression of miR‐454 in the MG‐63 cell line by transfection with miR‐454 mimics or inhibitors. CCK‐8 assay and an invasion assay were used to detect the functional role of miR‐454. Luciferase assay and western blot analysis were performed to detect the target gene of miR‐454.ResultsmiR‐454 was found to be down‐regulated in osteosarcoma tissues and cell lines. Its over‐expression inhibited tumour growth and invasion and its down‐regulation promoted cell proliferation and invasion. Subsequent investigation revealed that c‐Met was a direct and functional target of miR‐454 in osteosarcoma. Overexpression of miR‐454 impaired c‐Met‐induced cell proliferation and invasion. Finally, miR‐454 was found to be inversely correlated to c‐Met expression in human osteosarcoma tissues.ConclusionsReduced‐expression of miR‐454 in osteosarcoma cells promoted tumour growth by targeting c‐Met, thus miR‐454 may be a potential therapy target for this tumour.

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Keywords

Adult, Osteosarcoma, Binding Sites, Bone Neoplasms, Proto-Oncogene Proteins c-met, Transfection, Gene Expression Regulation, Neoplastic, MicroRNAs, Cell Movement, Genes, Reporter, Cell Line, Tumor, Humans, Child, Luciferases, Cell Proliferation, Plasmids, Signal Transduction

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    Impact byBIP!
    citations
    This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    63
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 10%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Top 10%
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 1%
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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
63
Top 10%
Top 10%
Top 1%
gold
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Cancer Research