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J Neurooncol ; 102(1): 19-24, 2011 Mar.
Article in English | MEDLINE | ID: mdl-20607356

ABSTRACT

MicroRNAs (miRNAs) are small noncoding RNAs comprising 21-23 nucleotides that regulate gene expression by transcriptionally repressing their complementary mRNAs. In particular, let-7 miRNA has been postulated to function as a tumor suppressor in various cancer cells, but not yet in glioblastoma. In this study, we investigated the anti-tumorigenic effect of let-7 miRNA in glioblastoma cells. Human glioblastoma cells (U251 or U87 cells) were transfected with let-7 miRNA and assayed for in-vitro proliferation, migration, and in-vivo tumor formation. Transfection of let-7 miRNA reduced expression of pan-RAS, N-RAS, and K-RAS in the glioblastoma cells. Let-7 miRNA also reduced the in-vitro proliferation and migration of the cells, and reduced the sizes of the tumors produced after transplantation into nude mice. However, let-7 miRNA exerted no effect on the proliferation of normal human astrocytes. These results indicate that let-7 miRNA has an anti-tumorigenic effect on glioblastoma cells, and suggest possible use of let-7 miRNA for treating glioblastoma.


Subject(s)
Brain Neoplasms/pathology , Cell Proliferation , Glioblastoma/pathology , MicroRNAs/physiology , Animals , Blotting, Western , Brain Neoplasms/genetics , Brain Neoplasms/metabolism , Cell Adhesion , Cell Movement , Glioblastoma/genetics , Glioblastoma/metabolism , Humans , Immunoenzyme Techniques , Male , Mice , Mice, Nude , RNA, Messenger/genetics , Reverse Transcriptase Polymerase Chain Reaction , Tumor Cells, Cultured , Xenograft Model Antitumor Assays , ras Proteins/antagonists & inhibitors , ras Proteins/genetics , ras Proteins/metabolism
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