Abstract
The overexpression of microRNA cluster miR-17-92 has been implicated in development of solid tumors and hematological malignancies. The role of miR-17-92 in lymphomagenesis has been extensively investigated; however, because of the developmental defects caused by miR-17-92 dysregulation, its ability to drive tumorigenesis has remained undetermined until recently. Here we demonstrate that overexpression of miR-17-92 in a limited number of hematopoietic cells is sufficient to cause B cell malignancies. In sum, our study provides a novel and physiologically relevant model that exposes the potent ability of miR-17-92 to act as a driver of tumorigenesis.
Keywords:
Lymphoma; Mouse model; miR-17-92.
Copyright © 2014 Elsevier Ltd. All rights reserved.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Blotting, Western
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Cell Proliferation
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Cell Transformation, Neoplastic / pathology*
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Gene Expression Regulation, Neoplastic*
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Hematologic Neoplasms / genetics
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Hematologic Neoplasms / metabolism
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Hematologic Neoplasms / pathology*
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Immunoenzyme Techniques
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Integrases / metabolism
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Mice
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MicroRNAs / physiology*
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Microfilament Proteins / physiology*
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Muscle Proteins / physiology*
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RNA, Messenger / genetics
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Real-Time Polymerase Chain Reaction
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Reverse Transcriptase Polymerase Chain Reaction
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Tumor Cells, Cultured
Substances
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MIRN17-92 microRNA, mouse
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MicroRNAs
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Microfilament Proteins
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Muscle Proteins
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RNA, Messenger
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Tagln protein, mouse
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Cre recombinase
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Integrases