He, L., He, X., Lowe, S. W., Hannon, G. J.
(November 2007)
microRNAs join the p53 network - another piece in the tumour-suppression puzzle.
Nat Rev Cancer, 7 (11).
pp. 819-822.
ISSN 1474-1768 (Electronic)
Abstract
Several recent studies have found a conserved microRNA (miRNA) family, the miR-34s, to be direct transcriptional targets of p53. miR-34 activation can recapitulate elements of p53 activity, including induction of cell-cycle arrest and promotion of apoptosis, and loss of miR-34 can impair p53-mediated cell death. These data reinforce the growing awareness that non-coding RNAs are key players in tumour development by placing miRNAs in a central role in a well-known tumour-suppressor network.
Item Type: |
Paper
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Subjects: |
diseases & disorders > cancer bioinformatics > genomics and proteomics > genetics & nucleic acid processing > DNA, RNA structure, function, modification > transcription bioinformatics > genomics and proteomics > genetics & nucleic acid processing > DNA, RNA structure, function, modification > miRNA bioinformatics > genomics and proteomics > genetics & nucleic acid processing > DNA, RNA structure, function, modification > miRNA bioinformatics > genomics and proteomics > genetics & nucleic acid processing > DNA, RNA structure, function, modification > genes, structure and function > genes: types > miR-34 bioinformatics > genomics and proteomics > genetics & nucleic acid processing > DNA, RNA structure, function, modification > genes, structure and function > genes: types > p53 |
CSHL Authors: |
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Communities: |
CSHL labs > Hannon lab CSHL labs > Lowe lab |
Depositing User: |
CSHL Librarian
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Date: |
November 2007 |
Date Deposited: |
15 Nov 2011 15:29 |
Last Modified: |
02 Dec 2016 15:52 |
PMCID: |
PMC4053212 |
Related URLs: |
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URI: |
https://repository.cshl.edu/id/eprint/23031 |
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