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Cited by 580

The DOI matches its Crossref record; 40 of the 40 references it cites were found in a registry or an index.

miR-24 Inhibits Cell Proliferation by Targeting E2F2, MYC, and Other Cell-Cycle Genes via Binding to “Seedless” 3′UTR MicroRNA Recognition Elements

Open access
Lal, Ashish, Navarro, Francisco, Maher, Christopher A., Maliszewski, Laura E., Yan, Nan, O'Day, Elizabeth, Chowdhury, Dipanjan, Dykxhoorn, Derek M., Tsai, Perry, Hofmann, Oliver, Becker, Kevin G., Gorospe, Myriam, Hide, Winston, Lieberman, Judy·2009·Molecular Cell

Abstract

Summary miR-24, up-regulated during terminal differentiation of multiple lineages, inhibits cell cycle progression. Antagonizing miR-24 restores post-mitotic cell proliferation and enhances fibroblast proliferation, while over-expressing miR-24 increases the G1 compartment. The 248 mRNAs down-regulated upon miR-24 over-expression are highly enriched for DNA repair and cell cycle regulatory genes that form a direct interaction network with prominent nodes at genes that enhance (MYC, E2F2, CCNB1, CDC2) or inhibit (p27Kip1, VHL) cell cycle progression. miR-24 directly regulates MYC and E2F2 and some genes they transactivate. Enhanced proliferation from antagonizing miR-24 is abrogated by knocking down E2F2, but not MYC, and cell proliferation, inhibited by miR-24 over-expression, is rescued by miR-24-insensitive E2F2. Therefore, E2F2 is a critical miR-24 target. The E2F2 3′UTR lacks a predicted miR-24 recognition element. In fact, miR-24 regulates expression of E2F2, MYC, AURKB, CCNA2, CDC2, CDK4 and FEN1 by recognizing seedless, but highly complementary, sequences.

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Crossref · 10.1016/j.molcel.2009.08.020

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Metadata

Authors
Lal, A., Navarro, F., Maher, C. A., Maliszewski, L. E., Yan, N., O'Day, E., Chowdhury, D., Dykxhoorn, D. M., Tsai, P., Hofmann, O., Becker, K. G., Gorospe, M., Hide, W., & Lieberman, J.
Venue
Molecular Cell
Publisher
Elsevier BV
Published
2009-09
Volume
35
Issue
5
Pages
610-625
ISSN
1097-2765 (ISSN-L)
OpenAlex
W2051126469
Cited by
580
References
40
FWCI
16.71
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: miR-24 Inhibits Cell Proliferation by Targeting E2F2, MYC, and Other Cell-Cycle Genes via Binding to “Seedless” 3′UTR MicroRNA Recognition Elements. https://app.cochat.ai/papers/10.1016/j.molcel.2009.08.020
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Lal, A., Navarro, F., Maher, C. A., Maliszewski, L. E., Yan, N., O'Day, E., Chowdhury, D., Dykxhoorn, D. M., Tsai, P., Hofmann, O., Becker, K. G., Gorospe, M., Hide, W., & Lieberman, J. (2009). miR-24 Inhibits Cell Proliferation by Targeting E2F2, MYC, and Other Cell-Cycle Genes via Binding to “Seedless” 3′UTR MicroRNA Recognition Elements. Molecular Cell. https://doi.org/10.1016/j.molcel.2009.08.020

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.