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Mol Cell Biol. 2006 Nov;26(21):8191-201. Epub 2006 Aug 28.

Mir-17-5p regulates breast cancer cell proliferation by inhibiting translation of AIB1 mRNA.

Author information

1
Department of Biochemistry and Molecular Biology, The University of Texas M. D. Anderson Cancer Center, Houston, TX 77054, USA. ahossain@mdanderson.org

Abstract

MicroRNAs are an extensive family of approximately 22-nucleotide-long noncoding RNAs expressed in a wide range of eukaryotes, including humans, and they are important in development and disease. We found that microRNA Mir-17-5p has extensive complementarity to the mRNA of AIB1 (named for "amplified in breast cancer 1"). Cell culture experiments showed that AIB1 expression was downregulated by Mir-17-5p, primarily through translational inhibition. Expression of Mir-17-5p was low in breast cancer cell lines. We also found that downregulation of AIB1 by Mir-17-5p resulted in decreased estrogen receptor-mediated, as well as estrogen receptor-independent, gene expression and decreased proliferation of breast cancer cells. Mir-17-5p also completely abrogated the insulin-like growth factor 1-mediated, anchorage-independent growth of breast cancer cells. Our results reveal that Mir-17-5p has a role as a tumor suppressor in breast cancer cells.

PMID:
16940181
PMCID:
PMC1636750
DOI:
10.1128/MCB.00242-06
[Indexed for MEDLINE]
Free PMC Article

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