MCB
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Other Versions of this Article:
MCB.00242-06v1
26/21/8191    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hossain, A.
Right arrow Articles by Saunders, G. F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hossain, A.
Right arrow Articles by Saunders, G. F.
Molecular and Cellular Biology, November 2006, p. 8191-8201, Vol. 26, No. 21
0270-7306/06/$08.00+0     doi:10.1128/MCB.00242-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

Mir-17-5p Regulates Breast Cancer Cell Proliferation by Inhibiting Translation of AIB1 mRNA{triangledown}

Anwar Hossain,1* Macus T. Kuo,2 and Grady F. Saunders1,{dagger}

Department of Biochemistry and Molecular Biology, The University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77030,1 Department of Molecular Pathology, The University of Texas M. D. Anderson Cancer Center, 7435 Fannin Street, Houston, Texas 770542

Received 8 February 2006/ Returned for modification 3 April 2006/ Accepted 15 August 2006

MicroRNAs are an extensive family of ~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.


* Corresponding author. Mailing address: Department of Molecular Pathology, Unit 89, The University of Texas M. D. Anderson Cancer Center, 7435 Fannin Street, Houston, TX 77054. Phone: (713) 834-6079. Fax: (713) 834-6084. E-mail: ahossain{at}mdanderson.org.

{triangledown} Published ahead of print on 28 August 2006.

{dagger} Deceased.


Molecular and Cellular Biology, November 2006, p. 8191-8201, Vol. 26, No. 21
0270-7306/06/$08.00+0     doi:10.1128/MCB.00242-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
J. Bacteriol. J. Virol. Eukaryot. Cell
Microbiol. Mol. Biol. Rev. Clin. Vaccine Immunol. All ASM Journals

Copyright © 2006 by the American Society for Microbiology. All rights reserved.