Estradiol-regulated MicroRNAs Control Estradiol Response in Breast Cancer Cells

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Estradiol-regulated MicroRNAs Control Estradiol Response in Breast Cancer Cells

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Title: Estradiol-regulated MicroRNAs Control Estradiol Response in Breast Cancer Cells
Author: Bhat-Nakshatri, Poornima; Wang, Guohua; Collins, Nikail R.; Geistlinger, Tim R.; Carroll, Jason S.; Hammond, Scott; Srour, Edward F.; Liu, Yunlong; Nakshatri, Harikrishna; Thomson, Michael J.; Brown, Myles Avery

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Citation: Bhat-Nakshatri, Poornima, Guohua Wang, Nikail R. Collins, Michael J. Thomson, Tim R. Geistlinger, Jason S. Carroll, Myles Brown, et al. 2009. Estradiol-regulated microRNAs control estradiol response in breast cancer cells. Nucleic Acids Research 37(14): 4850-4861.
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Abstract: Estradiol (E2) regulates gene expression at the transcriptional level by functioning as a ligand for estrogen receptor alpha (ERα) and estrogen receptor beta (ERβ). E2-inducible proteins c-Myc and E2Fs are required for optimal ERα activity and secondary estrogen responses, respectively. We show that E2 induces 21 microRNAs and represses seven microRNAs in MCF-7 breast cancer cells; these microRNAs have the potential to control 420 E2-regulated and 757 non-E2-regulated mRNAs at the post-transcriptional level. The serine/threonine kinase, AKT, alters E2-regulated expression of microRNAs. E2 induced the expression of eight Let-7 family members, miR-98 and miR-21 microRNAs; these microRNAs reduced the levels of c-Myc and E2F2 proteins. Dicer, a ribonuclease III enzyme required for microRNA processing, is also an E2-inducible gene. Several E2-regulated microRNA genes are associated with ERα-binding sites or located in the intragenic region of estrogen-regulated genes. We propose that the clinical course of ERα-positive breast cancers is dependent on the balance between E2-regulated tumor-suppressor microRNAs and oncogenic microRNAs. Additionally, our studies reveal a negative-regulatory loop controlling E2 response through microRNAs as well as differences in E2-induced transcriptome and proteome.
Published Version: doi:10.1093/nar/gkp500
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