E-GEOD-48160 - Identification of miRNA targets in breast cancer cells (DICER1 and DROSHA knockdown)

Released on 21 October 2013, last updated on 3 June 2014
Homo sapiens
Samples (6)
Array (1)
Protocols (7)
miRNAs regulate mRNA stability and translation through the action of the RNAi-induced silencing complex. In this study, we systematically identified endogenous miRNA target genes by using AGO2 immunoprecipitation (AGO2-IP) and microarray analyses in two breast cancer cell lines, MCF7 and MDA-MB-231, representing luminal and basal-like breast cancer, respectively. The expression levels of ~70% of the AGO2-IP mRNAs were increased by DROSHA or DICER1 knockdown. In addition, integrated analysis of miRNA expression profiles, mRNA-AGO2 interaction, and the 3'-UTR of mRNAs revealed that >60% of the AGO2-IP mRNAs were putative targets of the fifty most abundantly expressed miRNAs. To identify mRNAs responsive to miRNA synthesis inhibition, total RNA was prepared from control cells and cells that stably express small hairpin RNA against DICER1 or DROSHA. Expression array analysis was performed with duplicates for each cell type.
Experiment type
transcription profiling by array 
Aarti Sethuraman, Chuan H Yang, Jing Sun, Junming Yue, Lawrence M Pfeffer, Meiyun Fan, Raisa Krutilina, Zhaohui Wu
Comprehensive Analysis of MicroRNA (miRNA) Targets in Breast Cancer Cells. Fan M, Krutilina R, Sun J, Sethuraman A, Yang CH, Wu ZH, Yue J, Pfeffer LM. , Europe PMC 23921383
Investigation descriptionE-GEOD-48160.idf.txt
Sample and data relationshipE-GEOD-48160.sdrf.txt
Processed data (1)E-GEOD-48160.processed.1.zip
Additional data (1)E-GEOD-48160.additional.1.zip
Array designA-GEOD-10558.adf.txt