Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/69429
Title: Microarray and deep sequencing cross-platform analysis of the mirRNome and isomiR variation in response to epidermal growth factor
Author: Llorens, Franc
Hummel, Manuela
Pantano, Lorena
Pastor, Xavier
Vivancos, Ana
Castillo, Ester
Mattlin, Heidi
Ferrer, Anna
Ingham, Matthew
Noguera, Marc
Kofler, Robert
Dohm, Juliane C.
Pluvinet, Raquel
Bayés, Mònica
Himmelbauer, Heinz
Río Fernández, José Antonio del
Martí, Eulàlia
Sumoy, Lauro
Keywords: Factor de creixement epidèrmic
Càncer
Expressió gènica
Epidermal growth factor
Cancer
Gene expression
Issue Date: 1-Jun-2013
Publisher: BioMed Central
Abstract: BACKGROUND: Epidermal Growth Factor (EGF) plays an important function in the regulation of cell growth, proliferation, and differentiation by binding to its receptor (EGFR) and providing cancer cells with increased survival responsiveness. Signal transduction carried out by EGF has been extensively studied at both transcriptional and post-transcriptional levels. Little is known about the involvement of microRNAs (miRNAs) in the EGF signaling pathway. miRNAs have emerged as major players in the complex networks of gene regulation, and cancer miRNA expression studies have evidenced a direct involvement of miRNAs in cancer progression. RESULTS: In this study, we have used an integrative high content analysis approach to identify the specific miRNAs implicated in EGF signaling in HeLa cells as potential mediators of cancer mediated functions. We have used microarray and deep-sequencing technologies in order to obtain a global view of the EGF miRNA transcriptome with a robust experimental cross-validation. By applying a procedure based on Rankprod tests, we have delimited a solid set of EGF-regulated miRNAs. After validating regulated miRNAs by reverse transcription quantitative PCR, we have derived protein networks and biological functions from the predicted targets of the regulated miRNAs to gain insight into the potential role of miRNAs in EGF-treated cells. In addition, we have analyzed sequence heterogeneity due to editing relative to the reference sequence (isomiRs) among regulated miRNAs. CONCLUSIONS: We propose that the use of global genomic miRNA cross-validation derived from high throughput technologies can be used to generate more reliable datasets inferring more robust networks of co-regulated predicted miRNA target genes.
Note: Reproducció del document publicat a: http://dx.doi.org/10.1186/1471-2164-14-371
It is part of: Bmc Genomics, 2013, vol. 14, num. 1, p. 371
Related resource: http://dx.doi.org/10.1186/1471-2164-14-371
URI: http://hdl.handle.net/2445/69429
ISSN: 1471-2164
Appears in Collections:Articles publicats en revistes (Biologia Cel·lular, Fisiologia i Immunologia)

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