Synchronous down-modulation of miR-17 family members is an early causative event in the retinal angiogenic switch
Year: 2015
Type: article
Abstract: Six members of the microRNA-17 (miR-17) family were mapped to three different chromosomes, although they share the same seed sequence and are predicted to target common genes, among which are those encoding hypoxia-inducible factor-1α (HIF1A) and VEGFA. Here, we evaluated the in vivo expression profile of the miR-17 family in the murine retinopathy of prematurity (ROP) model, whereby Vegfa expression is highly enhanced at the early stage of retinal neovascularization, and we found simultaneous reduction of all miR-17 family members at this stage. Using gene reporter assays, we observed binding of these miRs to specific sites in the 3' UTRs of Hif1a and Vegfa. Furthermore, overexpression of these miRs decreased HIF1A and VEGFA expression in vitro. Our data indicate that this miR-17 family elicits a regulatory synergistic down-regulation of Hif1a and Vegfa expression in this biological model. We propose the existence of a coordinated regulatory network, in which diverse miRs are synchronously regulated to target the Hif1a transcription factor, which in turn, potentiates and reinforces the regulatory effects of the miRs on Vegfa to trigger and sustain a significant physiological response.
Authors: Diana N. Nunes, Emmanuel Dias-Neto, Marina Cardó-Vila, Julianna K. Edwards, Andrey S. Dobroff, Ricardo J. Giordano, Jami Mandelin, Helena P. Brentani, Catrin Hasselgren, Virginia J. Yao, Serena Marchiò, Carlos A. B. Pereira, Fabio Passetti, George A. Calin, Richard L. Sidman, Wadih Arap, Renata Pasqualini
Institutions: AC Camargo Hospital, Universidade de São Paulo, UNM Comprehensive Cancer Center, University of New Mexico, Instituto Nacional de Câncer - INCA, Candiolo Cancer Institute, University of Turin, The University of Texas MD Anderson Cancer Center, Beth Israel Deaconess Medical Center, Harvard University
Language: English
Subfield: Cancer Research
Domain: Life Sciences
Open Access status: green
Funder: National Eye Institute
Award: G6267034380
OpenAlex ID: W1995340861
