Faculty, Staff and Student Publications

Publication Date

1-1-2017

Journal

Cancer Discovery

DOI

10.1038/celldisc.2017.29

PMID

28904816

PMCID

PMC5594916

PubMedCentral® Posted Date

9-12-2017

PubMedCentral® Full Text Version

Post-print

Abstract

The regulation of microRNA (miRNA) biogenesis, function and degradation involves a range of mechanisms, including interactions with RNA-binding proteins. The potential contribution of regulatory miRNAs to the expression of these RNA interactor proteins that could control other miRNAs expression is still unclear. Here we demonstrate a regulatory circuit involving oncogenic and tumor-suppressor miRNAs and an RNA-binding protein in a chemotherapy-resistant ovarian cancer model. We identified and characterized miR-15a-5p and miR-25-3p as negative regulators of hnRNPA1 expression, which is required for the processing of miR-18a-3p, an inhibitor of the

Keywords

chemotherapy resistance, hnRNPA1, K-RAS, microRNAs, ovarian cancer, RNA-binding proteins

Comments

This article has been corrected. See Cell Discov. 2023 Nov 8;9:111.

Published Open-Access

yes

41421_2023_Article_611.pdf (401 kB)
Correction

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